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黄芪甲苷IV通过增强Nrf2信号通路抑制阿霉素诱导的心脏铁死亡。

Astragaloside IV inhibits adriamycin-induced cardiac ferroptosis by enhancing Nrf2 signaling.

作者信息

Luo Li-Fei, Guan Peng, Qin Lu-Yun, Wang Jian-Xin, Wang Na, Ji En-Sheng

机构信息

Department of Physiology, Hebei University of Chinese Medicine, Shijiazhuang, Hebei, China.

College of Life Science, Hebei Normal University, Shijiazhuang, Hebei, China.

出版信息

Mol Cell Biochem. 2021 Jul;476(7):2603-2611. doi: 10.1007/s11010-021-04112-6. Epub 2021 Mar 3.

Abstract

Astragaloside IV (AsIV), an active ingredient isolated from traditional Chinese medicine astragalus membranaceus, is beneficial to cardiovascular health. This study aimed to characterize the functional role of AsIV against adriamycin (ADR)-induced cardiomyopathy. Here, healthy rats were treated with ADR and/or AsIV for 35 days. We found that AsIV protected the rats against ADR-induced cardiomyopathy characterized by myocardial fibrosis and cardiac dysfunction. Meanwhile, ADR increased type I and III collagens, TGF-β, NOX2, and NOX4 expression and SMAD2/3 activity in the left ventricles of rats, while those effects were countered by AsIV through suppressing oxidative stress. Moreover, ADR was found to promote cardiac ferroptosis, whereas administration of AsIV attenuated the process via activating Nrf2 signaling pathway and the subsequent GPx4 expression increasing. These results suggest that AsIV might play a protective role against ADR-induced myocardial fibrosis, which may partly attribute to its anti-ferroptotic action by enhancing Nrf2 signaling.

摘要

黄芪甲苷(AsIV)是从传统中药黄芪中分离出的一种活性成分,对心血管健康有益。本研究旨在表征AsIV对阿霉素(ADR)诱导的心肌病的功能作用。在此,将健康大鼠用ADR和/或AsIV处理35天。我们发现AsIV保护大鼠免受ADR诱导的以心肌纤维化和心脏功能障碍为特征的心肌病的影响。同时,ADR增加了大鼠左心室中I型和III型胶原蛋白、转化生长因子-β、Nox2和Nox4的表达以及SMAD2/3的活性,而AsIV通过抑制氧化应激来对抗这些影响。此外,发现ADR会促进心脏铁死亡,而给予AsIV则通过激活Nrf2信号通路和随后增加GPx4表达来减轻这一过程。这些结果表明,AsIV可能对ADR诱导的心肌纤维化起保护作用,这可能部分归因于其通过增强Nrf2信号传导的抗铁死亡作用。

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