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Muscle Sport Liver Pro Revolution™
Muscle Sport Liver Pro Revolution™

Liver Pro Revolution™

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$59.99
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LIVER FUNCTION SUPPORT*

  • May increase the rate of protein synthesis in liver cells and encourage subsequent repair after injury to the cells*
  • Stimulates bile secretion and benefits the liver by helping it to eliminate toxins*
  • Fights against various forms of oxidation.*

Description

The liver is one of the most important, underrated organs in the body. It is responsible for over 500 health functions that are crucial to sustain life, and it is the epicenter of metabolism.

Of these 500, three are of vital importance. First, the liver filters the blood coming from the digestive tract before passing it to the rest of the body, a critical step in filtering out toxins and directing nutrients.

Second, the liver detoxifies chemicals and metabolizes drugs. Third, the liver makes enzymes responsible for proper digestion and intestinal function.

As you can clearly see, the liver helps take care of the body as a whole. But that begs the question... what takes care of the liver?

This is why MuscleSport developed Liver Pro Revolution™. A comprehensive formula that helps support healthy liver function using the following ingredients:

  • Milk Thistle Extract - A liver therapeutic compound that may increase the rate of protein synthesis in liver cells and encourage subsequent repair after injury to the cells. 
  • L-Glutathione - Heavily involved in the detoxification of our body, so it is no surprise that it is found in its highest concentrations in the liver.
  • Tumeric Extract - Turmeric can uniquely assist the enzymes that are responsible for flushing out known toxins.
  • Artichoke Powder - This extract appears to have the ability to stimulate bile secretion and benefits the liver by helping it to eliminate toxins.

Without a doubt, Liver Pro Revolution™ is the premier liver health matrix on the market today. It is formulated to reinforce one of your body's hardest working organs, the liver, by detoxing, purifying, and protecting it.

 

*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Supplement Facts

FAQs

Q: What is the best way to take Liver Pro Revolution?

A: As a dietary supplement, take one serving (1 Capsule) upon waking. For optimal performance, take an additional serving before bed.

 

Q: What physiological functions does the liver serve in the body?

A: The liver plays over 500 roles in the human body but the most important roles are the liver cleans your blood, metabolizes nutrients, produces a digestive liquid called bile, and stores energy in the form of glycogen.

 

Q: What other MuscleSport products do you recommend stacking with Liver Pro Revolution?

A: To promote overall health we recommend stacking Liver Pro Revolution with Adrenal Revolution, Joint Revolution, and Multi Vita Revolution.

References

Milk Thistle Extract

1. Mulrow, C., Lawrence, V., Jacobs, B., Dennehy, C., Sapp, J., Ramirez, G., ... & Chiquette, E. (2000). Milk thistle: effects on liver disease and cirrhosis and clinical adverse effects: summary.

2. Abenavoli, L., Capasso, R., Milic, N., & Capasso, F. (2010). Milk thistle in liver diseases: past, present, future. Phytotherapy Research, 24(10), 1423-1432.

3. Pradhan, S. C., & Girish, C. (2006). A hepatoprotective herbal drug, silymarin from experimental pharmacology to clinical medicine. Indian Journal of Medical Research, 124(5), 491.

N-Acetyl Cysteine

1. Holdiness, M. R. (1991). Clinical pharmacokinetics of N-acetylcysteine. Clinical pharmacokinetics, 20(2), 123-134.

2. Wang, L., Wang, Z., & Liu, J. (2010). Protective effect of N-acetylcysteine on experimental chronic lead nephrotoxicity in immature female rats. Human & experimental toxicology, 29(7), 581-591.

3. Kasperczyk, S., Dobrakowski, M., Kasperczyk, A., Ostałowska, A., & Birkner, E. (2013). The administration of N-acetylcysteine reduces oxidative stress and regulates glutathione metabolism in the blood cells of workers exposed to lead. Clinical Toxicology, 51(6), 480-486.

4. Kasperczyk, A., Słowińska-Łożyńska, L., Dobrakowski, M., Zalejska-Fiolka, J., & Kasperczyk, S. (2014). The effect of lead-induced oxidative stress on blood viscosity and rheological properties of erythrocytes in lead-exposed humans. Clinical hemorheology and microcirculation, 56(3), 187-195.

L-Glutathione

1. Amano J, Suzuki A, Sunamori M. Salutary effect of reduced glutathione on renal function in coronary artery bypass operation. J Am Coll Surg 1994;179:714-20. View abstract.

2. Amores-Sanchez MI, Medina MA. Glutamine, as a precursor of glutathione, and oxidative stress. Mol Genet Metab 1999;67:100-5. View abstract.

3. Anderson ME. Glutathione: an overview of biosynthesis and modulation. Chem Biol Interact 1998;24;111-112:1-14.

4. Antioxidant lozenge could help ward off flu. www.reutershealth.com (Accessed 19 April 2000).

5. Aw TY, Wierzbicka G, Jones DP. Oral glutathione increases tissue glutathione in vivo. Chem Biol Interact 1991;80:89-97. View abstract.

