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自发性高血压大鼠(SHR/NHsd)右心室肥厚与肺内皮素系统的个体间差异有关。

Right Ventricular Hypertrophy in Spontaneously Hypertensive Rats (SHR/NHsd) Is Associated with Inter-Individual Variations of the Pulmonary Endothelin System.

作者信息

Langer Alicia, Schreckenberg Rolf, Schlüter Klaus-Dieter

机构信息

Physiologisches Institut, Justus-Liebig University, Aulweg 129, D-35392 Giessen, Germany.

出版信息

Biology (Basel). 2024 Sep 24;13(10):752. doi: 10.3390/biology13100752.

Abstract

Spontaneously hypertensive rats (SHRs) develop severe hypertension and subsequently left ventricular hypertrophy. Whether they also develop right ventricular hypertrophy is not clear. We analyzed 76 female SHRs (strain SHR/NHsd) and observed severe right ventricular hypertrophy in 7% of these rats (SHR-RVH). Right ventricular hypertrophy did not correlate with the age of the rats and was already seen in one rat at the pre-hypertensive state. The current study investigated the molecular fingerprint of the lung and right ventricle from SHR-RVH and compared this first to SHRs that did develop left but not right ventricular hypertrophy, and second to normotensive rats without hypertrophy. Rats with right ventricular hypertrophy had a decreased expression of the endothelin-B receptor () in the lung, together with an increased protein content of endothelin-1 and an increased expression of . Furthermore, in the right ventricle, a down-regulation of the endothelin-A receptor () was found, consistent with a mild phenotype. The data suggest that in a sub-group of SHR/NHsd rats, low expression of the endothelin clearance receptor (endothelin-B receptor) in the lung triggers an increase in vascular resistance to the right ventricle that then triggers hypertrophy. Our study is the first description of a genetic variant in a defined SHR strain.

摘要

自发性高血压大鼠(SHRs)会发展为严重高血压,随后出现左心室肥厚。它们是否也会出现右心室肥厚尚不清楚。我们分析了76只雌性SHRs(SHR/NHsd品系),发现其中7%的大鼠(SHR-RVH)出现了严重的右心室肥厚。右心室肥厚与大鼠年龄无关,在一只处于高血压前期的大鼠中就已观察到。本研究调查了SHR-RVH大鼠肺和右心室的分子特征,并首先将其与仅出现左心室肥厚而无右心室肥厚的SHRs进行比较,其次与无肥厚的正常血压大鼠进行比较。右心室肥厚的大鼠肺中内皮素B受体()表达降低,同时内皮素-1蛋白含量增加且表达升高。此外,在右心室中发现内皮素A受体()下调,这与轻度表型一致。数据表明,在SHR/NHsd大鼠的一个亚组中,肺中内皮素清除受体(内皮素B受体)的低表达引发了右心室血管阻力增加,进而引发肥厚。我们的研究首次描述了一个特定SHR品系中的基因变异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/088c/11505455/82b9d1dde639/biology-13-00752-g001.jpg

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