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糖尿病期间,内皮型一氧化氮合酶增加导致肾小动脉中连接蛋白表达的变化。

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

作者信息

Zhang Jian Hong, Kawashima Seinosuke, Yokoyama Mitsuhiro, Huang Paul, Hill Caryl E

机构信息

Division of Neuroscience, John Curtin School of Medical Research, Australian National University, Canberra, ACT 2602, Australia.

出版信息

Anat Rec A Discov Mol Cell Evol Biol. 2006 Sep;288(9):1000-8. doi: 10.1002/ar.a.20369.

Abstract

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.

摘要

先前的研究表明,与肾小球后血管相比,连接蛋白(Cx)在肾小球前血管中的表达要高得多,并且在糖尿病期间这些差异会更加明显。由于有报道称一氧化氮(NO)可改变内皮细胞和肌肉细胞中的Cx表达,且糖尿病时NO的生物利用度会发生改变,因此我们推测NO可能是糖尿病期间这些变化的原因。使用免疫组织化学方法在eNOS表达上调(eNOS转基因)或下调(eNOS基因敲除)的小鼠中研究Cx表达。通过腹腔注射单剂量的四氧嘧啶或多次低剂量的链脲佐菌素诱导糖尿病。在eNOS转基因小鼠中,传入小动脉平滑肌细胞中Cx40的表达增加,而传出小动脉内皮细胞中Cx43的表达缺失,这与野生型小鼠在糖尿病期间发生的变化相似。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基因敲除小鼠中诱导糖尿病未能使传入或传出小动脉中的Cx40或Cx43产生任何变化。免疫组织化学显示,野生型糖尿病小鼠和eNOS转基因小鼠肾小动脉内皮中的eNOS表达增加,但eNOS基因敲除小鼠的小动脉中不存在这种情况。我们得出结论,糖尿病期间传入和传出小动脉中Cx表达的变化可能是由于eNOS增加所致。

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