Université de Lille, INSERM, CHU Lille, Institut Pasteur de Lille, U1011-EGID, F-59000 Lille, France.
International Institute of Molecular and Cell Biology, 4 Ks. Trojdena Street, 02-109 Warsaw, Poland.
Nat Rev Endocrinol. 2017 Jan;13(1):36-49. doi: 10.1038/nrendo.2016.135. Epub 2016 Sep 16.
Obesity is a worldwide epidemic that predisposes individuals to cardiometabolic complications, such as type 2 diabetes mellitus (T2DM) and nonalcoholic fatty liver disease (NAFLD), which are all related to inappropriate ectopic lipid deposition. Identification of the pathogenic molecular mechanisms and effective therapeutic approaches are highly needed. The peroxisome proliferator-activated receptors (PPARs) modulate several biological processes that are perturbed in obesity, including inflammation, lipid and glucose metabolism and overall energy homeostasis. Here, we review how PPARs regulate the functions of adipose tissues, such as adipogenesis, lipid storage and adaptive thermogenesis, under healthy and pathological conditions. We also discuss the clinical use and mechanism of PPAR agonists in the treatment of obesity comorbidities such as dyslipidaemia, T2DM and NAFLD. First generation PPAR agonists, primarily those acting on PPARγ, are associated with adverse effects that outweigh their clinical benefits, which led to the discontinuation of their development. An improved understanding of the physiological roles of PPARs might, therefore, enable the development of safe, new PPAR agonists with improved therapeutic potential.
肥胖是一种全球性的流行疾病,使个体易患代谢并发症,如 2 型糖尿病(T2DM)和非酒精性脂肪性肝病(NAFLD),这些疾病都与异位脂质沉积不当有关。因此,迫切需要确定致病的分子机制和有效的治疗方法。过氧化物酶体增殖物激活受体(PPARs)调节多种在肥胖中受到干扰的生物学过程,包括炎症、脂质和葡萄糖代谢以及整体能量稳态。在这里,我们综述了 PPARs 如何在健康和病理条件下调节脂肪组织的功能,如脂肪生成、脂质储存和适应性产热。我们还讨论了 PPAR 激动剂在治疗肥胖相关疾病(如血脂异常、T2DM 和 NAFLD)中的临床应用和作用机制。第一代 PPAR 激动剂主要作用于 PPARγ,与临床益处相比,其不良反应更为严重,这导致了它们的开发被终止。因此,对 PPARs 生理作用的深入了解可能会促进安全、新型、具有更好治疗潜力的 PPAR 激动剂的开发。