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靶向核激素受体:过氧化物酶体增殖物激活受体α激动剂作为类风湿关节炎潜在的疾病改善药物

Targeting Nuclear Hormone Receptors: PPARα Agonists as Potential Disease-Modifying Drugs for Rheumatoid Arthritis.

作者信息

Shirinsky Ivan V, Shirinsky Valery S

机构信息

Laboratory of Clinical Immunopharmacology, Scientific Research Institute of Clinical Immunology, RAMS, 14 Yadrintsevskaya Street, Novosibirsk 630099, Russia.

出版信息

Int J Rheumatol. 2011;2011:937843. doi: 10.1155/2011/937843. Epub 2011 Jun 21.

Abstract

In recent years, peroxisome proliferator-activated receptors (PPARs) have received growing interest due to the broad spectrum of their biological activities. PPARα, an isoform of PPAR, plays an important role in lipid homeostasis and inflammation, which makes it a potential target for the treatment of chronic inflammatory disorders, including RA. This paper reviews studies on the properties of PPARα agonists which may be pertinent to the treatment of RA. These properties include effects on lipid metabolism, inflammation, and angiogenesis, as well as interference with glucocorticoid effects, and a potential role in gender dimorphism of autoimmune disorders. However, current clinical experience with this class of drugs in RA is limited. New studies are needed to elucidate whether PPARα agonism may be an effective treatment strategy for RA patients.

摘要

近年来,过氧化物酶体增殖物激活受体(PPARs)因其广泛的生物学活性而受到越来越多的关注。PPARα作为PPAR的一种亚型,在脂质稳态和炎症中发挥着重要作用,这使其成为治疗包括类风湿关节炎(RA)在内的慢性炎症性疾病的潜在靶点。本文综述了可能与RA治疗相关的PPARα激动剂特性的研究。这些特性包括对脂质代谢、炎症和血管生成的影响,以及对糖皮质激素作用的干扰,还有在自身免疫性疾病性别差异中的潜在作用。然而,目前这类药物在RA中的临床经验有限。需要开展新的研究来阐明PPARα激动作用是否可能成为RA患者的有效治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c89/3134189/5082f59b30ca/IJR2011-937843.001.jpg

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