Fuior Elena Valeria, Zvintzou Evangelia, Filippatos Theodosios, Giannatou Katerina, Mparnia Victoria, Simionescu Maya, Gafencu Anca Violeta, Kypreos Kyriakos E
Institute of Cellular Biology and Pathology, "Nicolae Simionescu" of the Romanian Academy, 050568 Bucharest, Romania.
Pharmacology Laboratory, Department of Medicine, University of Patras, 26500 Rio Achaias, Greece.
Biomedicines. 2023 Oct 3;11(10):2696. doi: 10.3390/biomedicines11102696.
Peroxisome proliferator-activated receptors (PPARs) are a group of ligand-binding transcription factors with pivotal action in regulating pleiotropic signaling pathways of energetic metabolism, immune responses and cell proliferation and differentiation. A significant body of evidence indicates that the PPARα receptor is an important modulator of plasma lipid and lipoprotein metabolism, with pluripotent effects influencing the lipid and apolipoprotein cargo of both atherogenic and antiatherogenic lipoproteins and their functionality. Clinical evidence supports an important role of PPARα agonists (fibric acid derivatives) in the treatment of hypertriglyceridemia and/or low high-density lipoprotein (HDL) cholesterol levels, although the effects of clinical trials are contradictory and point to a reduction in the risk of nonfatal and fatal myocardial infarction events. In this manuscript, we provide an up-to-date critical review of the existing relevant literature.
过氧化物酶体增殖物激活受体(PPARs)是一组配体结合转录因子,在调节能量代谢、免疫反应以及细胞增殖和分化的多效性信号通路中起关键作用。大量证据表明,PPARα受体是血浆脂质和脂蛋白代谢的重要调节因子,具有多能效应,可影响致动脉粥样硬化脂蛋白和抗动脉粥样硬化脂蛋白的脂质和载脂蛋白成分及其功能。临床证据支持PPARα激动剂(贝特类衍生物)在治疗高甘油三酯血症和/或低高密度脂蛋白(HDL)胆固醇水平方面的重要作用,尽管临床试验的结果相互矛盾,且表明非致命和致命心肌梗死事件的风险有所降低。在本手稿中,我们对现有相关文献进行了最新的批判性综述。