衰老过程中糖尿病大鼠肾脏结缔组织生长因子表达的变化

Leonora Bedeković, K. Vukojević
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摘要

背景:糖尿病肾病(DN)是世界上最常见的慢性肾功能衰竭的原因。DN的病理机制似乎有不同的发病、血流动力学和代谢过程。我们研究了结缔组织生长因子(CTGF)在糖尿病大鼠肾脏中随时间的表达。方法:雄性sd - dawley大鼠分别注射链脲佐菌素(STZ) 55mg/kg(糖尿病组)和柠檬酸缓冲液(对照组)。在STZ攻击后2周、2个月、6个月和12个月取肾,并将其切成肾小球、近曲小管(PCT)和远曲小管(DCT)三种不同的肾脏结构。免疫组织化学染色检测CTGF的表达。结果:STZ攻药后2周和2个月CTGF表达均有显著差异,糖尿病大鼠CTGF表达较高。糖尿病发病2周后,糖尿病大鼠远端小管中出现高表达的CTGF。糖尿病大鼠肾小球中CTGF的表达在糖尿病诱导后12个月最高,而对照组在整个研究过程中完全没有CTGF的表达。结论:CTGF表达的主要变化发生在糖尿病的前2个月内,尤其是在DTC,这意味着糖尿病肾脏的病理生理变化早发,而这种变化通常会随着年龄的增长而发生。这些发现有助于我们理解与DN相关的变化,并指导潜在的适当治疗方式。关键词:糖尿病,肾病,慢性肾功能衰竭,结缔组织生长因子(CTGF)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in Expression of the Connective Tissue Growth Factor in the Kidneys of Diabetic Rats During Aging
Background: Diabetic nephropathy (DN) is the most common cause of chronic renal failure in the world. There appears to be different pathogenetic, hemodynamic and metabolic processes leading to the pathologic mechanisms in DN. We studied the expression of connective tissue growth factor (CTGF) in the kidneys of diabetic rats over time.Methods: Male Sprague-Dawley rats were injected with 55mg/kg streptozotocin (STZ) (diabetes mellitus (DM) group) or with citrate buffer (control group). The rat kidneys were harvested 2 weeks, 2 months, 6 months and 12 months following the STZ challenge, and sectioned into three different kidney structures: glomeruli, proximal convoluted tubule (PCT) and distal convoluted tubule (DCT). Sections were immunohistochemically stained to monitor the expression of CTGF. Results:Significant differences in CTGF expression were observed 2 weeks and 2 months after the STZ challenge, with higher CTGF expression in diabetic rats. Two weeks post DM onset, high CTGF expression was demonstrated in the distal tubules of the diabetic rats. The expression of CTGF in the glomeruli of diabetic rats washighest 12 months after diabetes induction, with a complete absence of CTGF expression in the control groups throughout the study.Conclusions:The major change in expression of CTGF occurs within the first 2 months of DM, particularly in the DTC, implying an early onset of pathophysiological changes in diabetic kidneys, which would normally occur with aging. These findings help to contribute to our understanding of changes associated with DN and guide towards potentially appropriate treatment modalities.Key words: diabetes mellitus (DM), nephropathy, chronic renal failure, connective tissue growth factor (CTGF)
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