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AAS liver therapy

GawdsGift

New member
i am reading alot about AAs liver therapy and was wondering if these drugs would work for people with liver diseases such as sarosis and or hepatitus c???

my mother has hep c which attacks her liver and is in need of a liver transplant or partial liver t-plant. would any of these meds help her with liver stress from the chemotherapy she takes??? she takes interferon i belive its spelled,. i know this isnt a AAs topic but we do discuss liver therapy ALOT, and if one of these drugs could help my mother out, WOW. i'd be in debt forever. if any one with a medical background or links to informartion regarding this topic cold let me in on some knowledge that would be great. MUCHHHHHH KARMA
 
Med Klin 1999 Oct 15;94 Suppl 3:84-9 Related Articles, Links


A conservative triple antioxidant approach to the treatment of hepatitis C. Combination of alpha lipoic acid (thioctic acid), silymarin, and selenium: three case histories.

Berkson BM.

Integrative Medical Center of New Mexico, New Mexico State University, Las Cruces, USA. [email protected]

BACKGROUND: There has been an increase in the number of adults seeking liver transplantation for hepatitis C in the last few years and the count is going up rapidly. There is no reliable and effective therapy for chronic hepatitis C since interferon and antivirals work no more than 30% of the time, and liver transplant surgery is uncertain and tentative over the long run. This is because, ultimately, residual hepatitis C viremia infects the new liver. Furthermore, liver transplantation can be painful, disabling and extremely costly. TREATMENT PROGRAM: The author describes a low cost and efficacious treatment program in 3 patients with cirrhosis, portal hypertension and esophageal varices secondary to chronic hepatitis C infection. This effective and conservative regimen combines 3 potent antioxidants (alpha-lipoic acid [thioctic acid], silymarin, and selenium) that possess antiviral, free radical quenching and immune boosting qualities. CONCLUSION: There are no remarkably effective treatments for chronic hepatitis C in general use. Interferon and antivirals have less than a 30% response rate and because of the residual viremia, a newly transplanted liver usually becomes infected again. The triple antioxidant combination of alpha-lipoic acid, silymarin and selenium was chosen for a conservative treatment of hepatitis C because these substances protect the liver from free radical damage, increase the levels of other fundamental antioxidants, and interfere with viral proliferation. The 3 patients presented in this paper followed the triple antioxidant program and recovered quickly and their laboratory values remarkably improved. Furthermore, liver transplantation was avoided and the patients are back at work, carrying out their normal activities, and feeling healthy. The author offers a more conservative approach to the treatment of hepatitis C, that is exceedingly less expensive. One year of the triple antioxidant therapy described in this paper costs less than $2,000, as compared to mor than $300,000 a year for liver transplant surgery. It appears reasonable, that prior to liver transplant surgery evaluation, or during the transplant evaluation process, the conservative triple antioxidant treatment approach should be considered. If these is a significant betterment in the patient's condition, liver transplant surgery may be avoided.


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Med Klin 1976 Oct 22;71(43):1831-5 Related Articles, Links


[A contribution to the treatment of chronic liver diseases (author's transl)]

[Article in German]

Moller E, Schmitt R.

89 randomized liver patients (42 with chronic hepatitis, 25 with hepatic cirrhosis, 14 with hepatitis of protracted evolution, 8 with alcohol-toxic adiposis hepatica, stage II) are reported, in whom considerable functionally and histologically identifiable therapeutic results were achieved by combined i.v. and oral treatment with thioctic acid. According to expectation, the most favourable results were found in alcohol-conditioned chronic liver diseases; however, also in chronic active hepatitis, resistant to treatment, a therapy could be promising. The oral therapy with thioctic acid, producing no side effects, is especially suited for the long-term outpatient treatment of chronic hepatitis and hepatic cirrhosis of toxic and posthepatic etiology.
 
