Revolution Health & Wellness

Rev Reflux

As Seen On

Rev RefluxMany factors impact digestion, the stomach’s mucosal lining, and the overall health of the upper gastrointestinal (GI) tract. For various reasons, there may be temporary upset in the balance of flora present in the gastric environment. A wide range of treatments exist for the approximately 25-40% of Americans who suffer from occasional common upper GI discomforts. Whereas an effort is commonly made to either neutralize or block gastric acid, Rev Reflux, a zinc L-carnosine complex, supports the stomach’s natural “cytoprotective” defense mechanisms without negatively impacting stomach pH. In human studies, including four- and eight-week clinical trials among 691 subjects, zinc L-carnosine exhibited high efficacy without any serious side effects.

Carnosine is a naturally occurring dipeptide composed of the amino acids L-histidine and beta-alanine. Carnosine can form stable complexes (ligands) with ion minerals like zinc and copper. Rev Reflux contains a unique, proprietary zinc L-carnosine complex that has been in wide use in Japan since 1994. Rev Reflux differs chemically and biologically from a simple combination of zinc and L-carnosine and has been shown to be approximately three times more effective than supplementing individually with either zinc sulfate or L-carnosine.

A healthy gastric mucosal lining protects the upper gastrointestinal tract unless it is overburdened by the damaging effects of stress, bacteria, or irritating substances. Since L-carnosine and zinc each have mucosa-supportive properties, it is not surprising that the zinc L-carnosine ligand significantly protects and has been shown to enhance the integrity of the gastric lining. Thus, a healthy balance of flora may be re-established within the stomach in a relatively short time frame. In addition to its support of mucosa integrity, Rev Reflux has been shown, in a study on rats, to enhance cellular resistance to ethanol without affecting endogenous prostaglandins. This is highly relevant because prostaglandins are key components of the mucosa. This zinc L-carnosine complex has also been shown to have anti-urease activity, which may indirectly support the gastric mucosa by maintaining a healthy balance of flora in the stomach.

Zinc L-carnosine complex does not rapidly break down in the stomach because it is a polymer. Japanese researchers found that this prolonged-release complex adheres to areas of the stomach lining and forms a new mixed ligand complex with other body components (perhaps proteins, like albumin) for extra support. At some point, a ligand exchange frees the L-carnosine and zinc from the complex and makes each available to optimize the health of the mucosal lining. In addition to the benefits these nutrients have in the GI tract, L-carnosine has antioxidant activity and zinc participates in the body’s healthy natural response to inflammation. Animal studies have demonstrated that the zinc L-carnosine complex maintains the homeostasis of the gastric mucosa by its antioxidative, membrane-stabilizing capability and by protecting gastric cells via promotion of mucous production. The zinc L-carnosine complex also blunts genetic proinflammatory signaling and the release of proinflammatory cytokine expression in the gastric epithelial cells. A 2012 phase III clinical trial in Japan demonstrated a mechanism of action that explains why, in dietary zinc-deficient rats, zinc L-carnosine administration restored the lingual epithelium’s zinc content. Interestingly, it also improved deficiency-induced delayed cell proliferation of taste bud cells.

Revolution Health & Wellness Clinic Supplements FDA Statement

 

Rev Reflux Supplement Facts; Revolution Supplement

 

SGS Label; Supplement Facts Label

 

Directions:

Swallow with liquid or chew one tablet immediately after breakfast and one tablet before bedtime, or as directed by your healthcare practitioner.

References:

1. Sanduleanu S, Jonkers D, De Bruïne A, et al. Double gastric infection with Helicobacter pylori and non-Helicobacter pylori bacteria during acid-suppressive therapy: increase of pro-inflammatory cytokines and development of atrophic gastritis. Aliment Pharmacol Ther. 2001 Aug;15(8):1163-75. [PMID: 11472319]

2. Compilation of numerous studies presented in Jpn Pharmacol Ther. 1992;(20)1.

3. Korolkiewicz RP, Fujita A, Seto K, et al. Polaprezinc exerts a salutary effect on impaired healing of gastric lesions in diabetic rats. Dig Dis Sci. 2000;45(6):1200-1209. [PMID:10877238]

4. Nishiwaki H, Kato S, Sugamoto S, et al. Ulcerogenic and healing impairing actions of monochloramine in rat stomachs: effects of zinc L-carnosine, polaprezinc. J Physiol Pharmacol 1999;50:183-95. [PMID: 10424716]

5. Arakawa T, Satoh H, Nakamura A, et al. Effects of zinc L-carnosine on gastric mucosal and cell damage caused by ethanol in rats. Correlation with endogenous prostaglandin E2. Dig Dis Sci. 1990;35:559-66. [PMID: 2331952]

6. Matsukura T, Tanaka H. Applicability of zinc complex of L-carnosine for medical use. Biochemistry (Mosc). 2000 Jul;65(7):817-23. [PMID: 10951100]

7. Guiotto A, Calderan A, Ruzza P, et al. Carnosine and carnosine-related antioxidants: a review. Curr Med Chem. 2005;12(20):2293-315. [PMID: 16181134]

8. Sempértegui F, Díaz M, Mejía R, et al. Low concentrations of zinc in gastric mucosa are associated with increased severity of Helicobacter pylori-induced inflammation. Helicobacter. 2007 Feb;12(1):43-8. [PMID: 17241300]

9. Seiki M, Aita H, Ueki S, et al. Effect of Z-103 on wound healing by dermal incision in guinea pigs [in Japanese]. Nippon Yakurigaku Zasshi. 1992 Aug;100(2):165-72. [PMID: 1385281]

10. Shimada T, Watanabe N, Ohtsuka Y, et al. Polaprezinc down-regulates proinflammatory cytokine-induced nuclear factor-kappaB activation and interleukin-8 expression in gastric epithelial cells. J Pharmacol Exp Ther. 1999 Oct;291(1); 345-52. [PMID: 10490923]

11. Takei M. The development of polaprezinc research [in Japanese]. Yakugaku Zasshi. 2012;132(3):271-7. [PMID: 22382829]