4.5 Review Book Chapter

Methionine metabolism and liver disease

期刊

ANNUAL REVIEW OF NUTRITION
卷 28, 期 -, 页码 273-293

出版社

ANNUAL REVIEWS
DOI: 10.1146/annurev.nutr.28.061807.155438

关键词

S-adenosylmethionine; S-adenosylhomocysteine; folate cycle; transsulfuration pathway; fatty liver disease; hepatocellular carcinoma

资金

  1. NIH [AA12677, AA13847, AT1576]
  2. PN I+D SAF [2005-00855]
  3. HEPADIP-EULSHM-CT-205
  4. ETORTEK
  5. BBVA Foundation
  6. Program Ramon y Cajal and Fundacion La Caixa
  7. Instituto de Salud Carlos III
  8. [DK51719]
  9. National Center for Complementary & Integrative Health [R01AT001576] Funding Source: NIH RePORTER
  10. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK051719] Funding Source: NIH RePORTER
  11. NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM [R01AA013847, R01AA012677] Funding Source: NIH RePORTER

向作者/读者索取更多资源

In the early 1930s, Banting and Best, the discoverers of insulin, found that choline could prevent the development of fatty liver disease (steatosis) in pancreatectomized clogs treated with insulin. Later work indicated that in rats and mice, diets deficient in labile methyl groups (choline, methionine, betaine, folate) produced fatty liver and that long-term administration of diets deficient in choline and methionine also caused hepatocellular carcinoma. These experiments not only linked steatosis and diabetes but also provided evidence, for the first time, of the importance of labile methyl group balance to maintain normal liver function. This conclusion is now amply supported by the observation of mice devoid of key enzymes of methionine and folate metabolism and in patients with severe deficiencies in these enzymes. Moreover, treatments with various methionine metabolites in experimental animal models of liver disease show hepatoprotective properties.

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