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Increased eNOS accounts for changes in connexin expression in renal arterioles during diabetes

机译:eNOS升高解释了糖尿病期间肾小动脉连接蛋白表达的变化

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Previous studies have shown that connexin (Cx) expression is considerably higher in the preglomerular compared to postglomerular vasculature and that these differences are accentuated during diabetes. Since nitric oxide (NO) has been reported to alter Cx expression in endothelial cells and muscle cells and NO bioavailability is altered in diabetes, we hypothesized that NO may be responsible for the changes during diabetes. Cx expression was studied using immunohistochemistry in mice in which eNOS expression was either upregulated (eNOS transgenic) or downregulated (eNOS knockout). Diabetes was induced intraperitoneally with a single dose of alloxan or multiple low doses of streptozotocin. Expression of Cx40 in smooth muscle cells of afferent arterioles was increased, while expression of Cx43 in endothelial cells of efferent arterioles was absent in eNOS transgenic mice, similar to the changes occurring in wild-type mice during diabetes. Expression of Cx40 and Cx43 in eNOS knockout mice was not different from control; however, induction of diabetes in eNOS knockout mice failed to produce any changes in Cx40 or Cx43 in either afferent or efferent arterioles. Immunohistochemistry showed that eNOS expression was increased in the endothelium of renal arterioles in wild-type diabetic and eNOS transgenic mice, but absent from arterioles of eNOS knockout mice. We conclude that changes occurring in Cx expression in afferent and efferent arterioles during diabetes may result from increased eNOS.
机译:先前的研究表明,与肾小球后的脉管系统相比,连接蛋白(Cx)的表达在肾小球前明显更高,并且这些差异在糖尿病期间更加明显。由于已经报道一氧化氮(NO)会改变内皮细胞和肌肉细胞中Cx的表达,并且在糖尿病中NO的生物利用度也会发生变化,因此我们假设NO可能是糖尿病期间这种变化的原因。使用免疫组织化学在小鼠中研究了Cx表达,其中eNOS表达被上调(eNOS转基因)或被下调(eNOS敲除)。用单剂量的四氧嘧啶或多次低剂量的链脲佐菌素腹膜内诱导糖尿病。在eNOS转基因小鼠中,传入小动脉的平滑肌细胞中Cx40的表达增加,而传出小动脉的内皮细胞中Cx43的表达缺失,这与糖尿病期间野生型小鼠的变化相似。 eNOS基因敲除小鼠中Cx40和Cx43的表达与对照组无差异;然而,在eNOS基因敲除小鼠中诱发糖尿病未能使传入或传出的小动脉Cx40或Cx43产生任何变化。免疫组织化学表明,在野生型糖尿病和eNOS转基因小鼠中,肾小动脉内皮中eNOS表达增加,而敲除eNOS小鼠的小动脉中则没有。我们得出结论,糖尿病期间传入和传出的小动脉Cx表达发生的变化可能是由于eNOS增加所致。

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