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吡格列酮通过脂联素依赖和非依赖途径改善袖套诱导的血管平滑肌细胞增殖形成的新内膜。

Pioglitazone Ameliorates Smooth Muscle Cell Proliferation in Cuff-Induced Neointimal Formation by Both Adiponectin-Dependent and -Independent Pathways.

机构信息

Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan.

Laboratory for Metabolic Homeostasis, RIKEN Center for Integrative Medical Sciences, Kanagawa, 230-0045, Japan.

出版信息

Sci Rep. 2016 Oct 5;6:34707. doi: 10.1038/srep34707.

Abstract

The aim of this study is to elucidate to what degree adiponectin is involved in TZD-mediated amelioration of neointimal formation. We investigated the effect of 3- or 8-weeks' pioglitazone on cuff-induced neointimal formation in adiponectin-deficient (APN-KO) and wild-type (WT) mice. Pioglitazone for 3 weeks reduced neointimal formation in the WT mice with upregulation of the plasma adiponectin levels, but failed to reduce neointimal formation in the APN-KO mice, suggesting that pioglitazone suppressed neointimal formation by adiponectin-dependent mechanisms. Pioglitazone for 3 weeks suppressed vascular smooth muscle cell (VSMC) proliferation and increased AdipoR2 expression in the WT mice. In vitro, globular adiponectin activated AMPK through both AdipoR1 and AdipoR2, resulting in the inhibition of VSMC proliferation. Interestingly, 8-weeks' pioglitazone was reduced neointimal formation in APN-KO mice to degree similar to that seen in the WT mice, suggesting that pioglitazone can also suppress neointimal formation via a mechanism independent of adiponectin. Pioglitazone for 8 weeks completely abrogated the increased VSMC proliferation, along with a reduction of cyclin B1 and cyclin D1 expressions and cardiovascular risk profile in the APN-KO mice. In vitro, pioglitazone suppressed these expressions, leading to inhibition of VSMC proliferation. Pioglitazone suppresses neointimal formation via both adiponectin-dependent and adiponectin-independent mechanisms.

摘要

本研究旨在阐明脂联素在噻唑烷二酮类药物改善内膜新生中的作用程度。我们研究了 3 或 8 周吡格列酮对脂联素缺乏(APN-KO)和野生型(WT)小鼠套管诱导内膜新生的影响。3 周吡格列酮可使 WT 小鼠的血浆脂联素水平升高,从而减少内膜新生,但不能减少 APN-KO 小鼠的内膜新生,表明吡格列酮通过脂联素依赖机制抑制内膜新生。3 周吡格列酮可抑制 WT 小鼠血管平滑肌细胞(VSMC)增殖并增加 AdipoR2 表达。在体外,球状脂联素通过 AdipoR1 和 AdipoR2 激活 AMPK,从而抑制 VSMC 增殖。有趣的是,8 周吡格列酮可使 APN-KO 小鼠的内膜新生减少至与 WT 小鼠相似的程度,表明吡格列酮也可通过非脂联素依赖机制抑制内膜新生。8 周吡格列酮可完全消除 APN-KO 小鼠中 VSMC 增殖增加,以及 cyclin B1 和 cyclin D1 表达减少和心血管风险特征,在体外,吡格列酮抑制这些表达,从而抑制 VSMC 增殖。吡格列酮通过脂联素依赖和非脂联素依赖机制抑制内膜新生。

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