首页> 外文期刊>Hepatology research: the official journal of the Japan Society of Hepatology >Decreased renal expressions of heat shock protein-72 and -25 are associated with renal dysfunction in biliary cirrhotic rats.
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Decreased renal expressions of heat shock protein-72 and -25 are associated with renal dysfunction in biliary cirrhotic rats.

机译:胆汁性肝硬化大鼠肾组织中热休克蛋白72和-25的表达降低与肾功能不全有关。

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摘要

During the course of liver cirrhosis, severe renal complications frequently occur. However, the pathogenesis of renal dysfunction in liver cirrhosis has not been completely understood. In this study, we investigated the association between renal function and expressions of renal heat shock proteins (HSPs) in biliary cirrhotic rats. Following bile duct ligation (BDL), renal function and expressions of HSPs were compared in control and BDL cirrhotic rats. Serum BUN and creatinine levels were significantly higher in cirrhotic rats compared with control rats at 4 weeks post-BDL operation. Renal expressions of HSP72 and HSP25 were decreased with progression of liver cirrhosis in BDL rats by Western blotting. Immunohistochemistry revealed that expression of renal HSP72 was suppressed in tubular epithelial cells, and expression of renal HSP25 was suppressed not only in tubular epithelial cells but also in blood vessels in rats with liver cirrhosis. Renal expressions of HSP90 and HSP60 did not differ between control and BDL rats. Renal function was impaired in biliary cirrhotic rats with decreased expressions of renal HSP72 and HSP25. These findings suggest that decreased expressions of renal HSP72 and HSP25 may be a part of the pathogenesis of renal dysfunction in liver cirrhosis.
机译:在肝硬化过程中,经常发生严重的肾脏并发症。但是,肝硬化中肾功能不全的发病机理尚未完全了解。在这项研究中,我们调查了胆汁性肝硬化大鼠肾功能与肾热休克蛋白(HSPs)表达之间的关系。胆管结扎(BDL)后,比较对照组和BDL肝硬化大鼠的肾功能和HSPs表达。 BDL术后4周,肝硬化大鼠的血清BUN和肌酐水平明显高于对照组。 Western Blotting法检测BDL大鼠肝组织中HSP72和HSP25的肾表达降低。免疫组织化学显示,肝硬化大鼠肾小管上皮细胞中肾HSP72的表达受到抑制,不仅肾小管上皮细胞中肾HSP25的表达受到抑制,肝硬化大鼠血管中HSP25的表达也受到抑制。在对照和BDL大鼠之间,HSP90和HSP60的肾脏表达没有差异。胆汁性肝硬化大鼠肾脏功能受损,肾脏HSP72和HSP25表达降低。这些发现表明,肾HSP72和HSP25表达降低可能是肝硬化肾功能不全的发病机制的一部分。

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