|
|||||||
|
Liver SAP is effective in the management of various liver pathologies including Hepatitis B and C, inflammation, cirrhosis, fatty accumulation, and hepatocellular carcinoma and protect against the toxic effects of alcohol and certain pharmaceutical agents.
Liver SAP is effective in stimulating liver function and regeneration in detoxification protocols. Restoration of optimal liver function through the use of Liver SAP may positively affect digestion, skin quality, regulation of blood glucose and lipid levels, and hormone balance.
Milk Thistle (Silybum marianum) (80% silymarin) - 250 mg
Curcumin (Curcuma longa) (95% curcuminoids) -125 mg
Alpha-lipoic acid -100 mg
Artichoke (Cynara scolymus) (5% cynarins) - 50 mg
Dandelion (Taraxacum officinale) (3% flavonoids)- 50 mg
Schizandra (Schizandra chinensis) (9% schizandrins) - 50 mg
Calcium d-glucarate - 50 mg
L-methionine - 50 mg
N-Acetylcysteine - 25 mg
The liver is the largest glandular organ in the body with numerous vital functions including glucose, fat and protein metabolism, regulation of blood sugar levels, storage of vitamins, and digestion. It is also one of the major organs of detoxification, playing a key role in the neutralization of external substances such as drugs and alcohol, processing metabolic waste, and breaking down insulin and other hormones. The liver also has the unique property of being the only internal organ in the body capable of regeneration. Liver SAP contains a blend of high-quality botanical extracts and nutraceuticals that support liver function, protect against hepatotoxicity, and encourage re-growth of damaged hepatocytes.
90 capsules and 180 capsules
Take 2-6 capsules daily depending on desired out come of treatment. General support 1-3capsules/day To support detoxification 4-6 capsules/day
1. Ross S. 2008. Holist Nurs Pract, 22(5):299-300.
2. Tamayo C, Diamond S. 2007. Integr Cancer Ther, 6(2):146-57.
3. Polyak S, Morishima C, Shuhart M, Wang C, Liu Y, Lee D. 2007. Gastroenterology,132(5):1925-36.
4. Bares J, Berger J, Nelson J, Messner D, Schildt S, Standish L, Kowdley K. 2008. J Clin Gastroenterol, 42(8):937-44.
5. Itokawa H, Shi Q, Akiyama T, Morris-Natschke S, Lee K. 2008. Chin Med, 17;3:11.
6. Reyes-Gordillo K, Segovia J, Shibayama M, Tsutsumi V, Vergara P, Moreno M, Muriel P. 2008. Fundam Clin Pharmacol, 22(4):417-27.
7. Simbula G, Columbano A, Ledda-Columbano G, Sanna L, Deidda M, Diana A, Pibiri M. 2007. Apoptosis, 12(1):113-23.
8. Miccadei S, Di Venere D, Cardinali A, Romano F, Durazzo A, Foddai M, Fraioli R, Mobarhan S, Maiani G. 2008. Nutr Cancer, 60(2):276-83.
9. Loo W, Cheung M, Chow L. 2007. Biomed Pharmacother, 61(9):606-10.
10. SchÜtz K, Carle R, Schieber A. 2006. J Ethnopharmacol, 107(3):313-23.
11. Lu Y, Chen D. 2008. J Chromatogr A. EPub Sep 26.
12. Dodd S, Dean O, Copolov D, Malhi G, Berk M. 2008. Expert Opin Biol Ther, 8(12):1955-62.
13. MehmetÇik G, Ozdemirler G, KoÇak-Toker N, Cevikba U, Uysal M. 2008. Exp Toxicol Pathol, 60(6):475-80.
14. Selvakumar E, Prahalathan C, Mythili Y, Varalakshmi P. 2005. Mol Cell Biochem, 272(1-2):179-85.
15. Abdel-Zaher A, Abdel-Hady R, Mahmoud M, Farrag M. 2008. Toxicology, 243(3):261-70.
16. Terneus M, Brown J, Carpenter A, Valentovic M. 2008. Toxicology, 244(1):25-34.
17. Eminzade S, Uraz F, Izzettin F. 2008. Nutr Metab (Lond), 5:18.
18. Adhvaryu M, Reddy N, Vakharia B. 2008. World J Gastroenterol, 14(30):4753-62.
19. Duenschede F, Erbes K, Kircher A, Westermann S, Schad A, Riegler N, Ewald P, Dutkowski P, Kiemer A, Kempski O, Junginger T. 2007. Shock, 27(6):644-51.
20. Sener G, Tosun O, Sehirli A, KaÇmaz A, Arbak S, Ersoy Y, Ayano lu-DÜlger G. 2003. Life Sci, 72(24):2707-18.
21. Santiago F, Bueno P, Olmedo C, Muffak-Granero K, Comino A, Serradilla M, Mansilla A, Villar J, Garrote D, FerrÓn J. 2008. Transplant Proc, 40(9):2978-80.
22. Pan S, Dong H, Zhao X, Xiang C, Fang H, Fong W, Yu Z, Ko K. 2008. J Pharm Pharmacol, 60(3):399-403.
23. Baumgardner J, Shankar K, Hennings L, Albano E, Badger T, Ronis M. 2008. J Nutr, 138(10):1872-9.
24. de Oliveira C, Stefano J, de Siqueira E, Silva L, de Campos Mazo D, Lima V, Furuya C, Mello E, Souza F, Rabello F, Santos T, Nogueira M, Caldwell S, Alves V, Carrilho F. 2008. Hepatol Res, 38(2):159-65.
25. Park K, Min A, Koh E, Kim H, Kim M, Park H, Kim Y, Yoon T, Jang B, Hwang J, Kim J, Choi H, Park J, Lee I, Lee K. 2008. Hepatology, 48(5):1477-86.
26. Loguercio C, Federico A, Trappoliere M, Tuccillo C, de Sio I, Di Leva A, Niosi M, D'Auria M, Capasso R, Del Vecchio Blanco C; Real Sud Group. 2007. Dig Dis Sci, 52(9):2387-95.
27. Melhem A, Stern M, Shibolet O, Israeli E, Ackerman Z, Pappo O, Hemed N, Rowe M, Ohana H, Zabrecky G, Cohen R, Ilan Y. 2005. J Clin Gastroenterol, 39(8):737-42.
28. Yoysungnoen P, Wirachwong P, Changtam C, Suksamrarn A, Patumraj S. 2008. World J Gastroenterol, 14(13):2003-9.
Disclaimer: This content is subject to change. The information is intended to inform and educate; it does not replace the medical evaluation, advice, diagnosis or treatment by a healthcare professional. www.nhpassist.com © 2014 NDAssist Inc. and/or its affiliates. All rights reserved.
![]() |
Liver SAP
Indications Liver SAP is effective in the management of various liver pathologies including Hepatitis B and C, inflammation, cirrhosis, fatty accumulation, and hepatocellular carcinoma and protect against the toxic effects of alcohol and certain pharmaceutical agents. IngredientsMilk Thistle (Silybum marianum) (80% silymarin) - 250 mg Quantity
DoseTake 2-6 capsules daily depending on desired out come of treatment. General support 1-3capsules/day To support detoxification 4-6 capsules/day |
---|