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首页> 外文期刊>International journal of molecular medicine >High glucose upregulates endothelin type B receptors in vascular smooth muscle cells via the downregulation of Sirt1
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High glucose upregulates endothelin type B receptors in vascular smooth muscle cells via the downregulation of Sirt1

机译:高葡萄糖通过SIRT1的下调将血管平滑肌细胞中的内皮素型B受体上调

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摘要

Silent information regulator family protein 1 (Sirt1) has recently gained attention for its protective effects against diabetic and cardiovascular diseases (CVDs). Vascular smooth muscle endothelin type B (ETB) receptors are involved in the pathogenesis of CVDs and diabetes. The aim of present study was to explore whether Sirt1 is involved in high glucose (HG)-mediated regulation of ETB receptors in rat superior mesenteric arteries (SMA). The rat SMA segments were cultured in the presence and absence of HG with or without the activator of Sirt1 and specific inhibitor for the extracellular signal-regulated protein kinase 1/2 (ERK1/2) for 24 h. Following organ culture, the contractile responses to sarafotoxin 6c were studied using a sensitive myograph, and the ETB receptor protein expression level was determined using western blotting. The results demonstrated that HG induced upregulation of ETB receptor expression and increased receptor-mediated vasoconstriction in SMA. Resveratrol (Res; a Sirt1 activator) concentration-dependently inhibited the HG-induced upregulation of ETB receptor expression and receptor-mediated vasoconstriction. Additionally, these effects could also be abolished by an inhibitor of the ERK1/2 signaling pathway. Furthermore, upregulation of ERK1/2 phosphorylation induced by HG was inhibited by Res. In conclusion, HG upregulated ETB receptors by downregulating Sirt1 and subsequently activating the ERK1/2 signaling pathways in the organ culture SMA.
机译:无声信息调节器家庭蛋白1(SIRT1)最近对糖尿病和心血管疾病(CVDS)的保护作用进行了关注。血管平滑肌内皮素B(ETB)受体参与CVDS和糖尿病的发病机制。本研究的目的是探讨SIRT1是否参与大鼠高级肠系膜(SMA)中的ETB受体的高葡萄糖(Hg)介导的调节。在具有或不具有SIRT1的活化剂和细胞外信号调节蛋白激酶1/2(ERK1 / 2)的特异性抑制剂的情况下在存在和不存在Hg的情况下培养大鼠SMA段。在器官培养之后,使用敏感的象形图研究了对Sarafotoxin 6c的收缩反应,使用Western印迹测定ETB受体蛋白表达水平。结果表明,Hg诱导η上的ETB受体表达和SMA中增加的受体介导的血管收缩。白藜芦醇(RES; SIRT1活化剂)浓度依赖性抑制ETB受体表达和受体介导的血管收缩的HG诱导的上调。另外,这些效应也可以通过ERK1 / 2信号传导途径的抑制剂废除。此外,REC抑制了Hg诱导的ERK1 / 2磷酸化的上调。总之,通过下调SIRT1并随后在器官培养SMA中激活ERK1 / 2信号传导途径,HG上调ETB受体。

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