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      Metformin reverses fatty liver disease in obese, leptin-deficient mice.

      Nature medicine
      Adenosine Triphosphate, metabolism, Adipose Tissue, drug effects, Animals, Body Weight, Energy Intake, Energy Metabolism, Fatty Liver, drug therapy, Hepatomegaly, Homeostasis, Hypoglycemic Agents, therapeutic use, Insulin Resistance, Lipids, biosynthesis, Metformin, Mice, Mice, Obese, Obesity, Transaminases, Tumor Necrosis Factor-alpha

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          Abstract

          There is no known treatment for fatty liver, a ubiquitous cause of chronic liver disease. However, because it is associated with hyperinsulinemia and insulin-resistance, insulin-sensitizing agents might be beneficial. To evaluate this possibility, insulin-resistant ob/ob mice with fatty livers were treated with metformin, an agent that improves hepatic insulin-resistance. Metformin improved fatty liver disease, reversing hepatomegaly, steatosis and aminotransferase abnormalities. The therapeutic mechanism likely involves inhibited hepatic expression of tumor necrosis factor (TNF) alpha and TNF-inducible factors that promote hepatic lipid accumulation and ATP depletion. These findings suggest a mechanism of action for metformin and identify novel therapeutic targets in insulin-resistant states.

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