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运动诱导的2肾1夹型高血压大鼠股静脉中血管紧张素II反应的调节

Exercise-Induced Modulation of Angiotensin II Responses in Femoral Veins From 2-Kidney-1-Clip Hypertensive Rats.

作者信息

Chies Agnaldo Bruno, Spadella Maria Angélica, de Oliveira Priscila Ramos, Domeniconi Raquel Fantin, de Mello Santos Talita, Moreira Roseli Peres, Rosales Carla B, Casarini Dulce Elena, Navar Luis Gabriel

机构信息

Laboratory of Pharmacology, Marília Medical School, Marília, Brazil.

Human Embryology Laboratory, Marília Medical School, Marília, Brazil.

出版信息

Front Physiol. 2021 Apr 7;12:620438. doi: 10.3389/fphys.2021.620438. eCollection 2021.

Abstract

The present study investigated the angiotensin II (Ang II) responses in rat femoral veins taken from 2-kidney-1clip (2K1C) hypertensive rats at 4 weeks after clipping, as well as the effects of exercise on these responses. In this manner, femoral veins taken from 2K1C rats kept at rest or exposed to acute exercise or to exercise training were challenged with Ang II or endothelin-1 (ET-1) in organ bath. Simultaneously, the presence of cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) were determined in these preparations by western blotting. In these experiments, femoral veins exhibited subdued Ang II responses. However, after nitric oxide (NO) synthesis blockade, the responses were higher in the femoral veins taken from animals kept at rest [0.137(0.049-0.245); = 10] than those obtained in trained animals kept at rest [0.008(0.001-0.041); = 10] or studied after a single bout of exercise [0.001(0.001-0.054); = 11]. In preparations in which, in addition to NO synthesis, both the local production of prostanoids and the action of ET-1 on type A (ET) or B (ET) receptors were inhibited, the differences induced by exercise were no longer observed. In addition, neither ET-1 responses nor the presence of COX-1 and COX-2 in these preparations were modified by the employed exercise protocols. In conclusion, NO maintains Ang II responses reduced in femoral veins of 2K1C animals at rest. However, vasodilator prostanoids as well as other relaxing mechanisms, activated by ET stimulation, are mobilized by exercise to cooperate with NO in order to maintain controlled Ang II responses in femoral veins.

摘要

本研究调查了夹闭4周后的二肾一夹(2K1C)高血压大鼠股静脉中血管紧张素II(Ang II)的反应,以及运动对这些反应的影响。采用这种方式,将取自静息状态、急性运动或运动训练后的2K1C大鼠的股静脉,在器官浴中用Ang II或内皮素-1(ET-1)进行刺激。同时,通过蛋白质免疫印迹法测定这些标本中环氧化酶-1(COX-1)和环氧化酶-2(COX-2)的存在情况。在这些实验中,股静脉对Ang II的反应减弱。然而,一氧化氮(NO)合成被阻断后,取自静息动物的股静脉反应[0.137(0.049 - 0.245); n = 10]高于取自静息训练动物的股静脉反应[0.008(0.001 - 0.041); n = 10]或单次运动后检测的股静脉反应[0.001(0.001 - 0.054); n = 11]。在除了NO合成外,前列腺素的局部产生以及ET-1对A型(ET)或B型(ET)受体的作用均被抑制的标本中,不再观察到运动引起的差异。此外,所采用的运动方案并未改变这些标本中ET-1的反应以及COX-1和COX-2的存在情况。总之,NO维持了2K1C动物静息时股静脉中降低的Ang II反应。然而,运动可动员由ET刺激激活的血管舒张性前列腺素以及其他舒张机制,与NO协同作用,以维持股静脉中Ang II反应的可控性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d355/8058411/970699effa16/fphys-12-620438-g001.jpg

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