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黄芪(蒙古黄芪)通过下调 ESR1 信号通路 RhoA/ROCK 改善心室重构。

Astragalus (Astragalus mongholicus) Improves Ventricular Remodeling via ESR1 Downregulation RhoA/ROCK Pathway.

机构信息

Department of Cardiology, The Affiliated Hospital of Yunnan University.

School of Medicine, Yunnan University.

出版信息

Int Heart J. 2023 Nov 30;64(6):1148-1156. doi: 10.1536/ihj.23-265. Epub 2023 Nov 14.

Abstract

Astragalus (Astragalus mongholicus) alleviates myocardial remodeling caused by hypertension. However, the detailed molecular mechanism is unclear. This study aims to investigate the effect of Astragalus on ventricular remodeling in ovariectomized spontaneous hypertensive rats (OVX-SHR).Female SHR/NCrl rats were subjected to bilateral ovariectomy to establish the OVX-SHR model and treated with Astragalus extract by gavage. The hemodynamics and cardiac function parameters were measured. HE and Masson staining were used to detect the pathological structure of myocardial remodeling and observe the hyperplasia of myocardial collagen fibers. The immunohistochemistry tested the level of α-SMA. The expression levels of inflammatory cytokines, IκB, p65, Cleaved-Caspase3, RhoA, and ROCK1/2 were detected using Western blot. The method of qRT-PCR measured the expression of matrix metalloproteinase (MMP-2 and MMP-9).Hemodynamic and cardiac function parameters were significantly improved after a high dose of Astragalus extract and Valsartan treatment. The myocardial integrity of the model group was significantly reduced, arranged loosely, and disordered, while the expression of α-SMA was increased. However, Astragalus extract and Valsartan treatments significantly reduced the pathological damage and α-SMA. The levels of TNF-α, IL-1β, IL-6, TGF-β, MMP-2, and MMP-9 in the model group were increased but decreased after Astragalus extract treatment. Adding an ESR1 inhibitor attenuated the improvement effect of Astragalus extract on myocardial remodeling and restored the expression of RhoA and ROCK1/2.Astragalus extract attenuates the cardiac damage in OVX-SHR by downregulating the RhoA/ROCK pathway through ESR1.

摘要

黄芪(蒙古黄芪)可减轻高血压引起的心肌重构。然而,其详细的分子机制尚不清楚。本研究旨在探讨黄芪对去卵巢自发性高血压大鼠(OVX-SHR)心室重构的影响。雌性 SHR/NCrl 大鼠行双侧卵巢切除术建立 OVX-SHR 模型,并给予黄芪提取物灌胃。测量血流动力学和心功能参数。HE 和 Masson 染色用于检测心肌重构的病理结构和观察心肌胶原纤维的增生。免疫组化检测α-SMA 水平。Western blot 检测炎症细胞因子、IκB、p65、Cleaved-Caspase3、RhoA 和 ROCK1/2 的表达水平。qRT-PCR 法检测基质金属蛋白酶(MMP-2 和 MMP-9)的表达。

黄芪提取物高剂量和缬沙坦治疗后,血流动力学和心功能参数明显改善。模型组心肌完整性明显降低,排列松散,紊乱,α-SMA 表达增加。然而,黄芪提取物和缬沙坦治疗明显减轻了病理损伤和α-SMA。模型组 TNF-α、IL-1β、IL-6、TGF-β、MMP-2 和 MMP-9 水平升高,但经黄芪提取物治疗后降低。添加 ESR1 抑制剂减弱了黄芪提取物对心肌重构的改善作用,并恢复了 RhoA 和 ROCK1/2 的表达。

黄芪提取物通过下调 ESR1 介导的 RhoA/ROCK 通路减轻 OVX-SHR 的心脏损伤。

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