肥胖wistar大鼠肾脏循环内皮素(ET)-1和内皮素受体(ETA、ETB)表达的升高。

International journal of physiology, pathophysiology and pharmacology Pub Date : 2019-04-15 eCollection Date: 2019-01-01
Irfan Idris, Andi Wardihan Sinrang, Aryadi Arsyad, Syafrudin Alwi, Muhammad Isman Sandira
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引用次数: 0

摘要

背景:据报道,内皮素(ET)-1 是一种循环蛋白,其在不同器官中的受体(ETA 和 ETB)在包括肥胖症在内的多种疾病中起着关键作用。然而,有关肥胖症患者心室和肾脏中 ETA 和 ETB 表达变化的报道较少。本研究旨在观察与非肥胖 Wistar 大鼠相比,肥胖大鼠心室和肾脏中循环 ET-1 的水平以及 ETA/ETB 的表达:方法:将 14 周和 34 周肥胖 Wistar 大鼠组与年龄相仿的非肥胖对照组进行比较。肥胖组采用高热量蛋白质饮食 CP 551 + 奶粉,对照组采用标准热量蛋白质饮食 AD II。两组分别在第14周和第24周终止实验后,采用酶联免疫吸附试验(ELISA)技术测定心室和肾脏循环中ET-1、ETA和ETB的浓度:结果:肥胖大鼠循环中 ET-1 的水平、肾脏中 ETA 和 ETB 的表达以及低密度脂蛋白均显著高于对照组(T 检验),心室中发现 PA 和 ETB。肥胖组和对照组年轻大鼠循环中的 ET-1、ETA 和 ETB 表达水平无差异(P>0.05)。两组大鼠的高密度脂蛋白水平均低于正常值:结论:老年肥胖大鼠的肥胖会通过 ET-1 和 ETA/ETB 的活性导致肾脏血管失调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The rise of circulatory endothelin (ET)-1 and endothelin receptors (ETA, ETB) expression in kidney of obese wistar rat.

Background: Endothelin (ET)-1, a circulatory protein, and its receptors (ETA and ETB) in various organs were reported to play a pivotal role in many diseases, including obesity. However, the changes of ETA and ETB expression in ventricle and kidney in obesity was less reported. The study is designed to observe the level of circulatory ET-1 and expression of ETA/ETB in ventricle and kidney of obese, as compared to non-obese, Wistar rats.

Methods: Groups of obese 14 and 34 weeks Wistar rats were compared to non-obese controls at similar ages. The obesity status was achieved by feeding the with high calories protein diet CP 551 + milk powder, while the control group was fed with a standard calorie protein AD II diet. The concentration of circulatory ET-1, ETA and ETB of ventricle and kidney were measured by Enzyme Linked Immunosorbent Assay (ELISA) technique after the termination of both groups at 14th and 24th weeks.

Results: The level of circulatory ET-1, expression of ETA and ETB in kidney, and LDL of obese rats were significantly higher than control rats (T-Test, P<0.05) in the elder groups, while no differences of the ETA and ETB were found in the ventricle. No differences of the levels of circulatory ET-1, ETA and ETB expression were found between obese and control groups of younger rats (P>0.05). HDL levels were under normal value for both groups.

Conclusion: Obesity in elder obese rats leads to dysregulation of kidney vessels through activity of ET-1 and ETA/ETB.

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