2型糖尿病
医学
胰岛素抵抗
胰岛素
血糖性
糖尿病
罗格列酮
药理学
不利影响
胰岛素敏感性
敏化
生物信息学
内科学
内分泌学
生物
免疫学
作者
Raymond E. Soccio,Eric R. Chen,Mitchell A. Lazar
出处
期刊:Cell Metabolism
[Cell Press]
日期:2014-10-01
卷期号:20 (4): 573-591
被引量:423
标识
DOI:10.1016/j.cmet.2014.08.005
摘要
Type 2 diabetes is caused by insulin resistance coupled with an inability to produce enough insulin to control blood glucose, and thiazolidinediones (TZDs) are the only current antidiabetic agents that function primarily by increasing insulin sensitivity. However, despite clear benefits in glycemic control, this class of drugs has recently fallen into disuse due to concerns over side effects and adverse events. Here we review the clinical data and attempt to balance the benefits and risks of TZD therapy. We also examine potential mechanisms of action for the beneficial and harmful effects of TZDs, mainly via agonism of the nuclear receptor PPARγ. Based on critical appraisal of both preclinical and clinical studies, we discuss the prospect of harnessing the insulin sensitizing effects of PPARγ for more effective, safe, and potentially personalized treatments of type 2 diabetes.
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