共 89 条
PPARδ:: a dagger in the heart of the metabolic syndrome
被引:536
作者:

Barish, GD
论文数: 0 引用数: 0
h-index: 0
机构: Salk Inst Biol Studies, Howard Hughes Med Inst, Gene Express Lab, La Jolla, CA 92037 USA

Narkar, VA
论文数: 0 引用数: 0
h-index: 0
机构: Salk Inst Biol Studies, Howard Hughes Med Inst, Gene Express Lab, La Jolla, CA 92037 USA

Evans, RM
论文数: 0 引用数: 0
h-index: 0
机构: Salk Inst Biol Studies, Howard Hughes Med Inst, Gene Express Lab, La Jolla, CA 92037 USA
机构:
[1] Salk Inst Biol Studies, Howard Hughes Med Inst, Gene Express Lab, La Jolla, CA 92037 USA
[2] Univ Calif San Francisco, Dept Med, Div Endocrinol & Metab, San Francisco, CA 94143 USA
关键词:
D O I:
10.1172/JCI27955
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Obesity is a growing threat to global health by virtue of its association with insulin resistance, glucose intolerance, hypertension, and dyslipidemia, collectively known as the metabolic syndrome or syndrome X. The nuclear receptors PPAR alpha and PPAR gamma are therapeutic targets for hypertriglyceridemia and insulin resistance, respectively, and drugs that modulate these receptors are currently in clinical use. More recent work on the less-described PPAR isotype PPAR delta has uncovered a dual benefit for both hypertriglyceridemia and insulin resistance, highlighting the broad potential of PPAR delta in the treatment of metabolic disease. PPAR delta enhances fatty acid catabolism and energy uncoupling in adipose tissue and muscle, and it suppresses macrophage-derived inflammation. Its combined activities in these and other tissues make it a multifaceted therapeutic target for the metabolic syndrome with the potential to control weight gain, enhance physical endurance, improve insulin sensitivity, and ameliorate atherosclerosis.
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页码:590 / 597
页数:8
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