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Wedelolactone, a plant coumarin, prevents vascular smooth muscle cell proliferation and injury-induced neointimal hyperplasia through Akt and AMPK signaling

机译:Wedelolactere,一种植物香豆素,通过AKT和AMPK信号传导阻止血管平滑肌细胞增殖和损伤诱导的新内膜增生

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Wedelolactone (WDL) is a natural compound derived from Chinese herbal medicine Eclipta prostrate L, and has been reported to exhibit various effects potentially beneficial for human health. However, the possible preventive effects of WDL toward vascular remodeling and mechanisms involved have not been investigated to date. In this study, we investigated the effects of WDL on proliferation induced by platelet-derived growth factor (PDGF) in primary rat aortic smooth muscle cells (VSMCs) and on neointimal hyperplasia resulted from balloon injury in rats. WDL exhibited strong inhibitory effects against PDGF-induced VSMC proliferation. Cell cycle analysis revealed that WDL induced G0/G1 arrest and prevented cell cycle from entering S phase. Immunoblot analysis suggested that the cell cycle arrest induced by WDL was through Akt suppression and adenosine 5'-monophosphate-activated protein kinase (AMPK) activation, with a subsequent cyclin-dependent kinase inhibitor p21 induction and cyclin D1 inhibition. We also observed that WDL notably reduced neointima-to-media area ratio of balloon injured rat common carotid arteries (CCAs) in comparison with those untreated balloon-injured CCAs. The regulation of WDL on protein expressions of Akt, AMPK and cyclin D1 in vivo were also consistent with that in vitro. Taken together, our results suggest WDL exhibits potential preventive effects toward vascular remodeling and neointimal hyperplasia through the reduction of VSMC proliferation via inhibition of Akt and activation of AMPK. (C) 2017 Elsevier Inc. All rights reserved.
机译:Wedelolone(WDL)是衍生自中草药Eclipta Prostrate L的天然化合物,并据报道,据报道潜在有利于人类健康的各种影响。然而,WDL对血管重塑的可能预防效果和所涉及的机制迄今尚未调查。在这项研究中,我们研究了WDL对原发性大鼠主动脉平滑肌细胞(VSMC)中的血小板衍生生长因子(PDGF)和对大鼠气球损伤导致的新内膜增生引起的增殖的影响。 WDL对PDGF诱导的VSMC增殖表现出强烈的抑制作用。细胞循环分析显示,WDL诱导G0 / G1抑制和预防细胞周期进入S期。免疫印迹分析表明,WDL诱导的细胞周期停滞通过Akt抑制和腺苷5'-单磷酸活化的蛋白激酶(AMPK)活化,随后的细胞周期依赖性激酶抑制剂P21诱导和细胞周期蛋白D1抑制。我们还观察到,与那些未处理的气球损伤的CCA相比,WDL显着降低了气囊受伤大鼠常见颈动脉(CCAS)的内部介质面积比。在体内测定AKT,AMPK和细胞周期蛋白D1的蛋白质表达的调节也与体外相一致。我们的结果表明WDL通过抑制AKT和AMPK的激活,通过减少VSMC增殖对血管重塑和新内膜增生表现出潜在的预防作用。 (c)2017年Elsevier Inc.保留所有权利。

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