6. Bains JS, Shaw CA. Neurodegenerative disorders in humans: the role of glutathione in oxidative stress-mediated neuronal death. Brain Res Brain Res Rev 1997;25:335-58. View abstract.

7. Borok Z, Buhl R, Grimes GJ, et al. Effect of glutathione aerosol on an oxidant-antioxidant imbalance in idiopathic pulmonary fibrosis. Lancet 1991;338:215-6. View abstract.

Tumeric Extract

1. DiSilvestro, R. A., Joseph, E., Zhao, S., & Bomser, J. (2012). Diverse effects of a low dose supplement of lipidated curcumin in healthy middle-aged people. Nutrition Journal, 11(1), 1.

2. Chainani-Wu, N., Madden, E., Lozada-Nur, F., & Silverman, S. (2012). High-dose curcuminoids are efficacious in the reduction in symptoms and signs of oral lichen planus. Journal of the American Academy of Dermatology, 66(5), 752-760.

3. Belcaro, G., Cesarone, M. R., Dugall, M., Pellegrini, L., Ledda, A., Grossi, M. G., ... & Appendino, G. (2010). Efficacy and safety of Meriva®, a curcumin-phosphatidylcholine complex, during extended administration in osteoarthritis patients. Altern Med Rev, 15(4), 337-44.

4. Hanai, H., Iida, T., Takeuchi, K., Watanabe, F., Maruyama, Y., Andoh, A., ... & Yamada, M. (2006). Curcumin maintenance therapy for ulcerative colitis: randomized, multicenter, double-blind, placebo-controlled trial. Clinical Gastroenterology and Hepatology, 4(12), 1502-1506.

5. Di Pierro, F., Rapacioli, G., Di Maio, E. A., Appendino, G., Franceschi, F., & Togni, S. (2013). Comparative evaluation of the pain-relieving properties of a lecithinized formulation of curcumin (Meriva (®)), nimesulide, and acetaminophen. J Pain Res, 6, 201-205.

Alpha Lipoic Acid

1. McNeilly, A. M., Davison, G. W., Murphy, M. H., Nadeem, N., Trinick, T., Duly, E., ... & McEneny, J. (2011). Effect of α-lipoic acid and exercise training on cardiovascular disease risk in obesity with impaired glucose tolerance. Lipids in health and disease, 10(1), 1.

2. Zembron-Lacny, A., Slowinska-Lisowska, M., Szygula, Z., Witkowski, K., Stefaniak, T., & Dziubek, W. (2009). Assessment of the antioxidant effectiveness of alpha-lipoic acid in healthy men exposed to muscle-damaging exercise. J Physiol Pharmacol, 60(2), 139-43.

3. Sola, S., Mir, M. Q., Cheema, F. A., Khan-Merchant, N., Menon, R. G., Parthasarathy, S., & Khan, B. V. (2005). Irbesartan and lipoic acid improve endothelial function and reduce markers of inflammation in the metabolic syndrome results of the irbesartan and lipoic acid in endothelial dysfunction (island) study. Circulation, 111(3), 343-348.

4. Ranieri, M., Sciuscio, M., Cortese, A. M., Santamato, A., Di Teo, L., Ianieri, G., ... & Megna, M. (2009). The Use and Alpha-Lipoic Acid (ALA), Gamma Linolenic Acid (GLA) and Rehabilitation in the Treatment of Back Pain: Effect on Health-Related Quality of Life. International journal of immunopathology and pharmacology, 22(3 suppl), 45-50.

Dandelion Root

1. Lee et al. 2012; Effects of Taraxacum officinale on fatigue and immunological parameters in mice.

2. Jeon et al. 2008; the Anti-inflammatory activity of Taraxacum officinale.

3. Choi et al. 2010; Hypolipidemic and antioxidant effects of dandelion (Taraxacum officinale) root and leaf on cholesterol-fed rabbits.

4. Turski et al. 2011; Distribution, synthesis, and absorption of kynurenic acid in plants.

5. Domitrovic et al. 2010; Antifibrotic activity of Taraxacum officinale root in carbon tetrachloride-induced liver damage in mice.

6. Chatterjee et al 2011; The efficacy of dandelion root extract in inducing apoptosis in drug-resistant human melanoma cells. 7. Ovadje et al 2012; Efficient induction of extrinsic cell death by dandelion root extract in human chronic myelomonocytic leukemia (CMML) cells.

Uva-Ursi

1. Beaux D, Fleurentin J, Mortier F. Effect of extracts of Orthosiphon stamineus Benth, Hieracium pilosella L., Sambucus nigra L. and Arctostaphylos uva-ursi (L.) Spreng. in rats. Phytother Res. 1999;13(3):222-5.

2. Chauhan B, Yu C, Krantis A, Scott I, Arnason JT, Marles RJ, Foster BC. In vitro activity of uva-ursi against cytochrome P450 isoenzymes and P-glycoprotein. Can J Physiol Pharmacol. 2007;85(11):1099-107.

