过氧化物酶体增殖物激活受体
PPAR激动剂
医学
受体
脂质代谢
氧化应激
炎症
核受体
吡格列酮
转录因子
药理学
内分泌学
内科学
糖尿病
过氧化物酶体
生物
2型糖尿病
生物化学
基因
作者
Ekaterina A. Ivanova,Veronika A. Myasoedova,Alexandra А. Melnichenko,Alexander Nikolaevich Orekhov
标识
DOI:10.2174/1381612823666161118145850
摘要
Peroxisome proliferation-activated receptors (PPARs) are ligand-activated transcription factors that mainly regulate genes responsible for fatty acid (FA) and energy metabolism. There are three members of the PPAR family, PPAR-α, PPAR- β/δ and PPAR-γ. All three isoforms have therapeutic potential for treatment of cardiovascular disorders, and PPAR agonists are currently being actively studied in pre-clinical and clinical trials. PPAR γ agonists, main tissue expressing isoform, have potential to influence on inflammation processes, reduce oxidative stress, improve endothelial function and plays an important role in lipid metabolism. PPAR-γ agonists are used as insulin sensitizers for treatment of diabetes; however, there is accumulating evidence that their clinical application can be broadened. The wide spectrum of PPAR-γ activation effects may be beneficial for treatment of various cardiovascular conditions as atherosclerosis, hypertension and aortic aneurysm, including surgical interventions. In this Review we will discuss the implication of PPAR-γ in the cardiovascular system and potential role of PPAR-γ agonists in treatment of conditions associated with high cardiovascular risks.
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