Cranberry Pomegranate Synbiotic
Bladder and Prostate Health
The advanced Cranberry Pomegranate Synbiotic formula is a marvel for UTI care.*
Higher potency concentrates of organic cranberries and extracts of pomegranates are combined with BioImmersion’s renowned Super Blend of naturally occurring whole probiotic organism, expertly grown to retain their Supernatant and ORNs (oligoribonucleotides). The advanced formula is a powerhouse of goodness for urinary tract infections, and an effective agent for bladder, prostate, and kidney health.*
The Super Blend in the Cranberry Pomegranate formula has 30 billion CFU per gram.
The formula is organic, vegan, Kosher, Non GMO, and Gluten free.
- Description
- Research
- Ingredients
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Protocol
Urinary tract infection (UTI) is one of the most common bacterial infections (Foxman, 2014), often caused by Gram-negative bacteria, enterobacteriaceae (Bader, Loeb & Brooks, 2017), and more specifically within this large bacterial family, the familiar Escherichia coli (Jensen et al., 2017). In recent years, more women suffer from chronic UTIs due to the climbing rise of antibiotic resistant bacteria. As a natural alternative or a supportive adjunct treatment with antibiotics, the Cranberry Pomegranate Synbiotic Formula offers well-researched phyto nutrients, probiotics, prebiotics, and D- mannose. Studies and clinical trials find cranberries (Bader et al., 2017; Jensen et al., 2017; de Llano et al., 2015), Pomegranates (Pagliarulo et al., 2016; Heber, 2011; Duman et al., 2009), along with probiotics, prebiotics, and D- mannose (Spaulding et al., 2017; 2017a; Domenici et al., 2016), to offer effective management and support for UTI.*
Historically, cranberries and cranberry juice have long been used to alleviate urinary tract infections, with research linking the ability of cranberries’ proanthocyanidins (Krueger et al., 2013) to inhibit adhesion of E. coli bacteria (Neto, 2007). As early as 1933, research by Fellers et al. has shown cranberries to positively effect urinary health. Cowan’s (1999) seminal work on plant products as antimicrobial agents, which includes cranberries, has been cited in approximately 7,500 research articles. Studies on cranberries show not only an alternative to antibiotic but also as a daily supplement for a steady prevention of UTIs.*
Recent studies continue to observe and explain cranberries’ excellent antimicrobial properties, especially the phenol elements and mechanism that are beneficial for the management and prevention of UTI (Jensen et al., 2017; Rodríguez-Pérez et al., 2017; Baranowska & Bartoszek, 2016; Sagdic et al, 2006; Lee, 2000). As stated above, proanthocyanidins in cranberries are found to prevent the adherence of Escherichia coli to uroepithelial cells in the urinary tract (Sun et al., 2015; Rowley, 2012; Burger et al., 2000), and disrupt hard to treat biofilm-mediated infections caused by Pseudomonas aeruginosa (Ulrey et al., 2014).*
Cranberries also pack other antimicrobial, antioxidant and anti-inflammatory benefits. With their powerful anti-adhesion properties, cranberries are found to inhibit growth of Helicobacter Pylori (Shmuely et al., 2007; Zhang et al., 2005; Burger et al., 2002), suppress tumor cell proliferation and offer support during cancer treatment (Bshayee et al., 2016; Kresty et al., 2015), as well as lower markers of cardio-metabolic risk (Novotny et al., 2015), and enhance the GI’s microbiota (Blumberg et al., 2016). Cranberries are shown to be effective agents for health.*
Pomegranate has enjoyed an exalted status since ancient times, and no wonder (Parseh et al., 2012). Studies show pomegranates contain 124 different phyto-nutrients with curative and preventative qualities. The pomegranate fruit is actually considered a berry, or more accurately, each pomegranate contains 600 seeds, each surrounded by fleshy white to dark red pulp (Rahimi et al., 2012).*
With their potent polyphenolic flavonoids, pomegranates show higher concentrations of antioxidants than green tea (Noda et al., 2002; Nori-Okamoto et al., 2004), cranberries, apples, grapes, or pears (Hmid et al., 2017; Heber, 2011; Heber et al., 2006). The pomegranate’s high concentration of polyphenols wields an inhibitory effect on pathogenic Staphylococcus aureus and Escherichia coli, serving as natural antimicrobial agents (Pagliarulo et al., 2016; Naz et al., 2007; Voravuthikunchai et al., 2005). Other microbial organisms are shown to be sensitive to the pomegranate phenolic flavonoids. Nascimento et al. (2000) tested extracts from a variety of plants in search of a natural support against antibiotic resistant microorganisms and found the pomegranate to be especially effective against Pseudomonas aeruginosa. Machado et al. (2002) identified antimicrobial ellagitannin of the pomegranate to be valuable to treat methicillin-resistant Staphylococcus aureus (MRSA) strains.*
Similarly, the pomegranate’s antioxidants work as scavengers and metal chelators (Kulkarni et al., 2007). The antioxidant, antimalarial, and antimicrobial activities of the tannin-rich fractions, ellagitannins and phenolic acids from pomegranates offer excellent daily dietary food supplement to enhance the immune system (Reddy et al., 2007).*
Probiotics and Supernatant are important to the health of our urogenital system. The genus Lactobacillus has been studied for their promising preventative and/or treatment potential against UTIs (de Llano et al., 2017). Three strains of lactobacillus were tested for their capabilities to inhibit pathogenic adherence of E. coli, E. faecalis, and Staphylococcus epidermidis to T24 epithelial bladder cells. L. salivarious, L. acidophilus showed a significantly inhibited the adherence of pathogens (de Llano et al., 2017; see also Shim et al., 2016). Lactobacillus species were also studies with infants experiencing acute pyelonephritis [kidney infection], and found effective in the prevention of urinary tract infections (Lee et al., 2016).*
The “anti-infective activities” of lactobacillus strains are exhibiting a great promise as innovative anti-infectious agents (Liévin-Le Moal et al., 2014), and especially for recurrent UTIs (Manzoor et al., 2016).*
Depletion of vaginal Lactobacilli has also found in research to be linked with UTI risk, which suggests that repletion (re-colonization of Lactobacilli) might be beneficial (Syngai et al., 2016; Fontana et al., 2013; Maurya et al., 2014).*
Supernatant is the fermented medium crated during the culturing process of probiotics. Supernatant is the fermented “soup” that contains important probiotic metabolites which is comprised of enzymes, peptides, proteins, vitamins, and other nutrients and factors, including antimicrobials such as bacitracins. Supernatant is shown in research to have powerful antimicrobial properties with the potential to block adhesion, invasion and translocation of E. coli, yet it is gentle enough to be used to ‘enhance neonatal resistance to systemic Escherichia coli K1 infection by accelerating development of intestinal defense’ (He et al., 2017). In fact, Lazar et al. (2009) in vitro study concluded that the soluble probiotic metabolites, or supernatant, might actually interfere with the beginning stages of adherence and colonization of selected E. coli. This means that the supernatant itself exudes protective effects (Lazar et al., 2009), as well as work synergistically with probiotics organism to stimulate the immune system against pathogenic invasion (Ditu et al., 2014).*
D-mannose has long shown an ability to support acute UTIs, inhibiting bacterial adhesion to the urothelium (Domenici et al., 2016; Kranjčec et al., 2014). Testing more sensitive populations, such as people with multiple sclerosis (MS) who suffer from recurrent UTIs, showed that D-mannose effected a reduction in the number of UTIs as well as reduction for the need of antibiotics (Panicker et al., 2016).*
Since 150 million people suffer from UTIs annually, using natural foods and nutriceutical agents to combat recurrence of UTI infections is advisable (Spaulding et al., 2017). The use of cranberries, pomegranates, probiotics, supernatant, and D-mannose form a potent synergistic effect that is shown in research to be very effective (Vicarotto, 2014).*
There are many more health functions that cranberries and pomegranates perform. For many years cranberries and pomegranates were studied to understand their anti-tumorigenic elements (e.g., Castonguay et al., 1997). More recent studies continue to reveal and explain the bioactivity of pomegranate (Panth et al., 2017; Bishayee et al., 2016; Faria & Calhau, 2011) and cranberries (Kresty et al., 2015; Hochman et al., 2008; Ferguson et al., 2006) as promising suppressants and inhibitors of different kinds of cancer cells (Weh et al., 2016; Liberty et al., 2009; Adams et al., 2006).*
And there is more: Research studies find pomegranate and cranberries phenolics to contribute to heart health (Taheri et al., 2017; Novotny et al., 2015; Aviram et al., 2008, 2002), to balance the gut microbiota (Blumberg et al., 2016), and to offer liver support (Bishayee et al., 2013, 2011). Check the Research Tab for more in depth studies.*
The Cranberry Pomegranate Synbiotic Formula is an excellent choice for UTIs. Cranberries, Pomegranates, Probiotics, supernatant, and D-mannose have all shown in research to provide a potent effect against UTIs. The combination of these ingredients offers a promising natural supplement to prevent and maintain a healthy balance of the urogenital system. We suggest 2-4 capsules twice daily for UTI management, and 1-2 capsules daily for preventative support.*
REFERENCES
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Cowan, M. M. (1999). Plant products as antimicrobial agents. Clinical microbiology reviews, 12(4), 564-582. Abstract
de Llano, D. G., Arroyo, A., Cárdenas, N., Rodríguez, J. M., Moreno-Arribas, M., & Bartolomé, B. (2017). Strain-specific inhibition of the adherence of uropathogenic bacteria to bladder cells by probiotic Lactobacillus spp. Pathogens and Disease, 75(4). DOI:10.1093/femspd/ftx043
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Spaulding, C. N., Klein, R. D., Ruer, S., Kau, A. L., Schreiber, H. L., Cusumano, Z. T., ... & Remaut, H. (2017). Selective depletion of uropathogenic E. coli from the gut by a FimH antagonist. Nature, 546(7659), 528-532. DOI:10.1038/nature22972
Spaulding, C. N., Kau, A. L., Klein, R. D., Janetka, J. W., Gordon, J. I., & Hultgren, S. J. (2017a). Small-molecule inhibitors against type 1 pili selectively target uropathogenic E. coli in the gut and bladder. The FASEB Journal, 31(1 Supplement), 939-9. Abstract
Sun, J., Marais, J. P., Khoo, C., LaPlante, K., Vejborg, R. M., Givskov, M., ... & Rowley, D. C. (2015). Cranberry (Vaccinium macrocarpon) oligosaccharides decrease biofilm formation by uropathogenic Escherichia coli. Journal of functional foods, 17, 235-242. DOI:10.1016/j.jff.2015.05.016
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Vicariotto, F. (2014). Effectiveness of an association of a cranberry dry extract, D-mannose, and the two microorganisms Lactobacillus plantarum LP01 and Lactobacillus paracasei LPC09 in women affected by cystitis: a pilot study. Journal of clinical gastroenterology, 48, S96-S101. DOI:10.1097/MCG.0000000000000224
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FOOD SCIENCE: THE APPLICATION AND USE OF CRANBERRY, POMEGRANATE, PROBIOTICS (BULGARIAN ORIGIN), SUPERNATANT, D-MANNOSE, AND CHICORY SOLUBLE FIBER.*
Historical and Clinical Reviews of Cranberries and Pomegranate
Heber, D. (2011). Pomegranate Ellagitannins. In I.F.F., Benzie, & S. Wachtel-Galor (Eds.), Herbal medicine: Biomolecular and clinical aspects. 2nd edition. Boca Raton, FL: CRC Press/Taylor & Francis. https://www.ncbi.nlm.nih.gov/books/NBK92772/
Neto, C.C., & Vinson, J.A. (2011). Cranberry. In I.F.F., Benzie, & S. Wachtel-Galor (Eds.), Herbal medicine: Biomolecular and clinical aspects. 2nd edition. Boca Raton, FL: CRC Press/Taylor & Francis. https://www.ncbi.nlm.nih.gov/books/NBK92771/
Usta, C., Ozdemir, S., Schiariti, M., & Puddu, P. E. (2013). The pharmacological use of ellagic acid-rich pomegranate fruit. International journal of food sciences and nutrition, 64 (7), 907-913. DOI: 10.3109/09637486.2013.798268
Cranberries : UTI Support and Management
Avorn, J., Monane, M., Gurwitz. J.H., Glynn. R.J., Choodnovskiy, I., Lipsitz, L.A. (1994). Reduction ofbacteriuria and pyuria after ingestion of cranberry juice. J Am Med Assoc, 271, 751–4. doi:10.1001/jama.1995.03510340041031
Bailey, D.T., Dalton, C., Daugherty, F.J., & Tempesta, M.S. (2007). Can a concentrated cranberry extract prevent recurrent urinary tract infections in women? A pilot study. Phytomed, 14, 237–41. DOI: 10.1016/j.phymed.2007.01.004
Bader, M. S., Loeb, M., & Brooks, A. A. (2017). An update on the management of urinary tract infections in the era of antimicrobial resistance. Postgraduate medicine, 129(2), 242-258. http://dx.doi.org/10.1080/00325481.2017.1246055
Cowan, M. M. (1999). Plant products as antimicrobial agents.Clinical microbiology reviews, 12(4), 564-582. Abstract
