首页> 外文期刊>Hypertension research: Official journal of the Japanese Society of Hypertension >Comparison of 12-lipoxygenase expression in vascular smooth muscle cells from old normotensive Wistar-Kyoto rats with spontaneously hypertensive rats
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Comparison of 12-lipoxygenase expression in vascular smooth muscle cells from old normotensive Wistar-Kyoto rats with spontaneously hypertensive rats

机译:老血压正常Wistar-Kyoto大鼠与自发性高血压大鼠血管平滑肌细胞中12-脂氧合酶表达的比较

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摘要

Vascular aging and essential hypertension cause similar structural and molecular modifications in the vasculature. The 12-lipoxygenase (LO) pathway of arachidonic acid metabolism is linked to cell growth and the pathology of hypertension. Thus, elevated expression of 12-LO has been observed in vascular smooth muscle cells (VSMCs) from spontaneously hypertensive rats (SHR). In the present study, we investigated the differences in 12-LO expression and activity between VSMCs from old normotensive Wistar-Kyoto rats (old WKY, 90-week old) and SHR (13-week old). The protein and mRNA expression of basal or angiotensin II (Ang ID-induced 12-LO in old WKY VSMCs were higher than those in SHR VSMCs. The degradation rate of 12-LO mRNA in old WKY VSMCs was slower than that in SHR VSMCs. However, basal or Ang 11-induced 12-LO mRNAs in both old WKY and SHR VSMCs decayed more rapidly than that in young WKY (13-week old) VSMCs. Higher expression of 12-LO in old WKY VSMCs than in SHR VSMCs was correlated with the expression level of Ang II subtype 1 receptor (AT_1R). The reduced levels of nitric oxide (NO) in old WKY and SHR VSMCs compared with young WKY VSMCs were similar, and there was no significant difference in NO production between old WKY and SHR VSMCs transfected with 12-LO siRNA. In addition, in contrast to the proliferation of SHR VSMCs, the proliferation of old WKY VSMCs was not dependent on 12-LO activation. These results suggest that the potential role of 12-LO in normotensive aging vasculature may be different from that in SHR vasculature.
机译:血管老化和原发性高血压在血管系统中引起相似的结构和分子修饰。花生四烯酸代谢的12-脂氧合酶(LO)途径与细胞生长和高血压的病理状况有关。因此,已经观察到自发性高血压大鼠(SHR)的血管平滑肌细胞(VSMC)中12-LO的表达升高。在本研究中,我们调查了老的正常血压Wistar-Kyoto大鼠(老的WKY,90周龄)和SHR(13周的老龄大鼠)的VSMC之间12-LO表达和活性的差异。 WKY VSMC中基底或血管紧张素Ⅱ(Ang ID诱导的12-LO)的蛋白和mRNA表达高于SHR VSMC中的12-LO mRNA降解速度,SID VSMC中12-LO mRNA的降解速度较SHR VSMC慢。然而,老的WKY和SHR VSMCs中基础或Ang 11诱导的12-LO mRNA的衰减比年轻的WKY(13周龄)VSMCs衰减更快,老的WKY VSMC中12-LO的表达高于SHR VSMCs。与Ang II亚型1受体(AT_1R)的表达水平相关,老WKY和SHR VSMC中一氧化氮(NO)的降低水平与年轻WKY VSMCs相似,并且老WKY之间NO生成量无显着差异和SHR VSMCs转染了12-LO siRNA。此外,与SHR VSMCs的增殖相反,旧的WKY VSMCs的增殖不依赖于12-LO激活,这些结果表明12-LO在降血压中的潜在作用老化的脉管系统可能与SHR脉管系统不同。

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