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从……中纯化得到的NMCP-2多糖通过减少心肌细胞凋亡和心肌氧化应激,有效预防阿霉素诱导的心脏毒性。 (你提供的原文中“from”后面缺少具体来源信息)

NMCP-2 polysaccharide purified from effectively prevents doxorubicin-induced cardiotoxicity by decreasing cardiomyocyte apoptosis and myocardial oxidative stress.

作者信息

Xu Na, Lu Yi, Yao Xinmiao, Zhao Rui, Li Zhebin, Li Jialei, Zhang Yinglei, Li Bo, Zhou Ye, Shen Huifang, Wang Liqun, Chen Kaixin, Yang Li, Lu Shuwen

机构信息

Institute of Food Processing Heilongjiang Academy of Agricultural Sciences Harbin China.

Key Laboratory of Zoonosis Research Ministry of Education Institute of Zoonosis College of Veterinary Medicine Jilin University Changchun China.

出版信息

Food Sci Nutr. 2021 Sep 15;9(11):6262-6273. doi: 10.1002/fsn3.2586. eCollection 2021 Nov.

Abstract

Doxorubicin (DOX) is an anthracycline antibiotic used in the clinical treatment of cancer, but its use is limited due to its cardiotoxic effects. Therefore, it is necessary to explore natural compounds that are effective in protecting against the cardiotoxicity caused by DOX. Neutral polysaccharides-2 (NMCP-2) is a natural polysaccharide with antioxidant activity that was isolated and purified from in our laboratory's previous study. This study aimed to investigate the possible protective effect of NMCP-2 on DOX-induced cardiotoxicity and the potential underlying mechanisms. The model of DOX-induced H9C2 cells and the model of DOX-induced mice were used in this study. In in vitro studies of H9C2 myocardial cells, NMCP-2 effectively increased the activity of H9C2 cells, reducing the levels of lactate dehydrogenase (LDH). In the mouse model of DOX-induced chronic cardiotoxicity, NMCP-2 significantly reduced the cardiac index, reduced the release of serum cardiac enzymes, and improved the pathology of murine myocardial tissues, thereby alleviating DOX-induced cardiotoxicity. Further mechanism studies showed that pretreatment with NMCP-2 counteracted the oxidative stress induced by DOX, as indicated by increasing superoxide dismutase (SOD), catalase (CAT), glutathione (GSH) activities, and malondialdehyde (MDA) production decreased. In addition, we observed NMCP-2 inhibited the activation of the mitochondrial apoptosis pathway and regulated the disordered expression of Bcl-2 and Bax in the myocardial tissues of DOX-treated mice. These findings indicated that NMCP-2, a natural bioactive compound, could potentially be used as a food supplement to reduce the cardiotoxicity caused by DOX.

摘要

阿霉素(DOX)是一种用于癌症临床治疗的蒽环类抗生素,但其使用因心脏毒性作用而受到限制。因此,有必要探索对DOX引起的心脏毒性具有保护作用的天然化合物。中性多糖-2(NMCP-2)是一种具有抗氧化活性的天然多糖,是在我们实验室先前的研究中分离纯化得到的。本研究旨在探讨NMCP-2对DOX诱导的心脏毒性可能的保护作用及其潜在的作用机制。本研究使用了DOX诱导的H9C2细胞模型和DOX诱导的小鼠模型。在H9C2心肌细胞的体外研究中,NMCP-2有效提高了H9C2细胞的活性,降低了乳酸脱氢酶(LDH)水平。在DOX诱导的慢性心脏毒性小鼠模型中,NMCP-2显著降低心脏指数,减少血清心脏酶的释放,并改善小鼠心肌组织的病理学,从而减轻DOX诱导的心脏毒性。进一步的机制研究表明,NMCP-2预处理可抵消DOX诱导的氧化应激,表现为超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽(GSH)活性增加,丙二醛(MDA)生成减少。此外,我们观察到NMCP-2抑制了线粒体凋亡途径的激活,并调节了DOX处理小鼠心肌组织中Bcl-2和Bax的紊乱表达。这些发现表明,NMCP-2作为一种天然生物活性化合物,有可能用作食品补充剂以降低DOX引起的心脏毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de48/8565241/b2c713bdeab2/FSN3-9-6262-g001.jpg

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