Davidson, E., Zimmermann, B.F., Jungfer, E., & Chrubasik-Hausmann, S. (2014). Prevention of Urinary Tract Infections with Vaccinium Products. Phytotherapy Research, 28, (3), 465-470. DOI: 10.1002/ptr.5047
de Llano, D.G., Esteban-Fernández, A., Sánchez-Patán, F., Martínlvarez, P.J., Moreno-Arribas, M.V., Bartolomé, B. (2015). Anti-Adhesive Activity of Cranberry Phenolic Compounds and Their Microbial-Derived Metabolites against Uropathogenic Escherichia coli in Bladder Epithelial Cell Cultures.Int J Mol Sci, 16(6), 12119-30. DOI: 10.3390/ijms160612119
Di Martino, P., Agniel, R., David, K., Templer, C., Gaillard, J.L., Denys, P., & Botto, H. (2006). Reduction of Escherichia coli adherence to uroepithelial bladder cells after consumption of cranberry juice: A double-blind,randomized placebo-controlled cross-over trial. WorldJ Urol, 24, 21–7. DOI: 10.1007/s00345-005-0045-z
Ermel, G., Georgeault, S., Inisan, C., Besnard, M. (2012). Inhibition of adhesion of uropathogenic Escherichia coli bacteria to uroepithelial cells by extracts from cranberry. J Med Food, 15(2):126-34. DOI: 10.1089/jmf.2010.0312
Feliciano, R.P., Krueger, C.G., Reed, J.D. (2015). Methods to determine effects of cranberry proanthocyanidins on extraintestinal infections: Relevance for urinary tract health. Mol Nutr Food Res, 59 (7), 1292-306. DOI: 10.1002/mnfr.201500108
Fleet, J.C. (1994). New support for a folk remedy: cranberry juice reduces bacteriuria and pyuria in elderly women. Nutr Rev, 52(5),168-70. DOI:10.1111/j.1753-4887.1994.tb01413.x
Foo, L.Y., Lu, Y., Howell, A.B., & Vorsa, N. (2000). The structure of cranberry proanthocyanidins which inhibit adherence of uropathogenic P-fimbriated Escherichia coli in vitro. Phytochemistry, 54(2), 173-81. https://doi.org/10.1016/S0031-9422(99)00573-7
Foxman, B., Cronewett, A.E.W., Spino, C., Berger, M.B., Morgan, D.M. (2015). Cranberry juice capsules and urinary tract infection after surgery: results of a randomized trial. American Journal of Obstetrics and Gynecology, 213(2), 123-124. DOI: 10.1016/j.ajog.2015.04.003
Foxman B. (2014). Urinary tract infection syndromes: occurrence, recurrence, bacteriology, risk factors, and disease burden. Infect. Dis. Clin. North. Am. 28, 1–13. DOI: 10.1016/j.idc.2013.09.003
Gupta, A., Dwivedi, M., Mahdi, A.A., Nagana Gowda, G.A., Khetrapal, C.L., Bhandari, M. (2012). Inhibition of adherence of multi-drug resistant E. coli by proanthocyanidin. Urol Res, 40(2), 143-50. DOI: 10.1007/s00240-011-0398-2
Gupta, K., Chou, M.Y., Howell, A., Wobbe, C., Grady, R., Stapleton, A.E. (2007). Cranberry products inhibit adherence of p-fimbriated Escherichia coli to primary cultured bladder and vaginal epithelial cells. J Urol, 177(6), 2357-60. DOI: 10.1016/j.juro.2007.01.114
Hisano, M., Bruschini, H., Nicodemo, A.C., & Srougi, M. (2012). Cranberries and lower urinary tract infection prevention. CLINICS, 67(6), 661-667. doi: 10.6061/clinics/2012(06)18
Howell, A., Souza, D., Roller, M., Fromentin, E. (2015). Comparison of the Anti-Adhesion Activity of Three Different Cranberry Extracts on Uropathogenic P-fimbriated Escherichia coli: a Randomized, Double-blind, Placebo Controlled, Ex Vivo, Acute Study. Nat Prod Commun. 2015 Jul; 10(7):1215-8. Abstract
Howell, A.B., Botto, H., Combescure, C., Blanc-Potard, A.B., Gausa, L., Matsumoto, T., … Lavigne, J.P. (2010). Dosage effect on uropathogenic Escherichia coli anti-adhesion activity in urine following consumption of cranberry powder standardized for proanthocyanidin content: a multicentric randomized double blind study. BMC Infect Dis, 10, 95. doi: 10.1186/1471-2334-10-94 .
Howell A. (2002). Cranberry proanthocyanidins and the maintenance of urinary tract health. Crit Rev Food Sci Nutr; 42S, 273–8. DOI: 10.1080/10408390209351915
Howell A.B, Vorsa N, Der Marderosian A, Foo L.Y. (1998). Inhibition of the adherence of P-fimbriated Escherichia coli to uroepithelial-cell surfaces by proanthocyanidin extracts from cranberries. N Eng J Med, 339,1085–6. DOI: 10.1056/NEJM199810083391516
Jensen, H.D., Carsten, S., Christensen, S.B., & Krogfelt, K.A. (2017). Cranberry juice and combinations of its organic acids are effective against experimental urinary tract infection. Front Microbiol, 8, 542. doi: 10.3389/fmicb.2017.00542
Kaspar, K.L., Howell, A.B., & Khoo, C. (2015). A randomized, double-blind, placebo-controlled trial to assess the bacterial anti-adhesion effects of cranberry extract beverages.Food Funct, 6(4), 1212-7. DOI: 10.1039/c4fo01018c
Krueger, C. G., Reed, J. D., Feliciano, R. P., & Howell, A. B. (2013). Quantifying and characterizing proanthocyanidins in cranberries in relation to urinary tract health. Analytical and bioanalytical chemistry, 405(13), 4385-4395. DOI: 10.1007/s00216-013-6750-3
Liu, Y., Pinzón-Arango, P.A., Gallardo-Moreno, A.M., Camesano, T.A. (2010). Direct adhesion force measurements between E. coli and human uroepithelial cells in cranberry juice cocktail. Mol Nutr Food Res, 54(12), 1744-52. DOI: 10.1002/mnfr.200900535
Liu, Y., Gallardo-Moreno, A.M., Pinzon-Arango, P.A., Reynolds, Y., Rodriguez, G., Camesano TA. (2008). Cranberry changes the physicochemical surface properties of E. coli and adhesion with uroepithelial cells. Colloids Surf B Biointerfaces, 65(1), 35-42. DOI: 10.1016/j.colsurfb.2008.02.012
Liu, Y., Black, M.A., Caron, L., Camesano, T.A. (2006). Role of cranberry juice on molecular-scale surface characteristics and adhesion behavior of Escherichia coli. Biotechnol Bioeng, 93(2), 297-305. DOI: 10.1002/bit.20675
Margetis, D., Roux, D., Gaudry, S., Messika, J., Bouvet, O., Branger, C….Ricard, J.D. (2015). Effects of Proanthocyanidins on Adhesion, Growth, and Virulence of Highly Virulent Extraintestinal Pathogenic Escherichia coli Argue for Its Use to Treat Oropharyngeal Colonization and Prevent Ventilator-Associated Pneumonia. Crit Care Med, 43(6), e170-8. DOI: 10.1097/CCM.0000000000000972
Mathers, M.J., von Rundstedt, F., Brandt, A.S., Koig, M., Lazica, D.A., & Roth, S. (2009). [Myth or truth. Cranberry juice for prophylaxis and treatment of recurrent urinary tract infection]. Urologe A, 48 (10), 1203-9. [Article in German]. DOI: 10.1007/s00120-009-2051-z
Mathison, B.D., Kimble, L.L., Kaspar, K.L., Khoo, C., Chew, B.P. (2014). Consumption of cranberry beverage improved endogenous antioxidant status and protected against bacteria adhesion in healthy humans: a randomized controlled trial. Nutr Res, 34(5), 420-7. DOI: http://dx.doi.org/10.1016/j.nutres.2014.03.006
McMurdo, M.E., Argo, I., Phillips, G., Daly, F., & Davey, P. (2009). Cranberry or trimethoprim for the prevention of recurrent urinary tract infections? A randomized controlled trial in older women.J Antimicrob Chemother, 63, 389–95. DOI: 10.1093/jac/dkn489
McMurdo, M.E., Bissett, L.Y., Price, R.J., Phillips, G., & Crombie, I.K. (2005). Does ingestion of cranberry juice reduce symptomatic urinary tract infections in older people in hospital? A double-blind, placebo-controlled trial. Age Ageing, 34(3), 256-61. DOI: 10.1093/ageing/afi101
Nicolosi, D., Tempera, G., Genovese, C., Furneri, P.M. (2014). Anti-Adhesion Activity of A2-type Proanthocyanidins (a Cranberry Major Component) on Uropathogenic E. coli and P. mirabilis Strains. Antibiotics (Basel), 3(2), 143-54. doi: 10.3390/antibiotics3020143
Pérez-López, F.R., Haya, J., Chedraui, P. (2009). Vaccinium macrocarpon: an interesting option for women with recurrent urinary tract infections and other health benefits. J Obstet Gynaecol Res, 35(4), 630-9. DOI: 10.1111/j.1447-0756.2009.01026.x
Pinzón-Arango, P.A., Liu, Y., Camesano, T.A. (2009). Role of cranberry on bacterial adhesion forces and implications for Escherichia coli-uroepithelial cell attachment. J Med Food, 12(2), 259-70. DOI: 10.1089/jmf.2008.0196
Rafsanjany, N., Senker, J., Brandt, S., Dobrindt, U., & Hensel, A. (2015). In Vivo Consumption of Cranberry Exerts ex Vivo Antiadhesive Activity against FimH-Dominated Uropathogenic Escherichia coli: A Combined in Vivo, ex Vivo, and in Vitro Study of an Extract from Vaccinium macrocarpon. J Agric Food Chem, 63(40), 8804-18. DOI: 10.1021/acs.jafc.5b03030
Rane, H.S., Bernardo, S.M., Howell, A.B., Lee, S.A. (2014). Cranberry-derived proanthocyanidins prevent formation of Candida albicans biofilms in artificial urine through biofilm- and adherence-specific mechanisms. J Antimicrob Chemother, 69(2), 428-36. DOI: 10.1093/jac/dkt398
Rodríguez-Pérez, C., Quirantes-Piné, R., Uberos, J., Jiménez-Sánchez, C., Peña, A., & Segura-Carretero, A. (2016). Antibacterial activity of isolated phenolic compounds from cranberry (Vaccinium macrocarpon) against Escherichia coli. Food & function, 7(3), 1564-1573. DOI:10.1039/c5fo01441g
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Sobota, A.E. (1984). Inhibition of bacterial adherence by cranberry juice: potential use for the treatment of urinary tract infections.J Urol, 131(5), 1013-6. Abstract
Skrovankova, S., Sumczynski, D., Mlcek, J., Jurikova, T., & Sochor, J. (2015). Bioactive compounds and antioxidant activity in different types of berries. International journal of molecular sciences, 16 (10), 24673-24706. doi: 10.3390/ijms161024673
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Sun, J., Marais, J.P.J., Khoo, C., LaPlante, K., Vejborg, R.M., Givskov, M., Tolker-Nielsen, T.,Seeram, N.P., Rowley, D.C. (2015). Cranberry (Vaccinium macrocarpon) oligosaccharides decrease biofilm formation by uropathogenic Escherichia coli. J. Funct. Foods, 17, 235–242. https://doi.org/10.1016/j.jff.2015.05.016
Tao, Y., Pinzon-Arango, P.A., Howel, A.B., & Camesano, T.A. (2011). Oral consumption of cranberry juice cocktail inhibits molecular-scale adhesion of clinical uropathogenic Escherichia coli.J Med Food, 14(7-8), 739-45. DOI: 10.1089/jmf.2010.0154
Tempera, G., Corsello, S., Genovese, C., Caruso, F.E., & Nicolosi, D. (2010). Inhibitory activity of cranberry extract on the bacterial adhesiveness in the urine of women: an ex-vivo study. Int J Immunopathol Pharmacol, 23(2), 611-8. DOI: 10.1177/039463201002300223
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Vasileiou, I., Katsargyris, A., Theocharis, S., & Giaginis, C. (2013). Current clinical status on the preventive effects of cranberry consumption against urinary tract infections. Nutr Res, 33(8), 595-607. DOI: 10.1016/j.nutres.2013.05.018
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Wing, D.A., Rumney, P.J., Preslicka, C.W., & Chung, J.H. (2008). Daily cranberry juice for the prevention of asymptomatic bacteriuria in pregnancy: A randomized, controlled pilot study. J Urol, 180,1367–72. DOI: 10.1016/j.juro.2008.06.016
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Pomegranate: Antimicrobial Effect
Al-Zoreky, N. S. (2009). Antimicrobial activity of pomegranate (Punica granatum L.) fruit peels. International journal of food microbiology, 134(3), 244-248. https://doi.org/10.1016/j.ijfoodmicro.2009.07.002
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Braga, L. C., Shupp, J. W., Cummings, C., Jett, M., Takahashi, J. A., Carmo, L. S., ... & Nascimento, A. M. A. (2005). Pomegranate extract inhibits Staphylococcus aureus growth and subsequent enterotoxin production. Journal of Ethnopharmacology, 96(1), 335-339. https://doi.org/10.1016/j.jep.2004.08.034
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Duman, A. D., Ozgen, M., Dayisoylu, K. S., Erbil, N., & Durgac, C. (2009). Antimicrobial activity of six pomegranate (Punica granatum L.) varieties and their relation to some of their pomological and phytonutrient characteristics. Molecules, 14(5), 1808-1817. DOI: 10.3390/molecules14051808
Hmid, I., Elothmani, D., Hanine, H., Oukabli, A., & Mehinagic, E. (2017). Comparative study of phenolic compounds and their antioxidant attributes of eighteen pomegranate (Punica granatum L.) cultivars grown in Morocco. Arabian Journal of Chemistry, 10, S2675-S2684. https://doi.org/10.1016/j.arabjc.2013.10.011
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Nascimento, G. G., Locatelli, J., Freitas, P. C., & Silva, G. L. (2000). Antibacterial activity of plant extracts and phytochemicals on antibiotic-resistant bacteria. Brazilian journal of microbiology, 31(4), 247-256. Abstract
Naz, S., Siddiqi, R., Ahmad, S., Rasool, S. A., & Sayeed, S. A. (2007). Antibacterial activity directed isolation of compounds from Punica granatum. Journal of food science, 72(9). http://onlinelibrary.wiley.com/doi/10.1111/j.1750-3841.2007.00533.x/abstract
Negi, P. S., & Jayaprakasha, G. K. (2003). Antioxidant and antibacterial activities of Punica granatum peel extracts. Journal of food science, 68(4), 1473-1477. http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2621.2003.tb09669.x/full
Pagliarulo, C., De Vito, V., Picariello, G., Colicchio, R., Pastore, G., Salvatore, P., & Volpe, M. G. (2016). Inhibitory effect of pomegranate (Punica granatum L.) polyphenol extracts on the bacterial growth and survival of clinical isolates of pathogenic Staphylococcus aureus and Escherichia coli. Food chemistry, 190, 824-831. DOI: 10.1016/j.foodchem.2015.06.028
Parseh, H., Hassanpour, S., Emam-Djome, Z., Lavasani, A. S., Mahmoodabady, H. Z., CHabok, M., ... & Ghahsareh, A. M. (2012, April). Antimicrobial properties of Pomegranate (Punica granatum L.) as a Tannin rich Fruit: a review. In The 1st International and The 4th National Congress on Recycling of Organic Waste in Agriculture. Iran .
