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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Resveratrol down-regulates endothelin type B receptors in vascular smooth muscle cells via Sirt1/ERK1/2/NF-kappa B signaling pathways
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Resveratrol down-regulates endothelin type B receptors in vascular smooth muscle cells via Sirt1/ERK1/2/NF-kappa B signaling pathways

机译:白藜芦醇下调内皮素B型受体在血管平滑肌细胞中通过SIRT1 / ERK1 / 2 / NF-Kappa B信号通路

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摘要

Silent information regulator family protein 1 (Sirt1) has gained attention for protective effects against cardiovasc diseases. Vascular smooth muscle endothelin type B (ETB) receptors are related to the pathogenesis of cardiovascular diseases. Elevated oxidized low-density lipoprotein (ox-LDL) is associated with atherosclerosis. This study will investigate whether resveratrol (a Sirt1 activator, Res) is involved in oxidized low density lipoprotein (ox-LDL)-mediated- regulation of ET(B )receptors in rat superior mesenteric arteries (SMA). The rat SMA segments were cultured in the presence and absence of ox-LDL with or without Res and specific inhibitor (U0126) for the extracellular signal-regulated protein kinase 1 and 2 (ERK1/2) for 24 h. After organ culture, the contractile responses to sarafotoxin 6c (S6c) were studied using a sensitive myograph, and the ET(B )receptor protein expression was detected using Western blotting. The results showed that Res concentration-dependently suppressed the ox-LDL -induced up-regulation of ETB receptors expression and receptor-mediated vasoconstriction. In addition, these effects could be inhibited by U0126. Furthermore, activity of ERK1/2 phosphorylation and P65 acetylation induced by ox-LDL were blocked by Res. In conclusion, Res down-regulated ET(B )receptors through up-regulating Sirtl and followed by ERK1/2/NF-kappa B signaling pathways in the organ culture SMA.
机译:无声信息调节器家庭蛋白1(SIRT1)已经注意到对心脏病毒疾病的保护作用。血管平滑肌内皮素B(ETB)受体与心血管疾病的发病机制有关。升高的氧化低密度脂蛋白(OX-LDL)与动脉粥样硬化有关。该研究将研究白藜芦醇(SIRT1活化剂,RES)是否参与氧化的低密度脂蛋白(OX-LDL) - 在大鼠优质肠系膜(SMA)中的ET(B)受体的调节。对于细胞外信号调节的蛋白激酶1和2(ERK1 / 2),在具有或不具有res和特异性抑制剂(U0126)的情况下在存在和没有res和特异性抑制剂(U0126)的情况下培养大鼠SMA段。在器官培养后,使用敏感的鉴定性研究对SarafoToxin 6C(S6C)的收缩响应,并且使用Western印迹检测Et(B)受体蛋白表达。结果表明,res浓度依赖性抑制了OX-LDL-诱导ETB受体表达和受体介导的血管收缩的上调。此外,U0126可以抑制这些效果。此外,通过RES阻断ERK1 / 2磷酸化和由OX-LDL诱导的p65乙酰化的活性。总之,通过调节SIRTL,res下调的等(b)受体,然后在器官培养SMA中进行ERK1 / 2 / NF-Kappa B信号传导途径。

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