首页> 外文期刊>Diabetes/metabolism research and reviews >Proinsulin C-peptide abrogates type-1 diabetes-induced increase of renal endothelial nitric oxide synthase in rats.
【24h】

Proinsulin C-peptide abrogates type-1 diabetes-induced increase of renal endothelial nitric oxide synthase in rats.

机译:胰岛素原C肽消除了1型糖尿病引起的大鼠肾内皮一氧化氮合酶的增加。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: Proinsulin C-peptide shows ameliorative effects on diabetic complications, possibly through the production of nitric oxide (NO). On the contrary, increased local availability of NO and expression of endothelial NO synthase (eNOS) in the renal endothelium are shown to be involved in the progression of diabetic nephropathy. The aim of this study was to elucidate the effect of C-peptide and insulin as a reference on the eNOS expression in the early phase of type 1 diabetic rat kidney. METHODS: Type 1 diabetes in rats was produced by streptozotocin injection and some of the rats were treated with either C-peptide or insulin by the aid of an osmotic pump for 1 week. Conventional biochemical and histological analyses were performed on tissue samples. RESULTS: The diabetic rats showed hyperglycemia with over 90% reduction of endogenous insulin and C-peptide. Replacement with C-peptide or insulin resulted in recovery of weight lost, but only insulin infusion lowered plasma-glucose concentration. The eNOS protein was localized in glomeruli and endothelial cells of arterioles, and its amounts in the kidneys, but not in the lungs, of diabetic rats was increased. Replacement with C-peptide or insulin-abrogated diabetes-induced increase of renal eNOS protein. CONCLUSION: The results indicate that C-peptide suppresses diabetes-induced abnormal renal eNOS expression, by which C-peptide may exert beneficial effects on diabetic nephropathy. Copyright (c) 2007 John Wiley & Sons, Ltd.
机译:背景:胰岛素原C肽可能通过产生一氧化氮(NO)改善糖尿病并发症。相反,在糖尿病性肾病的发展中,增加了NO的局部可利用性和在肾内皮中的内皮NO合酶(eNOS)的表达。这项研究的目的是阐明C肽和胰岛素对1型糖尿病大鼠肾脏早期eNOS表达的影响。方法:通过链脲佐菌素注射产生大鼠1型糖尿病,并在部分C肽或胰岛素的帮助下,通过渗透泵对大鼠进行1周的治疗。对组织样品进行常规的生化和组织学分析。结果:糖尿病大鼠表现出高血糖,内源性胰岛素和C肽减少90%以上。用C肽或胰岛素替代可导致体重减轻,但仅输注胰岛素可降低血浆葡萄糖浓度。 eNOS蛋白位于小动脉的肾小球和内皮细胞中,并且在糖尿病大鼠的肾脏而不是肺中的含量增加。用C肽或胰岛素减轻的糖尿病替代引起的肾eNOS蛋白增加。结论:C肽可抑制糖尿病引起的肾脏异常肾脏eNOS表达,从而可能对糖尿病肾病产生有益的作用。版权所有(c)2007 John Wiley&Sons,Ltd.

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号