Rahimi, H. R., Arastoo, M., & Ostad, S. N. (2012). A comprehensive review of Punica granatum (pomegranate) properties in toxicological, pharmacological, cellular and molecular biology researches. Iranian journal of pharmaceutical research: IJPR, 11(2), 385. Article
Reddy, M. K., Gupta, S. K., Jacob, M. R., Khan, S. I., & Ferreira, D. (2007). Antioxidant, antimalarial and antimicrobial activities of tannin-rich fractions, ellagitannins and phenolic acids from Punica granatum L. Planta medica, 53(05), 461-467. DOI: 10.1055/s-2007-967167
Shaygannia, E., Bahmani, M., Zamanzad, B., & Rafieian-Kopaei, M. (2016). A review study on Punica granatum L. Journal of evidence-based complementary & alternative medicine , 21(3), 221-227. DOI: 10.1177/2156587215598039
Voravuthikunchai, S. P., Sririrak, T., Limsuwan, S., Supawita, T., Iida, T., & Honda, T. (2005). Inhibitory effects of active compounds from Punica granatum pericarp on verocytotoxin production by enterohemorrhagic Escherichia coli O157: H7. Journal of health science, 51 (5), 590-596. DOI: 10.1016/j.foodchem.2015.06.028
Wafa, B. A., Makni, M., Ammar, S., Khannous, L., Hassana, A. B., Bouaziz, M., ... & Gdoura, R. (2017). Antimicrobial effect of the Tunisian Nana variety Punica granatum L. extracts against Salmonella enterica (serovars Kentucky and Enteritidis) isolated from chicken meat and phenolic composition of its peel extract. International journal of food microbiology, 241, 123-131. DOI: 10.1016/j.ijfoodmicro.2016.10.007
Probiotics and Supernatant: UTI Support and Management
de Llano, D. G., Arroyo, A., Cárdenas, N., Rodríguez, J. M., Moreno-Arribas, M., & Bartolomé, B. (2017). Strain-specific inhibition of the adherence of uropathogenic bacteria to bladder cells by probiotic Lactobacillus spp. Pathogens and Disease, 75(4). DOI: 10.1093/femspd/ftx043
Ditu, L.M., Chifiriuc, M.C., Bezirtzoglou, E., Marutescu, L., Bleotu, C., Pelinescu, D., Mihaescu, G., Lazar, V. (2014). Immunomodulatory effect of non-viable components of probiotic culture stimulated with heat-inactivated Escherichia coli and Bacillus cereus on holoxenic mice.Microb Ecol Health Dis, 25. DOI: 10.3402/mehd.v25.23239
Fontana, L., Bermudez-Brito, M., Plaza-Diaz, J., Munoz-Quezada, S., & Gil, A. (2013). Sources, isolation, characterisation and evaluation of probiotics. British journal of nutrition, 109(S2), S35-S50. DOI: 10.1017/S0007114512004011
He, X., Zeng, Q., Puthiyakunnon, S., Zeng, Z., Yang, W., Qiu, J… Cao H.. .(2017). Lactobacillus rhamnosus GG [ATCC 53103] supernatant enhance neonatal resistance to systemic Escherichia coli K1 infection by accelerating development of intestinal defense. Sci Rep, 7, 43305. DOI: 10.1038/srep43305
Hütt, P., Shchepetova, J., Loivukene, K., Kullisaar, T., & Mikelsaar, M. (2006). Antagonistic activity of probiotic lactobacilli and bifidobacteria against entero‐and uropathogens. Journal of Applied Microbiology, 100(6), 1324-1332. DOI: 10.1111/j.1365-2672.2006.02857.x
Lazar, V., Miyazaki, Y., Hanawa, T., Chifiriuc, M. C., Ditu, L. M., Marutescu, L., ... & Kamiya, S. (2009). The influence of some probiotic supernatants on the growth and virulence features expression of several selected enteroaggregative E. coli clinical strains.Roum Arch Microbiol Immunol, 68(4), 207-214. Abstract
Lee, S. J., Cha, J., & Lee, J. W. (2016). Probiotics prophylaxis in pyelonephritis infants with normal urinary tracts. World Journal of Pediatrics, 12(4), 425-429. DOI: 10.1007/s12519-016-0013-2
Liévin-Le Moal, V., & Servin, A. L. (2014). Anti-infective activities of lactobacillus strains in the human intestinal microbiota: from probiotics to gastrointestinal anti-infectious biotherapeutic agents. Clinical microbiology reviews, 27(2), 167-199. DOI: 10.1128/CMR.00080-13
Manzoor, A., Ul-Haq, I., Baig, S., Qazi, J. I., & Seratlic, S. (2016). Efficacy of locally isolated lactic acid bacteria against antibiotic-resistant uropathogens.Jundishapur journal of microbiology, 9(1). DOI: 10.5812/jjm.18952
Maurya, P., Mogra, R., & Bajpai, P. (2014). Probiotics: an approach towards health and disease. Trends in Biosciences, 7(20), 3107-3113. Abstract
Shim, Y. H., Lee, S. J., & Lee, J. W. (2016). Antimicrobial activity of lactobacillus strains against uropathogens.Pediatrics International, 58(10), 1009-1013. DOI: 10.1111/ped.12949
Syngai, G. G., Gopi, R., Bharali, R., Dey, S., Lakshmanan, G. A., & Ahmed, G. (2016). Probiotics-the versatile functional food ingredients. Journal of food science and technology, 53(2), 921-933. DOI: 10.1007/s13197-015-2011-0
D-mannose: UTI Support and Management
Domenici, L., Monti, M., Bracchi, C., Giorgini, M., Colagiovanni, V., Muzii, L., & Panici, P. B. (2016). D-mannose: a promising support for acute urinary tract infections in women. A pilot study.Eur Rev Med Pharmacol Sci, 20(13), 2920-5. Article
Kranjčec, B., Papeš, D., Altarac, S.(2014). D-mannose powder for prophylaxis of recurrent urinary tract infections in women: a randomized clinical trial. World J Urol, 32(1), 79-84.DOI: 10.1007/s00345-013-1091-6
Palleschi, G., Carbone, A., Zanello, P. P., Mele, R., Leto, A., Fuschi, A., ... & Maurizi, A. (2017). Prospective study to compare antibiosis versus the association of N-acetylcysteine, D-mannose and Morinda citrifolia fruit extract in preventing urinary tract infections in patients submitted to urodynamic investigation. Archivio Italiano di Urologia e Andrologia, 89(1), 45-50. DOI: 10.4081/aiua.2017.1.45
Panicker, J., Phé, V., Pakzad, M., Haslam, C., Gonzales, G., Curtis, C., ... & Chataway, J. (2016). D-MANNOSE TO PREVENT URINARY TRACT INFECTIONS IN MULTIPLE SCLEROSIS. http://dx.doi.org/10.1136/jnnp-2016-315106.151
Spaulding, C. N., Klein, R. D., Ruer, S., Kau, A. L., Schreiber, H. L., Cusumano, Z. T., ... & Remaut, H. (2017). Selective depletion of uropathogenic E. coli from the gut by a FimH antagonist. Nature, 546(7659), 528-532. DOI: 10.1038/nature22972
Spaulding, C. N., Kau, A. L., Klein, R. D., Janetka, J. W., Gordon, J. I., & Hultgren, S. J. (2017a). Small-molecule inhibitors against type 1 pili selectively target uropathogenic E. coli in the gut and bladder. The FASEB Journal, 31(1 Supplement), 939-9. Abstract
Vicariotto, F. (2014). Effectiveness of an association of a cranberry dry extract, D-mannose, and the two microorganisms Lactobacillus plantarum LP01 and Lactobacillus paracasei LPC09 in women affected by cystitis: a pilot study. Journal of clinical gastroenterology, 48, S96-S101. DOI: 10.1097/MCG.0000000000000224
Cranberries and Helicobacter Pylori
Burger, O., Weiss, E., Sharon, N., Tabak, M., Neeman, I., Ofek, I. (2002). Inhibition of Helicobacter pylori adhesion to human gastric mucus by a high-molecular-weight constituent of cranberry juice. Crit Rev Food Sci Nutr, 42(3), 279-84. DOI: 10.1080/10408390209351916
Burger, O., Ofek, I., Tabak, M., Weiss. E.I,, Sharon, N., & Neeman, I. (2000). A high molecular mass constituent of cranberry juice inhibitsHelicobacter pylori adhesion to human gastric mucus.FEMS Immunol Med Microbiol, 29, 295–301. Abstract
Matsushima, M., Suzuki, T., Masui, A., (Edss). (2008). Growth inhibitory action of cranberry on Helicobacter pylori. J Gastroenterol Hepatol, 2, S175–80. DOI: 10.1111/j.1440-1746.2008.05409.x
Shmuely, H., Yahav, J., Samra, Z., Chodick, G., Koren, R., Niv, Y., Ofek, I. (2007). Effect of cranberry juice on eradication of Helicobacter pylori in patients treated with antibiotics and a proton pump inhibitor.Mol Nutr Food Res, 51(6), 746-51. DOI: 10.1002/mnfr.200600281
Shmuely, H., Burger, O., Neeman, I., Yahav, J., Samra, Z., Niv, Y…. Ofek, I. (2004). Susceptibility of Helicobacter pylori isolates to the antiadhesion activity of a high-molecular-weight constituent of cranberry. Diagn Microbiol Infect Dis, 50(4), 231-5. DOI: 10.1016/j.diagmicrobio.2004.08.011
Zhang, L., Ma, J., Pan, K., Go, V.L., Chen, J., You, W.C. (2005). Efficacy of cranberry juice on Helicobacter pylori infection: A double-blind randomized placebo-controlled trial. Helicobacter, 10, 139–45. DOI: 10.1111/j.1523-5378.2005.00301.x
Cranberries and Pomegranate for Cancer Support
Adams, L.S., Seeram, N.P., Aggarwal, B.B., Takada, Y., Sand, D., Heber, D. (2006). Pomegranate juice, total pomegranate tannins and punicalagin suppress inflammatory cell signaling in colon cancer cells.J Agric Food Chem, 54, 980–5. DOI: 10.1021/jf052005r
Afaq, F., Saleem, M., Krueger, C.G., Reed, J.D., Mukhtar, H. (2005). Anthocyanin- and hydrolysable tannin-rich pomegranate fruit extract modulates MAPK and NF-κBpathways and inhibits skin tumorigenesis in CD-1 mice. Int J Cancer, 113, 423–33. DOI: 10.1002/ijc.20587
Bishayee, A., Mandal, A., Bhattacharyya, P., Bhatia, D. (2016). Pomegranate exerts chemoprevention of experimentally induced mammary tumorigenesis by suppression of cell proliferation and induction of apoptosis. Nutr Cancer, 68(1), 120-30. DOI: 10.1080/01635581.2016.1115094
Castonguay, A., Gali, H., Perchellet, E., Gao, X, Boukharta, M., Jalbert, G…. Perchellet, J. (1997). Antitumorigenic and antipromoting activities of ellagic acid, ellagitannins and oligomeric anthocyanin and procyanidin. Int J Oncol, 10, 367–73. Abstract
Faria, A., & Calhau, C. (2011). The bioactivity of pomegranate: impact on health and disease. Criti Rev Food Sci Nutri, 51(7), 626-34. DOI: 10.1080/10408391003748100
Ferguson, P.J., Kurowska, E.M., Freeman, D.J., Chambers, A.F., Koropatnick, D.J. (2006). In vivo inhibition of growth of human tumor lines by flavonoid fractions from cranberry extract. Nutr Cancer, 56, 86–94. DOI: 10.1207/s15327914nc5601_12
Ferguson, P., Kurowska, E., Freeman, D.J., Chambers, A.F., Koropatnick, D.J. (2004). A flavonoid fraction from cranberry extract inhibits proliferation of human tumor cell lines. J Nutr, 134, 1529–35. Abstract
Griffin, L., Rego, S., Correiro, E., Neto, C., Hart, P. (2005). Induction of Apoptosis in Tumor Cell Lines by Polyphenolic Compounds Isolatedfrom Vaccinium Macrocarpon. Molecular Biology of the Cell, 11, 184a. Citation
Heber, D. (2011). Pomegranate Ellagitannins. In I.F.F., Benzie, & S. Wachtel-Galor (Eds.), Herbal medicine: Biomolecular and clinical aspects. 2nd edition. Boca Raton, FL: CRC Press/Taylor & Francis. Chapter 10
Hochman, N., Houri-Haddad, Y., Koblinski, J., Wahl, L., Roniger, M., Bar-Sinai, A. …Hochman, J. (2008). Cranberry juice constituents impair lymphoma growth andaugment the generation of antilymphoma antibodies in syngeneic mice. Nutr Cancer, 60, 511–7. DOI: 10.1080/01635580801956493
Kandil, F.E., Smith, M. A. L., Rogers, R.B., Pepin, MF., Song, L.L., Pezzuto, J.M., Seigler, D.S. (2002). Composition of a chemopreventive proantho-cyanidin-rich fraction from cranberry fruits responsible for the inhibition of TPA-induced ODC activity. J Agric Food Chem, 50, 1063–9. DOI:10.1021/jf011136z
Kresty, L.A., Weh, K.M., Zeyzus-Johns, B., Perez, L.N., Howell, A.B. (2015). Cranberry proanthocyanidins inhibit esophageal adenocarcinoma in vitro and in vivo through pleiotropic cell death induction and PI3K/AKT/mTOR inactivation. Oncotarget, 6, 33438–33455. DOI: 10.18632/oncotarget.5586
Kresty, L.A., Clarke, J., Ezell, K., Exum, A., Howell, A.B., Guettouche, T. (2011). MicroRNA alterations in Barrett's esophagus, esophageal adenocarcinoma, and esophageal adenocarcinoma cell lines following cranberry extract treatment: Insights for chemoprevention. J. Carcinog, 10, 34. DOI: 10.4103/1477-3163.91110
Kresty, L.A., Howell, A.B., & Baird, M. (2008). Cranberry proanthocyanidins induce apoptosis and inhibit acid-induced proliferation of human esophageal adenocarcinoma cells. J Agric Food Chem, 56 (3), 676-80. DOI: 10.1021/jf071997t
Lansky, E.P., Newman, R.A. (2007). Punica granatum (pomegranate) and its potential for prevention and treatment of inflammation and cancer. J Ethnopharmacol, 109(2), 177-206. DOI: 10.1016/j.jep.2006.09.006
