血管平滑肌PPARγ的抗炎机制。

Q3 Medicine
Masashi Mukohda, Hiroshi Ozaki
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引用次数: 2

摘要

本文综述了核转录因子-过氧化物酶体增殖体激活受体γ (PPARγ)在血管组织中的抗炎和保护作用的分子机制。PPARγ是一种普遍表达的核因子,在脂肪组织和炎症细胞中被充分研究。此外,血管PPARγ对动脉粥样硬化和血管重塑/功能障碍的有益作用已被报道,但其详细机制仍有待完全阐明。临床和基础研究表明,合成的PPARγ配体噻唑烷二酮(TZDs)对动脉粥样硬化等心血管疾病具有保护作用。最近利用遗传工具的研究表明,TZDs对心血管疾病的保护作用不是由于改善胰岛素抵抗的结果,而可能是由于对血管内皮细胞和平滑肌细胞中的PPARγ的直接影响。在这篇综述中,我们讨论了血管PPARγ调节血管炎症和重塑/功能障碍的机制,特别是在平滑肌细胞中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anti-inflammatory mechanisms of the vascular smooth muscle PPARγ.

Anti-inflammatory mechanisms of the vascular smooth muscle PPARγ.

This review highlights molecular mechanisms of anti-inflammatory and protective effects of the nuclear transcription factor, peroxisome proliferator-activated receptor γ (PPARγ) in vascular tissue. PPARγ is an ubiquitously expressed nuclear factor, and well-studied in adipose tissue and inflammatory cells. Additionally, beneficial effects of vascular PPARγ's on atherosclerosis and vascular remodeling/dysfunction have been reported although the detailed mechanism remains to be completely elucidated. Clinical and basic studies have shown that the synthetic PPARγ ligands, thiazolidinediones (TZDs), have protective effects against cardiovascular diseases such as atherosclerosis. Recent studies utilizing genetic tools suggested that those protective effects of TZDs on cardiovascular diseases are not due to a consequence of improvement of insulin resistance, but may be due to a direct effect on PPARγ's in vascular endothelial and smooth muscle cells. In this review, we discuss proposed mechanisms by which the vascular PPARγ regulates vascular inflammation and remodeling/dysfunction especially in smooth muscle cells.

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来源期刊
Journal of Smooth Muscle Research
Journal of Smooth Muscle Research Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
2.30
自引率
0.00%
发文量
7
审稿时长
10 weeks
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