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Insulin-sensitizing agents: metformin and thiazolidinedione derivatives

机译:胰岛素敏化剂:二甲双胍和噻唑烷二酮衍生物

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摘要

Both metformin and thiazolidinedione derivatives(TZDs) improve insulin resistance, a major pathogenesis of type 2 diabetes, and decrease blood glucose levels without stimulating insulin secretion. Metformin inhibits glucose output from the liver, while TZDs increase glucose utilization in the peripheral tissues. In addition, there has been indicated that these agents ameliorate metabolic syndrome beyond glucose-level lowering. Molecular targets of these agents have recently been revealed; AMP-activated protein kinase (AMPK) for metformin and adiponectin, while PPAR gamma for TZDs which induce gene expression of adipocyte glycerol kinase and adiponectin. Insulin-sensitizing agents are clinically useful for obese diabetic patients with insulin resistance. However, periodical examinations are necessary to avoid serious adverse effects such as lactic acidosis, although rare, by metformin and liver injury by TZDs.
机译:二甲双胍和噻唑烷二酮衍生物(TZDS)都改善了胰岛素抵抗,2型糖尿病的主要发病机制,并降低血糖水平而不刺激胰岛素分泌。 二甲双胍抑制来自肝脏的葡萄糖输出,而TZDS增加外周组织中的葡萄糖利用率。 此外,已经表明这些药剂改善了除葡萄糖水平降低之外的代谢综合征。 最近揭示了这些药剂的分子靶标; 用于二甲双胍和脂联素的AMP活化蛋白激酶(AMPK),而PPARγ用于诱导脂肪细胞甘油激酶和脂联素的基因表达的TZDS。 胰岛素敏化剂对患有胰岛素抵抗的肥胖患者临床上有用。 然而,期刊检查是必要的,以避免诸如乳酸中的严重不良反应,虽然通过TZDS的二甲双胍和肝损伤罕见。

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