Liberty, A.M., Amoroso, J.W., Hart, P.E., Neto, C.C. (2009). Cranberry PACs and triterpenoids: anti-cancer activities in colon tumor cell lines. Proceedings of the Second International Symposium on Human Health Effects of Fruits and Vegetables. Acta Horticulturae, 841, 61–66. DOI: 10.17660/ActaHortic.2009.841.4
Liu, M.L., Lin, L.Q., Song, B.B., Wang, L.F., Zhang, C.P., & Liu J.R. (2009). Cranberry phytochemical extract inhibits SGC-7901 cell growth and human tumor xenografts in Balb/c nu/nu mice. J Agric Food Chem, 57, 762–8. DOI: 10.1021/jf802780k
Longtin R. (2003). The pomegranate: Nature's power fruit? J Natl Cancer Inst, 95, 346–8. DOI: https://doi.org/10.1093/jnci/95.5.346
Neto, C.C. (2007). Cranberry and its phytochemicals: a review of in vitro anticancer studies. J Nutr, 137(1), 186S-193S. Article
Neto, C.C., Krueger, C.G., Lamoureaux, T.L., Kondo, M, Vaisberg, A.J., Hurta, R.A.R. … Reed, J.D. (2006). MALDI-TOF MS characterization of proanthocyanidins from cranberry fruit (Vaccinium macrocarpon) that inhibit tumor cell growth and matrix metalloproteinase expression in vitro. J Sci Food Agric, 86, 18–25. DOI:10.1002/jsfa.2347
Panth, N., Manandhar, B., Paudel, K.R. (2017). Anticancer Activity of Punica granatum (Pomegranate): A Review. Phytother Res, 31(4), 568-578. DOI:10.1002/ptr.5784
Pinzon-Arango, P.A., Liu, Y., Camesano, T.A. (2009). Role of cranberry on bacterial adhesion forces and implications for Escherichia coli-uroepithelial cell attachment. J Med Food, 12, 259–70. DOI: 10.1089/jmf.2008.0196
Prasain, J.K., Rajbhandari, R., Keeton, A.B., Piazza, G.A., Barnes, S. (2016). Metabolism and growth inhibitory activity of cranberry derived flavonoids in bladder cancer cells. Food Funct, 7(9), 4012-4019. DOI:10.1039/c6fo00499g
Seeram, N.P. (2008). Berry fruits for cancer prevention: current status and future prospects. J Agric Food Chem; 56(3): 630-5. DOI: 10.1021/jf072504n
Seeram, N.P., Adams, L.S., Hardy, M.L., Heber, D. (2004). Total cranberry extract versus its phytochemical constituents: Antiproliferative and synergistic effects against human tumor cell lines.J Agric Food Chem, 52, 2512–7. DOI: 10.1021/jf0352778
Seeram, N.P., Adams, L.S., Henning, S.M., Niu, Y., Zhang, Y., Nair, M.G., Heber, D. (2005). In vitro anti-proliferative, apoptotic and antioxidant activities of punicalagin, ellagic acid and a total pomegranate tannin extract are enhanced in combination with other polyphenols as found in pomegranate juice. J Nutr Biochem, 16, 360–7. DOI: 10.1016/j.jnutbio.2005.01.006
Sharma, P., McClees, S.F., Afaq, F. (2017). Pomegranate for Prevention and Treatment of Cancer: An Update. Molecules, 22(1). DOI: 10.3390/molecules22010177
Sun, J., & Liu, R.H. (2006). Cranberry phytochemical extracts induce cell cycle arrest and apoptosis in human MCF-7 breast cancer cells. Cancer Lett, 241, 124–34. DOI: 10.1016/j.canlet.2005.10.027
Taheri Rouhi, S.Z., Sarker, M.M., Rahmat, A., Alkahtani, S.A., Othman, F. (2017). The effect of pomegranate fresh juice versus pomegranate seed powder on metabolic indices, lipid profile, inflammatory biomarkers, and the histopathology of pancreatic islets of Langerhans in streptozotocin-nicotinamide induced type 2 diabetic Sprague-Dawley rats. BMC Complement Altern Med, 17(1):156. DOI: 10.1186/s12906-017-1667-6
Tibullo, D., Caporarello, N., Giallongo, C., Anfuso, C.D., Genovese, C., Arlotta, C… Raccuia, S.A. (2016). Antiproliferative and Antiangiogenic Effects of Punica granatum Juice (PGJ) in Multiple Myeloma (MM).Nutrients, 8(10). DOI: 10.3390/nu8100611
Vattem, D. A., JANG, H. D., Levin, R., & Shetty, K. (2006). Synergism of cranberry phenolics with ellagic acid and rosmarinic acid for antimutagenic and DNA protection functions. Journal of food biochemistry, 30(1), 98-116. Abstract
Vu, K.D., Carlettini, H., Bouvet, J., Cote, J., Doyon, G., Sylvain, J.-F., Lacroix, M. (2012). Effect of different cranberry extracts and juices during cranberry juice processing on the antiproliferative activity against two colon cancer cell lines. Food Chem., 132, 959–967. https://doi.org/10.1016/j.foodchem.2011.11.078
Weh, K.M., Clarke, J., & Kresty, L.A. (2016). Cranberries and Cancer: An Update of Preclinical Studies Evaluating the Cancer Inhibitory Potential of Cranberry and Cranberry Derived Constituents.Antioxidants (Basel), 5(3). DOI: 10.3390/antiox5030027
Weh, K.M., Aiyer, H.S., Howell, A.B., Kresty, L.A. (2016). Cranberry proanthocyanidins modulate reactive oxygen species in Barrett's and esophageal adenocarcinoma cell lines. J Berry Res, 6(2), 125-136. DOI:10.3233/JBR-160122
Yan, X., Murphy, B.T., Hammond, G.B., Vinson, J.A., Neto, C.C. (2002). Antioxidant activities and antitumor screening of extracts from cranberry fruit (Vaccinium macrocarpon). J. Agric. Food Chem, 50, 5844–5849. DOI:10.1021/jf0202234
Pomegranate and Cranberries: Prostate Cancer Support
Bonetta, A., & Di Pierro, F. (2012). Enteric-coated, highly standardized cranberry extract reduces risk of UTIs and urinary symptoms during radiotherapy for prostate carcinoma. Cancer Manag Res, 4 , 281-6. DOI: 10.2147/CMAR.S35342
Deziel, B., MacPhee, J., Patel, K. Catalli, A., Kulka, M., Neto, C., … Hurta, R. (2012). American cranberry (Vaccinium macrocarpon) extract affects human prostate cancer cell growth via cell cycle arrest by modulating expression of cell cycle regulators. Food Funct, 3(5), 556-64. DOI:10.1039/c2fo10145a
Hong, M.Y., Seeram, N.P., & Heber, D. (2008). Pomegranate polyphenols down-regulate expression of androgen-synthesizing genes in human prostate cancer cells overexpressing the androgen receptor. J Nutr Biochem, 19(12), 848-55. DOI: 10.1016/j.jnutbio.2007.11.006
Koyama, S., Cobb, L.J., Mehta, H.H., Seeram, N.P., Heber, D., Pantuck, A.J., & Cohen, P. (2010). Pomegranate extract induces apoptosis in human prostate cancer cells by modulation of the IGF-IGFBP axis. Growth Horm IGF Res, 20(1), 55-62. DOI: 10.1016/j.ghir.2009.09.003
Malik, A., Afaq, F., Sarfaraz, S., Adhami, V.M., Syed, D.N., Mukhtar, H. (2005). Pomegranate fruit juice for chemoprevention and chemotherapy of prostate cancer. Proc Natl Acad Sci USA, 102, 14813–8. DOI: 10.1073/pnas.0505870102
Pantuck, A.J., Leppert, J.T., Zomorodian, N., Aronson, W., Hong, J., Barnard, R.J., … Belldegrun, A. (2006). Phase II study of pomegranate juice for men with rising prostate-specific antigen following surgery or radiation for prostate cancer. Clin Cancer Res, 12(13), 4018-26. DOI: 10.1158/1078-0432.CCR-05-2290
Retting, M.B., Heber, D., An, J. Seeram, N.P., Rao, J.Y., Rao, J.Y., Liu, H., … Pantuck, A. (2008). Pomegranate extract inhibits androgen-independent prostate cancer growth through a nuclear factor-kappaB-dependent mechanism. Mol Cancer ther, 7(9), 2662-71. DOI: 10.1158/1535-7163.MCT-08-0136
Seeram, N.P., Aronson, W.J., Zhang, Y., Henning, S.M., Moro, A., Lee, R.P., … Heber, D. (2007). Pomegranate ellagitannin-derived metabolites inhibit prostate cancer growth and localize to the mouse prostate gland.J Agric Food Chem, 55(19), 7732-7. DOI: 10.1021/jf071303g
Seeram, N.P., Henning, S.M., Zhang, Y., Suchard, M., Li, Z., & Heber, D. (2006). Pomegranate juice ellagitannin metabolites are present in human plasma and some persist in urine for up to 48 hours.J Agric Food Chem, 136(10), 2481-5. Article
Seeram, N.P., Adams, L.S., Hardy, M.L., & Heber, D. (2004). Total cranberry extract versus its phytochemical constituents: antiproliferative and synergistic effects against human tumor cell lines.J Agric Food Chem, 52(9), 2512-7. DOI: 10.1021/jf0352778
Cranberries & Pomegranate: Heart Health, Gut Microbiota, Liver Support
Aviram, M., Volkova, N., Coleman, R., Dreher, M., Reddy, M.K., Ferreira D., Rosenblat, M. (2008). Pomegranate phenolics from the peels, arils, and flowers are antiatherogenic: studies in vivo in atherosclerotic apolipoprotein e-deficient (E 0) mice and in vitro in cultured macrophages and lipoproteins. J Agric Food Chem, 56(3),1148-57. DOI: 10.1021/jf071811q
Aviram, M., Dornfeld, L., Kaplan, M., Coleman, R., Gaitini, D., Nitecki, S…. Fuhrman, B. (2002). Pomegranate juice flavonoids inhibit low-density lipoprotein oxidation and cardiovascular diseases: studies in atherosclerotic mice and in humans. Drugs Exp Clin Res, 28(2-3), 49-62. Abstract
Aviram, M., Dornfeld, L., Rosenblat, M., Volkova, N., Kaplan, M., Coleman, R., Hayek, T., Presser, D., & Fuhrman, B. (2000). Pomegranate juice consumption reduces oxidative stress, atherogenic modifications to LDL, and platelet aggregation: Studies in humans and in atherosclerotic apolipoprotein E-deficient mice. Am J Clin Nutr,71, 1062–1076. Article
Blumberg, J.B., Basu, A., Krueger, C.G., Lila, M.A., Neto, C.C., Novotny, JA… Toner, C.D. (2016). Impact of Cranberries on Gut Microbiota and Cardiometabolic Health: Proceedings of the Cranberry Health Research Conference 2015. Adv Nutr, 7(4), 759S-70S. DOI: 10.3945/an.116.012583
Bishayee, A., Thoppil, R.J., Darvesh, A.S., Ohanyan, V., Meszaros, J.G., Bhatia, D. (2013). Pomegranate phytoconstituents blunt the inflammatory cascade in a chemically induced rodent model of hepatocellular carcinogenesis. J. Nutr. Biochem, 24, 178–187. DOI: 10.1016/j.jnutbio.2012.04.009
Bishayee, A., Bhatia, D., Thoppil, R.J., Darvesh, A.S., Nevo, E. & Lansky, E.P. (2011). Pomegranate-mediated chemoprevention of experimental hepatocarcinogenesis involves Nrf2-regulated antioxidant mechanisms.Carcinogenesis, 32(6), 688-96. DOI: 10.1093/carcin/bgr045
Chu, Y.F., & Liu, R.H. (2005). Cranberries inhibit LDL oxidation and induce LDL receptor expression in hepatocytes. Life Sci, 77, 1892–1901. DOI: 10.1016/j.lfs.2005.04.002
Gil, M.I., Tomàs-Barberàn, F.A., Hess-Pierce, B., Holcroft, D.M., Kader, A.A. (2000). Antioxidant activity of pomegranate juice and its relationship with phenolic composition and processing. J Agric Food Chem, 48, 4581–9. Abstract
Kaplan, M., Hayek, T., Raz, A., Coleman, R., Dornfeld, L., Vaya, J., & Aviram, M. (2001). Pomegranate juice supplementation to atherosclerotic mice reduces macrophage lipid peroxidation, cellular cholesterol accumulation and development of atherosclerosis.The Journal of nutrition, 131(8), 2082-2089. Abstract
Novotny, J. A., Baer, D. J., Khoo, C., Gebauer, S. K., & Charron, C. S. (2015). Cranberry juice consumption lowers markers of cardiometabolic risk, including blood pressure and circulating C-reactive protein, triglyceride, and glucose concentrations in adults. The Journal of nutrition,145(6), 1185-1193. DOI: 10.3945/jn.114.203190
McKay, D. L., & Blumberg, J. B. (2007). Cranberries (Vaccinium macrocarpon) and cardiovascular disease risk factors. Nutrition reviews, 65(11), 490-502. https://doi.org/10.1111/j.1753-4887.2007.tb00273.x
Taheri Rouhi, S.Z., Sarker, M.M., Rahmat, A., Alkahtani, S.A., Othman, F. (2017). The effect of pomegranate fresh juice versus pomegranate seed powder on metabolic indices, lipid profile, inflammatory biomarkers, and the histopathology of pancreatic islets of Langerhans in streptozotocin-nicotinamide induced type 2 diabetic Sprague-Dawley rats. BMC Complement Altern Med, 17(1):156. DOI: 10.1186/s12906-017-1667-6
Vinson, J.A., Bose, P., Proch, J. AI Kharrant, H., & Samman, N. (2008). Cranberries and cranberry products: powerful in vitro, ex vivo, and in vivo sources of antioxidants. J Agric Food Chem, 56(14), 5884-91. DOI: 10.1021/jf073309b
Duthie, S. J., Jenkinson, A. M., Crozier, A., Mullen, W., Pirie, L., Kyle, J., ... & Duthie, G. G. (2006). The effects of cranberry juice consumption on antioxidant status and biomarkers relating to heart disease and cancer in healthy human volunteers. European journal of nutrition, 45(2), 113-122. DOI: 10.1007/s00394-005-0572-9