CREDIT: YellowJacket

N-acetyl Cysteine Profile
by YellowJacket

N-acetyl Cysteine (NAC) is a very intriguing and underrated supplement. When one thinks of protecting his or her liver from 17-alpha alkylated steroids, alpha lipoic acid (ala) or milk thistle (silymarin) comes to mind, but NAC is possibly more beneficial than either of these liver aids. NAC is derived from the amino acid L-Cysteine and a precursor to Glutathione. NAC is metabolized into glutathione upon entry to the body. Glutathione is a protein found within cells and acts as the 'captain' of the body's antioxidant army. Glutathione hunts down free radicals and neutralizes their harmful effects. Glutathione also acts as a detoxifier and has the ability to alter chemical structures so they become neutral or less harmful. Glutathione is capable of removing any excess of heavy metals like mercury and lead, thus promoting a healthier liver.

NAC and its myriad uses go beyond liver protection and antioxidant capabilites. NAC isomer can act as a radioprotectant against many aspects of oxidative damage (1). NAC has been used in emergency rooms for sometime to counteract posion ingestion, especially arsenic poisoning in humans. In this study, a 32- year old male had ingested 900mgs of arsenic in attempts to take his life, but N-acetylcysteine intravenously had been given and the man was discharged 24 hours later (2). NAC in high oral doses is used to prevent and treat Influenza infection and is used in even higher doses to boost the immune system of those who live with Immune Deficiency Syndrome (AIDS). Lack of GSH and electrophilic/oxidative injury have been identified among the causes of the adult respiratory distress syndrome (ARDS), idiopathic pulmonary fibrosis (IPF), and the acquired immunodeficiency syndrome (AIDS) [/](3)[/I]. HIV-infected persons at all stages of the disease were found to have decreased plasma cystine and cysteine concentrations and decreased intracellular glutathione levels (4) . The use in treatment of AIDS patients are particularly interesting and seems to be a staple in all treatment regimens for its immune boosting effects. L-Glutamine is often used in treatment and supplemented by those with AIDS to boost immune function. NAC seems to have been lost in importance by those who weight train and participate in endurance activities. NAC is also effective in fighting tumor formation and growth. In one study, NAC treatment decreased the weight of a locally formed primary tumor and produced a dose-related delay in tumor formation (5). Although dose amounts were given, the NAC was taken orally.

NAC is also used to fight the harmful effects of tobacco on the cell. It was showed that cigarette smoke reduces cell deformability, increasing the difficulty experienced by the larger neutrophils in negotiating the smaller capillary segments, so delaying their passage during smoking. This effect is both diminished and recoverable by the addition of plasma, and by GSH in concentrations found in plasma. (6)

For liver protection and anti-oxidant purposes, a dose of 600mg can be used daily and works well in conjunction with milk thistle as a preventitive measure. There are no known contraindications or drug interactions with NAC.

(1) Free Radic Biol Med. 2003 Mar 15;34(6):689-95. Antioxidant role of N-acetyl cysteine isomers following high dose irradiation. Neal R, Matthews RH, Lutz P, Ercal N. Department of Chemistry, University of Missouri.

(2) Martin D, Willis S, Cline D. N-Acetylcysteine In The Treatment Of Human Arsenic Poisoning. J Am Board Fam Pract 3:293-296;1990

(3) Ruffmann R Wendel A. GSH rescue by N-acetylcysteine. In: Klin Wochenschr (1991 Nov 15) 69(18):857-62

(4)Droge W. Cysteine and glutathione deficiency in AIDS patients: a rationale for the treatment with N-acetyl-cysteine. In: Pharmacology (1993) 46(2):61-5

(5) De Flora S. Inhibition of invasion, gelatinase activity, tumor take and metastasis of malignant cells by N-acetylcysteine. In: Int J Cancer (1995 Mar 29) 61(1):121-9

(6) MacNee W Bridgeman MM Marsden M Drost E Lannan S Selby C Donaldson K. The effects of N-acetylcysteine and glutathione on smoke-induced changes in lung phagocytes and epithelial cells. In: Am J Med (1991 Sep 30) 91(3C):60S-66S

Article by YellowJacket. YellowJacket is a moderator at Superior Muscle, Steroid Support and Competitive Muscle
 
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