3. Grases F, Melero G, Costa-Bauza A, Prieto R, March JG Urolithiasis and phytotherapy. Int Urol Nephrol. 1994;26(5):507-11.

4. Head KA. Natural approaches to prevention and treatment of infections of the lower urinary tract. Altern Med Rev. 2008;13(3):227-44.

5. Larsson B, Jonasson A, Fianu S. Prophylactic effect of UVA-E in women with recurrent cystitis: a preliminary report. Curr Ther Res. 1993;53:441-3.

6. Matsuda H, Nakamura S, Tanaka T, Kubo M. [Pharmacological studies on leaf of arctostaphylos uva-ursi (L.) Spreng. V. Effects of water extract from arctostaphylos uva-ursi (L.) Spreng. (Bearberry leaf) on the antiallergic anti-inflammatory activities of dexamethasone ointment.] Yakugaku Zasshi - J Pharm Soc Jpn. 1992;112(9):673-7.

7. Matsuda H, Nakata H, Tanaka T, Kubo M. [a Pharmacological study on Arctostaphylos uva-ursi (L.) Spreng. II. Combined effects of arbutin and prednisolone or dexamethasone on immuno-inflammation] Yakugaku Zasshi. 1990;110(1):68-76.

L-Glycine

1. Wax, B., Hilton, L., Vickers, B., Gilliland, K., & Conrad, M. (2013). Effects of glycine-arginine-alpha-ketoisocaproic acid supplementation in college-age trained females during multi-bouts of resistance exercise. J Diet Suppl, 10(1), 6-16.

2. Nelson, M. J., Harris, M. B., Boluyt, M. O., Hwang, H. S., & Starnes, J. W. (2011). Effect of N-2-mercaptopropionyl glycine on exercise-induced cardiac adaptations. [Research Support, Non-U.S. Gov't]. Am J Physiol Regul Integr Comp Physiol, 300(4), R993-R1000..

3. Jacobs, P. L., & Goldstein, E. R. (2010). Long-term glycine propionyl-l-carnitine supplemention and paradoxical effects on repeated anaerobic sprint performance. J Int Soc Sports Nutr, 7, 35. doi: 10.1186/1550-2783-7-35

4. Bloomer, R. J., Tschume, L. C., & Smith, W. A. (2009). Glycine propionyl-L-carnitine modulates lipid peroxidation and nitric oxide in human subjects. [Randomized Controlled Trial Research Support, Non-U.S. Gov't]. Int J Vitam Nutr Res, 79(3), 131-141.

5. Jacobs, P. L., Goldstein, E. R., Blackburn, W., Orem, I., & Hughes, J. J. (2009). Glycine propionyl-L-carnitine produces enhanced anaerobic work capacity with reduced lactate accumulation in resistance trained males. J Int Soc Sports Nutr, 6, 9. doi: 10.1186/1550-2783-6-9

Juniper Berry

1. Bisset, NG. Juniper fructus. 1994;283-285.

2. Janku, I., Hava, M., and Motl, O. [Diuretic substance from juniper (Juniperus communis L.)]. Experientia 6-15-1957;13(6):255-256.

3. Stanic, G, Samarzija, I, and Blazevic, N. Time-dependent diuretic response in rats treated with juniper berry preparations. Phytother Res 1998;12:494-497.

Buchu Powder

1. Ernst E. Interactions between synthetic and herbal medicinal products Part 1: a systematic review of the indirect evidence. Perfusion 2000;13:4-15.

2. Lis-Balchin, M., Hart, S., and Simpson, E. Buchu (Agathosma betulina and A. crenulata, Rutaceae) essential oils: their pharmacological action on guinea-pig ileum and antimicrobial activity on microorganisms. J Pharm.Pharmacol. 2001;53(4):579-582

3. Fetrow CW, Avila JR. Professional's Handbook of Complementary & Alternative Medicines. 1st ed. Springhouse, PA: Springhouse Corp., 1999.

Artichoke Powder

1. Fintelmann V. Antidyspeptic and lipid-lowering effects of artichoke leaf extract - results of clinical studies into the efficacy and tolerance of Hepar-SL forte involving 553 patients. J Gen Med 1996;2:3-19.

2. Fintelmann V. Therapeutic profile and mechanism of action of artichoke leaf extract: hypolipemic, antioxidant, hepatoprotective and choleretic properties. Phytomedicine 1996;suppl 1:50.

3. Gebhardt R and Fausel M. Antioxidant and hepatoprotective effects of artichoke extracts and constituents in cultured rat hepatocytes. Toxicol in Vitro 1997;11:669-672.

4. Hammerl, H. and Pichler, O. [Possibility of causal treatment of bile duct diseases with an artichoke preparation.]. Wien.Med Wochenschr. 6-29-1957;107(25-26):545-546

5. Kiso, Y., Tohkin, M., and Hikino, H. Antihepatotoxic principles of Atractylodes rhizomes. J Nat.Prod. 1983;46(5):651-654

WARNING

California’s Proposition 65 entitles California consumers to special warnings.

WARNING: Cancer and Reproductive Harm - www.P65warnings.ca.gov/

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