Pomegranate: Neuro-regeneration and Cognitive Support
Braidy, N., Essa, M. M., Poljak, A., Selvaraju, S., Al-Adawi, S., Manivasagm, T., ... & Guillemin, G. J. (2016). Consumption of pomegranates improves synaptic function in a transgenic mice model of Alzheimer's disease. Oncotarget, 7(40), 64589. DOI: 10.18632/oncotarget.10905
Braidy, N., Selvaraju, S., Essa, M.M., Vishnav, R., Al-Adawi, S., Al-Senawi, H., … Guillemin, G.J. (2013). Neuroprotective effects of a variety of pomegranate juice extracts against MPTP-induced cytotoxicity and oxidative stress in human primary neurons. Oxid Med Cell Longev. DOI:10.1155/2013/685909
Essa, M.M., Subash, S., Akbar, M., Al-Adawi, S., & Guillemin, G.J. (2015). Long-term dietary supplementation of pomegranates, figs and dates alleviate neuroinflammation in a transgenic mouse model of Alzheimer's disease. PLoS One, 10(3). DOI: 10.1371/journal.pone.0120964
Subash, S., Braidy, N., Essa, M.M., Al-Buraiki, Z., Vaishnav, R., Al-Adawi, S., Al-Asmi, A., Guillemin, G.J. (2014). Long Term (15 Months) Dietary Supplementation with Pomegranates from Oman Attenuates Cognitive and Behavioural Deficts in a Transgenic Mice Model of Alzheimer's Disease. Nutrition, 31223-9.DOI: 10.1016/j.nut.2014.06.004
Yan, T., Ma, H., Liu, W., Niesen, D.B., Shah, N., Crews, R., … Seeram, N.P. (2016). Pomegranate's Neuroprotective Effects against Alzheimer's Disease Are Mediated by Urolithins, Its Ellagitannin-Gut Microbial Derived Metabolites. ACS Chem Neurosci, 7(1), 26-33. DOI: 10.1021/acschemneuro.5b00260
The Bioavailability of Cranberry and Pomegranate
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Grace, M.H., Massey, A.R., Mbeunkui. F., Yousef, G.G., & Lila, M.A. (2012). Comparison of health-relevant flavonoids in commonly consumed cranberry products. J Food Sci, 77(8), H176-83. DOI: 10.1111/j.1750-3841.2012.02788.x
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Ohnishi R, Ito H, Kasajima N, editors. (2006). Urinary excretion of anthocyanins in humans after cranberry juice ingestion.Biosci Biotechnol Biochem, 70, 1681–7. DOI: 10.1271/bbb.60023
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Cranberry Pomegranate Synbiotic: UTI Support
A Proprietary blend of: 500mg
Phytonutrients- Organic Cranberry 6%, Pomegranate Extract with 40% Punicalagins, D-Mannose.
BioImmersion Probiotic Master Blend – Probiotics- Bifidobacterium longum, Lactobacillus casei, Lactobacillus acidophilus, Lactobacillus bulgaricus and streptococcus thermophilus; Prebiotic- Inulin from chicory Root; Supernatant- probiotic metabolites, and ORNs. 30 billion CFU.
Capsule- Cellulose & Water
CRANBERRY POMEGRANATE — The Cranberry Pomegranate is designed to care for the bladder, kidneys, and prostate. *
UTI (urinary tract infection) support: Take 2-4 capsules every 3 hours till the bladder relaxes and urine flow improves, then reduce to 2 caps X 3 daily for several days. For maintenance, take 1-2 a day. Add Garlic as an antimicrobial agent, 1-2 capsules, and Original for added probiotics and fiber.*
Prostate support: Take 1-2 a day. If it is difficult to urinate, take 2-4 every 3 hours till inflammation subsides and urine flows. Add 1 capsule of Phyto Power, Fructo Borate, and 1 teaspoon of No 7 to reduce swelling, and along with 1 capsule of Glucosamine & Sulforaphanes (broccoli cruciferous sprouts) to support DNA cellular integrity.*
Bloating and swelling: Excellent to help the kidneys and bladder flush. Take 2 capsules with extra water till swelling or bloating subsides (every 3 hours).*
Our favorite: The Cran/Pom is Dr. Dohrea Bardell’s third favorite product (yes, she has a list: Blueberry Extract and No 7, respectively). During travel or stressful times, the microbiome (GI Tract), along with the bladder and prostate, can easily become unbalanced (bloating, swelling, aching). The Cranberry Pomegranate is an exceptionally potent anti-inflammatory for the whole GI Tract, bladder, prostate, and even helps that achy low back pain. Take up to 4-6 when very uncomfortable, and drink plenty of water. *
Description
Urinary tract infection (UTI) is one of the most common bacterial infections (Foxman, 2014), often caused by Gram-negative bacteria, enterobacteriaceae (Bader, Loeb & Brooks, 2017), and more specifically within this large bacterial family, the familiar Escherichia coli (Jensen et al., 2017). In recent years, more women suffer from chronic UTIs due to the climbing rise of antibiotic resistant bacteria. As a natural alternative or a supportive adjunct treatment with antibiotics, the Cranberry Pomegranate Synbiotic Formula offers well-researched phyto nutrients, probiotics, prebiotics, and D- mannose. Studies and clinical trials find cranberries (Bader et al., 2017; Jensen et al., 2017; de Llano et al., 2015), Pomegranates (Pagliarulo et al., 2016; Heber, 2011; Duman et al., 2009), along with probiotics, prebiotics, and D- mannose (Spaulding et al., 2017; 2017a; Domenici et al., 2016), to offer effective management and support for UTI.*
Historically, cranberries and cranberry juice have long been used to alleviate urinary tract infections, with research linking the ability of cranberries’ proanthocyanidins (Krueger et al., 2013) to inhibit adhesion of E. coli bacteria (Neto, 2007). As early as 1933, research by Fellers et al. has shown cranberries to positively effect urinary health. Cowan’s (1999) seminal work on plant products as antimicrobial agents, which includes cranberries, has been cited in approximately 7,500 research articles. Studies on cranberries show not only an alternative to antibiotic but also as a daily supplement for a steady prevention of UTIs.*
Recent studies continue to observe and explain cranberries’ excellent antimicrobial properties, especially the phenol elements and mechanism that are beneficial for the management and prevention of UTI (Jensen et al., 2017; Rodríguez-Pérez et al., 2017; Baranowska & Bartoszek, 2016; Sagdic et al, 2006; Lee, 2000). As stated above, proanthocyanidins in cranberries are found to prevent the adherence of Escherichia coli to uroepithelial cells in the urinary tract (Sun et al., 2015; Rowley, 2012; Burger et al., 2000), and disrupt hard to treat biofilm-mediated infections caused by Pseudomonas aeruginosa (Ulrey et al., 2014).*
Cranberries also pack other antimicrobial, antioxidant and anti-inflammatory benefits. With their powerful anti-adhesion properties, cranberries are found to inhibit growth of Helicobacter Pylori (Shmuely et al., 2007; Zhang et al., 2005; Burger et al., 2002), suppress tumor cell proliferation and offer support during cancer treatment (Bshayee et al., 2016; Kresty et al., 2015), as well as lower markers of cardio-metabolic risk (Novotny et al., 2015), and enhance the GI’s microbiota (Blumberg et al., 2016). Cranberries are shown to be effective agents for health.*
Pomegranate has enjoyed an exalted status since ancient times, and no wonder (Parseh et al., 2012). Studies show pomegranates contain 124 different phyto-nutrients with curative and preventative qualities. The pomegranate fruit is actually considered a berry, or more accurately, each pomegranate contains 600 seeds, each surrounded by fleshy white to dark red pulp (Rahimi et al., 2012).*
With their potent polyphenolic flavonoids, pomegranates show higher concentrations of antioxidants than green tea (Noda et al., 2002; Nori-Okamoto et al., 2004), cranberries, apples, grapes, or pears (Hmid et al., 2017; Heber, 2011; Heber et al., 2006). The pomegranate’s high concentration of polyphenols wields an inhibitory effect on pathogenic Staphylococcus aureus and Escherichia coli, serving as natural antimicrobial agents (Pagliarulo et al., 2016; Naz et al., 2007; Voravuthikunchai et al., 2005). Other microbial organisms are shown to be sensitive to the pomegranate phenolic flavonoids. Nascimento et al. (2000) tested extracts from a variety of plants in search of a natural support against antibiotic resistant microorganisms and found the pomegranate to be especially effective against Pseudomonas aeruginosa. Machado et al. (2002) identified antimicrobial ellagitannin of the pomegranate to be valuable to treat methicillin-resistant Staphylococcus aureus (MRSA) strains.*
Similarly, the pomegranate’s antioxidants work as scavengers and metal chelators (Kulkarni et al., 2007). The antioxidant, antimalarial, and antimicrobial activities of the tannin-rich fractions, ellagitannins and phenolic acids from pomegranates offer excellent daily dietary food supplement to enhance the immune system (Reddy et al., 2007).*
Probiotics and Supernatant are important to the health of our urogenital system. The genus Lactobacillus has been studied for their promising preventative and/or treatment potential against UTIs (de Llano et al., 2017). Three strains of lactobacillus were tested for their capabilities to inhibit pathogenic adherence of E. coli, E. faecalis, and Staphylococcus epidermidis to T24 epithelial bladder cells. L. salivarious, L. acidophilus showed a significantly inhibited the adherence of pathogens (de Llano et al., 2017; see also Shim et al., 2016). Lactobacillus species were also studies with infants experiencing acute pyelonephritis [kidney infection], and found effective in the prevention of urinary tract infections (Lee et al., 2016).*
The “anti-infective activities” of lactobacillus strains are exhibiting a great promise as innovative anti-infectious agents (Liévin-Le Moal et al., 2014), and especially for recurrent UTIs (Manzoor et al., 2016).*
Depletion of vaginal Lactobacilli has also found in research to be linked with UTI risk, which suggests that repletion (re-colonization of Lactobacilli) might be beneficial (Syngai et al., 2016; Fontana et al., 2013; Maurya et al., 2014).*
Supernatant is the fermented medium crated during the culturing process of probiotics. Supernatant is the fermented “soup” that contains important probiotic metabolites which is comprised of enzymes, peptides, proteins, vitamins, and other nutrients and factors, including antimicrobials such as bacitracins. Supernatant is shown in research to have powerful antimicrobial properties with the potential to block adhesion, invasion and translocation of E. coli, yet it is gentle enough to be used to ‘enhance neonatal resistance to systemic Escherichia coli K1 infection by accelerating development of intestinal defense’ (He et al., 2017). In fact, Lazar et al. (2009) in vitro study concluded that the soluble probiotic metabolites, or supernatant, might actually interfere with the beginning stages of adherence and colonization of selected E. coli. This means that the supernatant itself exudes protective effects (Lazar et al., 2009), as well as work synergistically with probiotics organism to stimulate the immune system against pathogenic invasion (Ditu et al., 2014).*
D-mannose has long shown an ability to support acute UTIs, inhibiting bacterial adhesion to the urothelium (Domenici et al., 2016; Kranjčec et al., 2014). Testing more sensitive populations, such as people with multiple sclerosis (MS) who suffer from recurrent UTIs, showed that D-mannose effected a reduction in the number of UTIs as well as reduction for the need of antibiotics (Panicker et al., 2016).*
Since 150 million people suffer from UTIs annually, using natural foods and nutriceutical agents to combat recurrence of UTI infections is advisable (Spaulding et al., 2017). The use of cranberries, pomegranates, probiotics, supernatant, and D-mannose form a potent synergistic effect that is shown in research to be very effective (Vicarotto, 2014).*
