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在肝硬化和门静脉高压症患者中,尿皮质素 II 和 GPR14 的表达增加。

Increased expression of urotensin II and GPR14 in patients with cirrhosis and portal hypertension.

机构信息

Department of General Surgery, Xuan Wu Hospital, Capital Medical University, Beijing 100050, P.R. China.

出版信息

Int J Mol Med. 2010 Jun;25(6):845-51. doi: 10.3892/ijmm_00000413.

Abstract

Urotensin II (UII) and its receptor (UT or GPR14) are involved in liver fibrosis and portal hypertension. Nevertheless, expression of the UII/UT system in the liver of patients with portal hypertension has not been elucidated. UII and UT gene expression were quantified in liver biopsy samples from patients with hepatitis-B-virus-associated cirrhosis and portal hypertension, and from normal controls by using quantitative real-time PCR. The liver distribution of UT was determined by means of immunohistochemistry and immunofluorescence. Western blot analysis was used to assess liver levels of UT. Simultaneously, we measured intra-operative free portal venous pressure (FPVP) and collected plasma for UII measurement by ELISA. UT expression at the mRNA and protein level was enhanced significantly in the liver of patients with cirrhosis and portal hypertension, compared with that in healthy controls. UT protein expression was concentrated mainly in the Kupffer cells and sinusoidal endothelial cells. In cirrhotic tissue, UII gene expression was increased 5-fold in comparison to that in normal liver tissue. Plasma UII level was higher in cirrhotic patients compared with controls and was correlated with FPVP (r=0.807; P<0.001) and UII mRNA in the liver (r=0.802; P<0.001). These findings suggest that the intrahepatic UII/UT system has an important pathophysiological role in cirrhosis and portal hypertension.

摘要

尾加压素 II(UII)及其受体(UT 或 GPR14)参与肝纤维化和门静脉高压。然而,门静脉高压患者肝脏中 UII/UT 系统的表达尚未阐明。通过定量实时 PCR 定量检测乙型肝炎病毒相关肝硬化和门静脉高压患者及正常对照者肝活检样本中的 UII 和 UT 基因表达。通过免疫组织化学和免疫荧光法确定 UT 在肝脏中的分布。Western blot 分析用于评估 UT 在肝脏中的水平。同时,我们测量术中自由门静脉压力(FPVP)并通过 ELISA 测量血浆中的 UII。与健康对照组相比,肝硬化和门静脉高压患者肝脏中 UT 的 mRNA 和蛋白水平表达显著增强。UT 蛋白表达主要集中在枯否细胞和窦内皮细胞中。与正常肝组织相比,肝硬化组织中 UII 基因表达增加了 5 倍。与对照组相比,肝硬化患者的血浆 UII 水平较高,且与 FPVP(r=0.807;P<0.001)和肝脏中的 UII mRNA(r=0.802;P<0.001)相关。这些发现表明,肝内 UII/UT 系统在肝硬化和门静脉高压中具有重要的病理生理作用。

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