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黄芪甲苷通过抑制 NADPH 氧化酶来源的氧化应激缓解阿霉素诱导的心肌病。

Astragaloside IV alleviates doxorubicin induced cardiomyopathy by inhibiting NADPH oxidase derived oxidative stress.

机构信息

Department of Internal Medicine-Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, 250117, China.

Department of Traditional Chinese Medicine, Shandong Academy of Occupational Health and Occupational Medicine, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, 250001, China.

出版信息

Eur J Pharmacol. 2019 Sep 15;859:172490. doi: 10.1016/j.ejphar.2019.172490. Epub 2019 Jun 21.

Abstract

Doxorubicin (DOX) is a classic anti-tumor chemotherapeutic used to treat a wide range of tumors. One major downfall of DOX treatment is it can induce fatal cardiotoxicity. Astragaloside IV (AS-IV) is one of the primary active ingredients that can be isolated from the traditional Chinese herbal medicine, Astragalus membranaceus. This study uses both in vitro and in vivo tools to investigate whether AS-IV alleviates DOX induced cardiomyopathy. We found that AS-IV supplementation alleviates body weight loss, myocardial injury, apoptosis of cardiomyocytes, cardiac fibrosis and cardiac dysfunction in DOX-treated mice. Also, DOX-induced cardiomyocyte injury and apoptosis were effectively improved by AS-IV treatment in vitro. NADPH oxidase (NOX) plays an important role in the progress of the oxidative signal transduction and DOX-induced cardiomyopathy. In this study, we found that AS-IV treatment relieves DOX-induced NOX2 and NOX4 expression and oxidative stress in cardiomyocytes. In conclusion, AS-IV, an antioxidant, attenuates DOX-induced cardiomyopathy through the suppression of NOX2 and NOX4.

摘要

阿霉素(DOX)是一种经典的抗肿瘤化疗药物,用于治疗多种肿瘤。DOX 治疗的一个主要缺点是它会引起致命的心脏毒性。黄芪甲苷(AS-IV)是从传统中药黄芪中分离得到的主要活性成分之一。本研究使用体外和体内工具来研究 AS-IV 是否缓解 DOX 诱导的心肌病。我们发现,AS-IV 补充可减轻 DOX 处理的小鼠体重减轻、心肌损伤、心肌细胞凋亡、心脏纤维化和心功能障碍。此外,AS-IV 处理在体外有效改善了 DOX 诱导的心肌细胞损伤和凋亡。NADPH 氧化酶(NOX)在氧化信号转导和 DOX 诱导的心肌病的进展中起重要作用。在这项研究中,我们发现 AS-IV 处理可减轻 DOX 诱导的心肌细胞中 NOX2 和 NOX4 的表达和氧化应激。总之,抗氧化剂 AS-IV 通过抑制 NOX2 和 NOX4 减轻 DOX 诱导的心肌病。

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