There are many more health functions that cranberries and pomegranates perform. For many years cranberries and pomegranates were studied to understand their anti-tumorigenic elements (e.g., Castonguay et al., 1997). More recent studies continue to reveal and explain the bioactivity of pomegranate (Panth et al., 2017; Bishayee et al., 2016; Faria & Calhau, 2011) and cranberries (Kresty et al., 2015; Hochman et al., 2008; Ferguson et al., 2006) as promising suppressants and inhibitors of different kinds of cancer cells (Weh et al., 2016; Liberty et al., 2009; Adams et al., 2006).*
And there is more: Research studies find pomegranate and cranberries phenolics to contribute to heart health (Taheri et al., 2017; Novotny et al., 2015; Aviram et al., 2008, 2002), to balance the gut microbiota (Blumberg et al., 2016), and to offer liver support (Bishayee et al., 2013, 2011). Check the Research Tab for more in depth studies.*
The Cranberry Pomegranate Synbiotic Formula is an excellent choice for UTIs. Cranberries, Pomegranates, Probiotics, supernatant, and D-mannose have all shown in research to provide a potent effect against UTIs. The combination of these ingredients offers a promising natural supplement to prevent and maintain a healthy balance of the urogenital system. We suggest 2-4 capsules twice daily for UTI management, and 1-2 capsules daily for preventative support.*
REFERENCES
Bader, M. S., Loeb, M., & Brooks, A. A. (2017). An update on the management of urinary tract infections in the era of antimicrobial resistance. Postgraduate medicine, 129(2), 242-258. http://dx.doi.org/10.1080/00325481.2017.1246055
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Research
FOOD SCIENCE: THE APPLICATION AND USE OF CRANBERRY, POMEGRANATE, PROBIOTICS (BULGARIAN ORIGIN), SUPERNATANT, D-MANNOSE, AND CHICORY SOLUBLE FIBER.*
Historical and Clinical Reviews of Cranberries and Pomegranate
Heber, D. (2011). Pomegranate Ellagitannins. In I.F.F., Benzie, & S. Wachtel-Galor (Eds.), Herbal medicine: Biomolecular and clinical aspects. 2nd edition. Boca Raton, FL: CRC Press/Taylor & Francis. https://www.ncbi.nlm.nih.gov/books/NBK92772/
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Cranberries : UTI Support and Management
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Cowan, M. M. (1999). Plant products as antimicrobial agents.Clinical microbiology reviews, 12(4), 564-582. Abstract
Davidson, E., Zimmermann, B.F., Jungfer, E., & Chrubasik-Hausmann, S. (2014). Prevention of Urinary Tract Infections with Vaccinium Products. Phytotherapy Research, 28, (3), 465-470. DOI: 10.1002/ptr.5047
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Jensen, H.D., Carsten, S., Christensen, S.B., & Krogfelt, K.A. (2017). Cranberry juice and combinations of its organic acids are effective against experimental urinary tract infection. Front Microbiol, 8, 542. doi: 10.3389/fmicb.2017.00542
Kaspar, K.L., Howell, A.B., & Khoo, C. (2015). A randomized, double-blind, placebo-controlled trial to assess the bacterial anti-adhesion effects of cranberry extract beverages.Food Funct, 6(4), 1212-7. DOI: 10.1039/c4fo01018c
Krueger, C. G., Reed, J. D., Feliciano, R. P., & Howell, A. B. (2013). Quantifying and characterizing proanthocyanidins in cranberries in relation to urinary tract health. Analytical and bioanalytical chemistry, 405(13), 4385-4395. DOI: 10.1007/s00216-013-6750-3
Liu, Y., Pinzón-Arango, P.A., Gallardo-Moreno, A.M., Camesano, T.A. (2010). Direct adhesion force measurements between E. coli and human uroepithelial cells in cranberry juice cocktail. Mol Nutr Food Res, 54(12), 1744-52. DOI: 10.1002/mnfr.200900535
Liu, Y., Gallardo-Moreno, A.M., Pinzon-Arango, P.A., Reynolds, Y., Rodriguez, G., Camesano TA. (2008). Cranberry changes the physicochemical surface properties of E. coli and adhesion with uroepithelial cells. Colloids Surf B Biointerfaces, 65(1), 35-42. DOI: 10.1016/j.colsurfb.2008.02.012
Liu, Y., Black, M.A., Caron, L., Camesano, T.A. (2006). Role of cranberry juice on molecular-scale surface characteristics and adhesion behavior of Escherichia coli. Biotechnol Bioeng, 93(2), 297-305. DOI: 10.1002/bit.20675
Margetis, D., Roux, D., Gaudry, S., Messika, J., Bouvet, O., Branger, C….Ricard, J.D. (2015). Effects of Proanthocyanidins on Adhesion, Growth, and Virulence of Highly Virulent Extraintestinal Pathogenic Escherichia coli Argue for Its Use to Treat Oropharyngeal Colonization and Prevent Ventilator-Associated Pneumonia. Crit Care Med, 43(6), e170-8. DOI: 10.1097/CCM.0000000000000972
Mathers, M.J., von Rundstedt, F., Brandt, A.S., Koig, M., Lazica, D.A., & Roth, S. (2009). [Myth or truth. Cranberry juice for prophylaxis and treatment of recurrent urinary tract infection]. Urologe A, 48 (10), 1203-9. [Article in German]. DOI: 10.1007/s00120-009-2051-z
Mathison, B.D., Kimble, L.L., Kaspar, K.L., Khoo, C., Chew, B.P. (2014). Consumption of cranberry beverage improved endogenous antioxidant status and protected against bacteria adhesion in healthy humans: a randomized controlled trial. Nutr Res, 34(5), 420-7. DOI: http://dx.doi.org/10.1016/j.nutres.2014.03.006
McMurdo, M.E., Argo, I., Phillips, G., Daly, F., & Davey, P. (2009). Cranberry or trimethoprim for the prevention of recurrent urinary tract infections? A randomized controlled trial in older women.J Antimicrob Chemother, 63, 389–95. DOI: 10.1093/jac/dkn489
McMurdo, M.E., Bissett, L.Y., Price, R.J., Phillips, G., & Crombie, I.K. (2005). Does ingestion of cranberry juice reduce symptomatic urinary tract infections in older people in hospital? A double-blind, placebo-controlled trial. Age Ageing, 34(3), 256-61. DOI: 10.1093/ageing/afi101
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Pérez-López, F.R., Haya, J., Chedraui, P. (2009). Vaccinium macrocarpon: an interesting option for women with recurrent urinary tract infections and other health benefits. J Obstet Gynaecol Res, 35(4), 630-9. DOI: 10.1111/j.1447-0756.2009.01026.x
Pinzón-Arango, P.A., Liu, Y., Camesano, T.A. (2009). Role of cranberry on bacterial adhesion forces and implications for Escherichia coli-uroepithelial cell attachment. J Med Food, 12(2), 259-70. DOI: 10.1089/jmf.2008.0196
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Sun, J., Marais, J.P.J., Khoo, C., LaPlante, K., Vejborg, R.M., Givskov, M., Tolker-Nielsen, T.,Seeram, N.P., Rowley, D.C. (2015). Cranberry (Vaccinium macrocarpon) oligosaccharides decrease biofilm formation by uropathogenic Escherichia coli. J. Funct. Foods, 17, 235–242. https://doi.org/10.1016/j.jff.2015.05.016
Tao, Y., Pinzon-Arango, P.A., Howel, A.B., & Camesano, T.A. (2011). Oral consumption of cranberry juice cocktail inhibits molecular-scale adhesion of clinical uropathogenic Escherichia coli.J Med Food, 14(7-8), 739-45. DOI: 10.1089/jmf.2010.0154
Tempera, G., Corsello, S., Genovese, C., Caruso, F.E., & Nicolosi, D. (2010). Inhibitory activity of cranberry extract on the bacterial adhesiveness in the urine of women: an ex-vivo study. Int J Immunopathol Pharmacol, 23(2), 611-8. DOI: 10.1177/039463201002300223
Ulrey, R.K., Barksdale, S.M., Zhou, W., van Hoek, M.L. (2014). Cranberry proanthocyanidins have anti-biofilm properties against Pseudomonas aeruginosa. BMC Complement Altern Med, 14, 499. DOI: 10.1186/1472-6882-14-499
Vasileiou, I., Katsargyris, A., Theocharis, S., & Giaginis, C. (2013). Current clinical status on the preventive effects of cranberry consumption against urinary tract infections. Nutr Res, 33(8), 595-607. DOI: 10.1016/j.nutres.2013.05.018
Wang, C. H., Fang, C. C., Chen, N. C., Liu, S. S., Yu, P. H … Chen, S.C. (2012). Cranberry-containing products for prevention of urinary tract infections in susceptible populations: a systematic review and meta-analysis of randomized controlled trials. Arch. Intern. Med, 172, 988–996. DOI: 10.1001/archinternmed.2012.3004
Wing, D.A., Rumney, P.J., Preslicka, C.W., & Chung, J.H. (2008). Daily cranberry juice for the prevention of asymptomatic bacteriuria in pregnancy: A randomized, controlled pilot study. J Urol, 180,1367–72. DOI: 10.1016/j.juro.2008.06.016
Zafriri, D., Ofek, I., Pocino, A.R., & Sharon, N. (1989). Inhibitory activity of cranberry juice on adherence of type 1 and type P-fimbriated Escherichia coli to eucaryotic cells. Antimicrob Agents Chemother, 33, 92–8. Abstract
Pomegranate: Antimicrobial Effect
Al-Zoreky, N. S. (2009). Antimicrobial activity of pomegranate (Punica granatum L.) fruit peels. International journal of food microbiology, 134(3), 244-248. https://doi.org/10.1016/j.ijfoodmicro.2009.07.002
Bialonska D, Kasimsetty SG, Schrader KK, Ferreira D. (2009). The effect of pomegranate (Punica granatum L.) byproducts and ellagitannins on the growth of human gut bacteria. J Agric Food Chem, 57(18):8344-9. DOI:10.1021/jf901931b
Braga, L. C., Shupp, J. W., Cummings, C., Jett, M., Takahashi, J. A., Carmo, L. S., ... & Nascimento, A. M. A. (2005). Pomegranate extract inhibits Staphylococcus aureus growth and subsequent enterotoxin production. Journal of Ethnopharmacology, 96(1), 335-339. https://doi.org/10.1016/j.jep.2004.08.034
Cowan, M. M. (1999). Plant products as antimicrobial agents.Clinical microbiology reviews, 12(4), 564-582. Article
Dahham, S. S., Ali, M. N., Tabassum, H., & Khan, M. (2010). Studies on antibacterial and antifungal activity of pomegranate (Punica granatum L.). Am. Eurasian J. Agric. Environ. Sci, 9(3), 273-281. Abstract
Duman, A. D., Ozgen, M., Dayisoylu, K. S., Erbil, N., & Durgac, C. (2009). Antimicrobial activity of six pomegranate (Punica granatum L.) varieties and their relation to some of their pomological and phytonutrient characteristics. Molecules, 14(5), 1808-1817. DOI: 10.3390/molecules14051808
Hmid, I., Elothmani, D., Hanine, H., Oukabli, A., & Mehinagic, E. (2017). Comparative study of phenolic compounds and their antioxidant attributes of eighteen pomegranate (Punica granatum L.) cultivars grown in Morocco. Arabian Journal of Chemistry, 10, S2675-S2684. https://doi.org/10.1016/j.arabjc.2013.10.011
Jurenka, J. (2008). Therapeutic applications of pomegranate (Punica granatum L.): a review. Alternative medicine review, 13 (2), 128. Article
Machado, T. D. B., Leal, I. C., Amaral, A. C. F., Santos, K., Silva, M. G. D., & Kuster, R. M. (2002). Antimicrobial ellagitannin of Punica granatum fruits. Journal of the Brazilian Chemical Society, 13(5), 606-610. Article
Nascimento, G. G., Locatelli, J., Freitas, P. C., & Silva, G. L. (2000). Antibacterial activity of plant extracts and phytochemicals on antibiotic-resistant bacteria. Brazilian journal of microbiology, 31(4), 247-256. Abstract
Naz, S., Siddiqi, R., Ahmad, S., Rasool, S. A., & Sayeed, S. A. (2007). Antibacterial activity directed isolation of compounds from Punica granatum. Journal of food science, 72(9). http://onlinelibrary.wiley.com/doi/10.1111/j.1750-3841.2007.00533.x/abstract
Negi, P. S., & Jayaprakasha, G. K. (2003). Antioxidant and antibacterial activities of Punica granatum peel extracts. Journal of food science, 68(4), 1473-1477. http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2621.2003.tb09669.x/full
Pagliarulo, C., De Vito, V., Picariello, G., Colicchio, R., Pastore, G., Salvatore, P., & Volpe, M. G. (2016). Inhibitory effect of pomegranate (Punica granatum L.) polyphenol extracts on the bacterial growth and survival of clinical isolates of pathogenic Staphylococcus aureus and Escherichia coli. Food chemistry, 190, 824-831. DOI: 10.1016/j.foodchem.2015.06.028
Parseh, H., Hassanpour, S., Emam-Djome, Z., Lavasani, A. S., Mahmoodabady, H. Z., CHabok, M., ... & Ghahsareh, A. M. (2012, April). Antimicrobial properties of Pomegranate (Punica granatum L.) as a Tannin rich Fruit: a review. In The 1st International and The 4th National Congress on Recycling of Organic Waste in Agriculture. Iran .
Rahimi, H. R., Arastoo, M., & Ostad, S. N. (2012). A comprehensive review of Punica granatum (pomegranate) properties in toxicological, pharmacological, cellular and molecular biology researches. Iranian journal of pharmaceutical research: IJPR, 11(2), 385. Article
Reddy, M. K., Gupta, S. K., Jacob, M. R., Khan, S. I., & Ferreira, D. (2007). Antioxidant, antimalarial and antimicrobial activities of tannin-rich fractions, ellagitannins and phenolic acids from Punica granatum L. Planta medica, 53(05), 461-467. DOI: 10.1055/s-2007-967167
Shaygannia, E., Bahmani, M., Zamanzad, B., & Rafieian-Kopaei, M. (2016). A review study on Punica granatum L. Journal of evidence-based complementary & alternative medicine , 21(3), 221-227. DOI: 10.1177/2156587215598039
Voravuthikunchai, S. P., Sririrak, T., Limsuwan, S., Supawita, T., Iida, T., & Honda, T. (2005). Inhibitory effects of active compounds from Punica granatum pericarp on verocytotoxin production by enterohemorrhagic Escherichia coli O157: H7. Journal of health science, 51 (5), 590-596. DOI: 10.1016/j.foodchem.2015.06.028
Wafa, B. A., Makni, M., Ammar, S., Khannous, L., Hassana, A. B., Bouaziz, M., ... & Gdoura, R. (2017). Antimicrobial effect of the Tunisian Nana variety Punica granatum L. extracts against Salmonella enterica (serovars Kentucky and Enteritidis) isolated from chicken meat and phenolic composition of its peel extract. International journal of food microbiology, 241, 123-131. DOI: 10.1016/j.ijfoodmicro.2016.10.007
Probiotics and Supernatant: UTI Support and Management
de Llano, D. G., Arroyo, A., Cárdenas, N., Rodríguez, J. M., Moreno-Arribas, M., & Bartolomé, B. (2017). Strain-specific inhibition of the adherence of uropathogenic bacteria to bladder cells by probiotic Lactobacillus spp. Pathogens and Disease, 75(4). DOI: 10.1093/femspd/ftx043
Ditu, L.M., Chifiriuc, M.C., Bezirtzoglou, E., Marutescu, L., Bleotu, C., Pelinescu, D., Mihaescu, G., Lazar, V. (2014). Immunomodulatory effect of non-viable components of probiotic culture stimulated with heat-inactivated Escherichia coli and Bacillus cereus on holoxenic mice.Microb Ecol Health Dis, 25. DOI: 10.3402/mehd.v25.23239
Fontana, L., Bermudez-Brito, M., Plaza-Diaz, J., Munoz-Quezada, S., & Gil, A. (2013). Sources, isolation, characterisation and evaluation of probiotics. British journal of nutrition, 109(S2), S35-S50. DOI: 10.1017/S0007114512004011
He, X., Zeng, Q., Puthiyakunnon, S., Zeng, Z., Yang, W., Qiu, J… Cao H.. .(2017). Lactobacillus rhamnosus GG [ATCC 53103] supernatant enhance neonatal resistance to systemic Escherichia coli K1 infection by accelerating development of intestinal defense. Sci Rep, 7, 43305. DOI: 10.1038/srep43305
Hütt, P., Shchepetova, J., Loivukene, K., Kullisaar, T., & Mikelsaar, M. (2006). Antagonistic activity of probiotic lactobacilli and bifidobacteria against entero‐and uropathogens. Journal of Applied Microbiology, 100(6), 1324-1332. DOI: 10.1111/j.1365-2672.2006.02857.x
Lazar, V., Miyazaki, Y., Hanawa, T., Chifiriuc, M. C., Ditu, L. M., Marutescu, L., ... & Kamiya, S. (2009). The influence of some probiotic supernatants on the growth and virulence features expression of several selected enteroaggregative E. coli clinical strains.Roum Arch Microbiol Immunol, 68(4), 207-214. Abstract
Lee, S. J., Cha, J., & Lee, J. W. (2016). Probiotics prophylaxis in pyelonephritis infants with normal urinary tracts. World Journal of Pediatrics, 12(4), 425-429. DOI: 10.1007/s12519-016-0013-2
Liévin-Le Moal, V., & Servin, A. L. (2014). Anti-infective activities of lactobacillus strains in the human intestinal microbiota: from probiotics to gastrointestinal anti-infectious biotherapeutic agents. Clinical microbiology reviews, 27(2), 167-199. DOI: 10.1128/CMR.00080-13
Manzoor, A., Ul-Haq, I., Baig, S., Qazi, J. I., & Seratlic, S. (2016). Efficacy of locally isolated lactic acid bacteria against antibiotic-resistant uropathogens.Jundishapur journal of microbiology, 9(1). DOI: 10.5812/jjm.18952
Maurya, P., Mogra, R., & Bajpai, P. (2014). Probiotics: an approach towards health and disease. Trends in Biosciences, 7(20), 3107-3113. Abstract
Shim, Y. H., Lee, S. J., & Lee, J. W. (2016). Antimicrobial activity of lactobacillus strains against uropathogens.Pediatrics International, 58(10), 1009-1013. DOI: 10.1111/ped.12949
Syngai, G. G., Gopi, R., Bharali, R., Dey, S., Lakshmanan, G. A., & Ahmed, G. (2016). Probiotics-the versatile functional food ingredients. Journal of food science and technology, 53(2), 921-933. DOI: 10.1007/s13197-015-2011-0
D-mannose: UTI Support and Management
Domenici, L., Monti, M., Bracchi, C., Giorgini, M., Colagiovanni, V., Muzii, L., & Panici, P. B. (2016). D-mannose: a promising support for acute urinary tract infections in women. A pilot study.Eur Rev Med Pharmacol Sci, 20(13), 2920-5. Article
Kranjčec, B., Papeš, D., Altarac, S.(2014). D-mannose powder for prophylaxis of recurrent urinary tract infections in women: a randomized clinical trial. World J Urol, 32(1), 79-84.DOI: 10.1007/s00345-013-1091-6
Palleschi, G., Carbone, A., Zanello, P. P., Mele, R., Leto, A., Fuschi, A., ... & Maurizi, A. (2017). Prospective study to compare antibiosis versus the association of N-acetylcysteine, D-mannose and Morinda citrifolia fruit extract in preventing urinary tract infections in patients submitted to urodynamic investigation. Archivio Italiano di Urologia e Andrologia, 89(1), 45-50. DOI: 10.4081/aiua.2017.1.45
Panicker, J., Phé, V., Pakzad, M., Haslam, C., Gonzales, G., Curtis, C., ... & Chataway, J. (2016). D-MANNOSE TO PREVENT URINARY TRACT INFECTIONS IN MULTIPLE SCLEROSIS. http://dx.doi.org/10.1136/jnnp-2016-315106.151
Spaulding, C. N., Klein, R. D., Ruer, S., Kau, A. L., Schreiber, H. L., Cusumano, Z. T., ... & Remaut, H. (2017). Selective depletion of uropathogenic E. coli from the gut by a FimH antagonist. Nature, 546(7659), 528-532. DOI: 10.1038/nature22972
Spaulding, C. N., Kau, A. L., Klein, R. D., Janetka, J. W., Gordon, J. I., & Hultgren, S. J. (2017a). Small-molecule inhibitors against type 1 pili selectively target uropathogenic E. coli in the gut and bladder. The FASEB Journal, 31(1 Supplement), 939-9. Abstract
Vicariotto, F. (2014). Effectiveness of an association of a cranberry dry extract, D-mannose, and the two microorganisms Lactobacillus plantarum LP01 and Lactobacillus paracasei LPC09 in women affected by cystitis: a pilot study. Journal of clinical gastroenterology, 48, S96-S101. DOI: 10.1097/MCG.0000000000000224
Cranberries and Helicobacter Pylori
Burger, O., Weiss, E., Sharon, N., Tabak, M., Neeman, I., Ofek, I. (2002). Inhibition of Helicobacter pylori adhesion to human gastric mucus by a high-molecular-weight constituent of cranberry juice. Crit Rev Food Sci Nutr, 42(3), 279-84. DOI: 10.1080/10408390209351916
Burger, O., Ofek, I., Tabak, M., Weiss. E.I,, Sharon, N., & Neeman, I. (2000). A high molecular mass constituent of cranberry juice inhibitsHelicobacter pylori adhesion to human gastric mucus.FEMS Immunol Med Microbiol, 29, 295–301. Abstract
Matsushima, M., Suzuki, T., Masui, A., (Edss). (2008). Growth inhibitory action of cranberry on Helicobacter pylori. J Gastroenterol Hepatol, 2, S175–80. DOI: 10.1111/j.1440-1746.2008.05409.x
Shmuely, H., Yahav, J., Samra, Z., Chodick, G., Koren, R., Niv, Y., Ofek, I. (2007). Effect of cranberry juice on eradication of Helicobacter pylori in patients treated with antibiotics and a proton pump inhibitor.Mol Nutr Food Res, 51(6), 746-51. DOI: 10.1002/mnfr.200600281
Shmuely, H., Burger, O., Neeman, I., Yahav, J., Samra, Z., Niv, Y…. Ofek, I. (2004). Susceptibility of Helicobacter pylori isolates to the antiadhesion activity of a high-molecular-weight constituent of cranberry. Diagn Microbiol Infect Dis, 50(4), 231-5. DOI: 10.1016/j.diagmicrobio.2004.08.011
Zhang, L., Ma, J., Pan, K., Go, V.L., Chen, J., You, W.C. (2005). Efficacy of cranberry juice on Helicobacter pylori infection: A double-blind randomized placebo-controlled trial. Helicobacter, 10, 139–45. DOI: 10.1111/j.1523-5378.2005.00301.x
Cranberries and Pomegranate for Cancer Support
Adams, L.S., Seeram, N.P., Aggarwal, B.B., Takada, Y., Sand, D., Heber, D. (2006). Pomegranate juice, total pomegranate tannins and punicalagin suppress inflammatory cell signaling in colon cancer cells.J Agric Food Chem, 54, 980–5. DOI: 10.1021/jf052005r
Afaq, F., Saleem, M., Krueger, C.G., Reed, J.D., Mukhtar, H. (2005). Anthocyanin- and hydrolysable tannin-rich pomegranate fruit extract modulates MAPK and NF-κBpathways and inhibits skin tumorigenesis in CD-1 mice. Int J Cancer, 113, 423–33. DOI: 10.1002/ijc.20587
Bishayee, A., Mandal, A., Bhattacharyya, P., Bhatia, D. (2016). Pomegranate exerts chemoprevention of experimentally induced mammary tumorigenesis by suppression of cell proliferation and induction of apoptosis. Nutr Cancer, 68(1), 120-30. DOI: 10.1080/01635581.2016.1115094
Castonguay, A., Gali, H., Perchellet, E., Gao, X, Boukharta, M., Jalbert, G…. Perchellet, J. (1997). Antitumorigenic and antipromoting activities of ellagic acid, ellagitannins and oligomeric anthocyanin and procyanidin. Int J Oncol, 10, 367–73. Abstract
Faria, A., & Calhau, C. (2011). The bioactivity of pomegranate: impact on health and disease. Criti Rev Food Sci Nutri, 51(7), 626-34. DOI: 10.1080/10408391003748100
Ferguson, P.J., Kurowska, E.M., Freeman, D.J., Chambers, A.F., Koropatnick, D.J. (2006). In vivo inhibition of growth of human tumor lines by flavonoid fractions from cranberry extract. Nutr Cancer, 56, 86–94. DOI: 10.1207/s15327914nc5601_12
Ferguson, P., Kurowska, E., Freeman, D.J., Chambers, A.F., Koropatnick, D.J. (2004). A flavonoid fraction from cranberry extract inhibits proliferation of human tumor cell lines. J Nutr, 134, 1529–35. Abstract
Griffin, L., Rego, S., Correiro, E., Neto, C., Hart, P. (2005). Induction of Apoptosis in Tumor Cell Lines by Polyphenolic Compounds Isolatedfrom Vaccinium Macrocarpon. Molecular Biology of the Cell, 11, 184a. Citation
Heber, D. (2011). Pomegranate Ellagitannins. In I.F.F., Benzie, & S. Wachtel-Galor (Eds.), Herbal medicine: Biomolecular and clinical aspects. 2nd edition. Boca Raton, FL: CRC Press/Taylor & Francis. Chapter 10
Hochman, N., Houri-Haddad, Y., Koblinski, J., Wahl, L., Roniger, M., Bar-Sinai, A. …Hochman, J. (2008). Cranberry juice constituents impair lymphoma growth andaugment the generation of antilymphoma antibodies in syngeneic mice. Nutr Cancer, 60, 511–7. DOI: 10.1080/01635580801956493
Kandil, F.E., Smith, M. A. L., Rogers, R.B., Pepin, MF., Song, L.L., Pezzuto, J.M., Seigler, D.S. (2002). Composition of a chemopreventive proantho-cyanidin-rich fraction from cranberry fruits responsible for the inhibition of TPA-induced ODC activity. J Agric Food Chem, 50, 1063–9. DOI:10.1021/jf011136z
Kresty, L.A., Weh, K.M., Zeyzus-Johns, B., Perez, L.N., Howell, A.B. (2015). Cranberry proanthocyanidins inhibit esophageal adenocarcinoma in vitro and in vivo through pleiotropic cell death induction and PI3K/AKT/mTOR inactivation. Oncotarget, 6, 33438–33455. DOI: 10.18632/oncotarget.5586
Kresty, L.A., Clarke, J., Ezell, K., Exum, A., Howell, A.B., Guettouche, T. (2011). MicroRNA alterations in Barrett's esophagus, esophageal adenocarcinoma, and esophageal adenocarcinoma cell lines following cranberry extract treatment: Insights for chemoprevention. J. Carcinog, 10, 34. DOI: 10.4103/1477-3163.91110
Kresty, L.A., Howell, A.B., & Baird, M. (2008). Cranberry proanthocyanidins induce apoptosis and inhibit acid-induced proliferation of human esophageal adenocarcinoma cells. J Agric Food Chem, 56 (3), 676-80. DOI: 10.1021/jf071997t
Lansky, E.P., Newman, R.A. (2007). Punica granatum (pomegranate) and its potential for prevention and treatment of inflammation and cancer. J Ethnopharmacol, 109(2), 177-206. DOI: 10.1016/j.jep.2006.09.006
Liberty, A.M., Amoroso, J.W., Hart, P.E., Neto, C.C. (2009). Cranberry PACs and triterpenoids: anti-cancer activities in colon tumor cell lines. Proceedings of the Second International Symposium on Human Health Effects of Fruits and Vegetables. Acta Horticulturae, 841, 61–66. DOI: 10.17660/ActaHortic.2009.841.4
Liu, M.L., Lin, L.Q., Song, B.B., Wang, L.F., Zhang, C.P., & Liu J.R. (2009). Cranberry phytochemical extract inhibits SGC-7901 cell growth and human tumor xenografts in Balb/c nu/nu mice. J Agric Food Chem, 57, 762–8. DOI: 10.1021/jf802780k
Longtin R. (2003). The pomegranate: Nature's power fruit? J Natl Cancer Inst, 95, 346–8. DOI: https://doi.org/10.1093/jnci/95.5.346
Neto, C.C. (2007). Cranberry and its phytochemicals: a review of in vitro anticancer studies. J Nutr, 137(1), 186S-193S. Article
Neto, C.C., Krueger, C.G., Lamoureaux, T.L., Kondo, M, Vaisberg, A.J., Hurta, R.A.R. … Reed, J.D. (2006). MALDI-TOF MS characterization of proanthocyanidins from cranberry fruit (Vaccinium macrocarpon) that inhibit tumor cell growth and matrix metalloproteinase expression in vitro. J Sci Food Agric, 86, 18–25. DOI:10.1002/jsfa.2347
Panth, N., Manandhar, B., Paudel, K.R. (2017). Anticancer Activity of Punica granatum (Pomegranate): A Review. Phytother Res, 31(4), 568-578. DOI:10.1002/ptr.5784
Pinzon-Arango, P.A., Liu, Y., Camesano, T.A. (2009). Role of cranberry on bacterial adhesion forces and implications for Escherichia coli-uroepithelial cell attachment. J Med Food, 12, 259–70. DOI: 10.1089/jmf.2008.0196
Prasain, J.K., Rajbhandari, R., Keeton, A.B., Piazza, G.A., Barnes, S. (2016). Metabolism and growth inhibitory activity of cranberry derived flavonoids in bladder cancer cells. Food Funct, 7(9), 4012-4019. DOI:10.1039/c6fo00499g
Seeram, N.P. (2008). Berry fruits for cancer prevention: current status and future prospects. J Agric Food Chem; 56(3): 630-5. DOI: 10.1021/jf072504n
Seeram, N.P., Adams, L.S., Hardy, M.L., Heber, D. (2004). Total cranberry extract versus its phytochemical constituents: Antiproliferative and synergistic effects against human tumor cell lines.J Agric Food Chem, 52, 2512–7. DOI: 10.1021/jf0352778
Seeram, N.P., Adams, L.S., Henning, S.M., Niu, Y., Zhang, Y., Nair, M.G., Heber, D. (2005). In vitro anti-proliferative, apoptotic and antioxidant activities of punicalagin, ellagic acid and a total pomegranate tannin extract are enhanced in combination with other polyphenols as found in pomegranate juice. J Nutr Biochem, 16, 360–7. DOI: 10.1016/j.jnutbio.2005.01.006
Sharma, P., McClees, S.F., Afaq, F. (2017). Pomegranate for Prevention and Treatment of Cancer: An Update. Molecules, 22(1). DOI: 10.3390/molecules22010177
Sun, J., & Liu, R.H. (2006). Cranberry phytochemical extracts induce cell cycle arrest and apoptosis in human MCF-7 breast cancer cells. Cancer Lett, 241, 124–34. DOI: 10.1016/j.canlet.2005.10.027
Taheri Rouhi, S.Z., Sarker, M.M., Rahmat, A., Alkahtani, S.A., Othman, F. (2017). The effect of pomegranate fresh juice versus pomegranate seed powder on metabolic indices, lipid profile, inflammatory biomarkers, and the histopathology of pancreatic islets of Langerhans in streptozotocin-nicotinamide induced type 2 diabetic Sprague-Dawley rats. BMC Complement Altern Med, 17(1):156. DOI: 10.1186/s12906-017-1667-6
Tibullo, D., Caporarello, N., Giallongo, C., Anfuso, C.D., Genovese, C., Arlotta, C… Raccuia, S.A. (2016). Antiproliferative and Antiangiogenic Effects of Punica granatum Juice (PGJ) in Multiple Myeloma (MM).Nutrients, 8(10). DOI: 10.3390/nu8100611
Vattem, D. A., JANG, H. D., Levin, R., & Shetty, K. (2006). Synergism of cranberry phenolics with ellagic acid and rosmarinic acid for antimutagenic and DNA protection functions. Journal of food biochemistry, 30(1), 98-116. Abstract
Vu, K.D., Carlettini, H., Bouvet, J., Cote, J., Doyon, G., Sylvain, J.-F., Lacroix, M. (2012). Effect of different cranberry extracts and juices during cranberry juice processing on the antiproliferative activity against two colon cancer cell lines. Food Chem., 132, 959–967. https://doi.org/10.1016/j.foodchem.2011.11.078
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Weh, K.M., Aiyer, H.S., Howell, A.B., Kresty, L.A. (2016). Cranberry proanthocyanidins modulate reactive oxygen species in Barrett's and esophageal adenocarcinoma cell lines. J Berry Res, 6(2), 125-136. DOI:10.3233/JBR-160122
Yan, X., Murphy, B.T., Hammond, G.B., Vinson, J.A., Neto, C.C. (2002). Antioxidant activities and antitumor screening of extracts from cranberry fruit (Vaccinium macrocarpon). J. Agric. Food Chem, 50, 5844–5849. DOI:10.1021/jf0202234
Pomegranate and Cranberries: Prostate Cancer Support
Bonetta, A., & Di Pierro, F. (2012). Enteric-coated, highly standardized cranberry extract reduces risk of UTIs and urinary symptoms during radiotherapy for prostate carcinoma. Cancer Manag Res, 4 , 281-6. DOI: 10.2147/CMAR.S35342
Deziel, B., MacPhee, J., Patel, K. Catalli, A., Kulka, M., Neto, C., … Hurta, R. (2012). American cranberry (Vaccinium macrocarpon) extract affects human prostate cancer cell growth via cell cycle arrest by modulating expression of cell cycle regulators. Food Funct, 3(5), 556-64. DOI:10.1039/c2fo10145a
Hong, M.Y., Seeram, N.P., & Heber, D. (2008). Pomegranate polyphenols down-regulate expression of androgen-synthesizing genes in human prostate cancer cells overexpressing the androgen receptor. J Nutr Biochem, 19(12), 848-55. DOI: 10.1016/j.jnutbio.2007.11.006
Koyama, S., Cobb, L.J., Mehta, H.H., Seeram, N.P., Heber, D., Pantuck, A.J., & Cohen, P. (2010). Pomegranate extract induces apoptosis in human prostate cancer cells by modulation of the IGF-IGFBP axis. Growth Horm IGF Res, 20(1), 55-62. DOI: 10.1016/j.ghir.2009.09.003
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Ingredients
Cranberry Pomegranate Synbiotic: UTI Support
A Proprietary blend of: 500mg
Phytonutrients- Organic Cranberry 6%, Pomegranate Extract with 40% Punicalagins, D-Mannose.
BioImmersion Probiotic Master Blend – Probiotics- Bifidobacterium longum, Lactobacillus casei, Lactobacillus acidophilus, Lactobacillus bulgaricus and streptococcus thermophilus; Prebiotic- Inulin from chicory Root; Supernatant- probiotic metabolites, and ORNs. 30 billion CFU.
Capsule- Cellulose & Water
Protocol
CRANBERRY POMEGRANATE — The Cranberry Pomegranate is designed to care for the bladder, kidneys, and prostate. *
UTI (urinary tract infection) support: Take 2-4 capsules every 3 hours till the bladder relaxes and urine flow improves, then reduce to 2 caps X 3 daily for several days. For maintenance, take 1-2 a day. Add Garlic as an antimicrobial agent, 1-2 capsules, and Original for added probiotics and fiber.*
Prostate support: Take 1-2 a day. If it is difficult to urinate, take 2-4 every 3 hours till inflammation subsides and urine flows. Add 1 capsule of Phyto Power, Fructo Borate, and 1 teaspoon of No 7 to reduce swelling, and along with 1 capsule of Glucosamine & Sulforaphanes (broccoli cruciferous sprouts) to support DNA cellular integrity.*
Bloating and swelling: Excellent to help the kidneys and bladder flush. Take 2 capsules with extra water till swelling or bloating subsides (every 3 hours).*
Our favorite: The Cran/Pom is Dr. Dohrea Bardell’s third favorite product (yes, she has a list: Blueberry Extract and No 7, respectively). During travel or stressful times, the microbiome (GI Tract), along with the bladder and prostate, can easily become unbalanced (bloating, swelling, aching). The Cranberry Pomegranate is an exceptionally potent anti-inflammatory for the whole GI Tract, bladder, prostate, and even helps that achy low back pain. Take up to 4-6 when very uncomfortable, and drink plenty of water. *