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血府逐瘀汤通过抑制自噬保护心肌细胞免受缺氧/复氧损伤。

XuefuZhuyu decoction protected cardiomyocytes against hypoxia/reoxygenation injury by inhibiting autophagy.

作者信息

Shi Xiaowen, Zhu Haiyan, Zhang Yuanyuan, Zhou Mingmei, Tang Danli, Zhang Huamin

机构信息

Center for Chinese Medical Therapy and Systems Biology, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, People's Republic of China.

Department of Microbiological & Biochemical Pharmacy, School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai, 201203, People's Republic of China.

出版信息

BMC Complement Altern Med. 2017 Jun 19;17(1):325. doi: 10.1186/s12906-017-1822-0.

Abstract

BACKGROUND

XuefuZhuyu decoction (XFZY) is a well-known traditional Chinese herbal medicine for the treatment of various cardiovascular diseases, such as unstable angina pectoris and myocardial ischemia-reperfusion injury. However, the mechanism by which XFZY contributes to the amelioration of cardiac injury remains unclear.

METHODS

H9C2 cells were cultured under the hypoxic condition for 10 h and reoxygenated for 2 h. In the presence of various concentrations of XFZY for 12 h, the cell viability was measured by MTT assay. The protective effect of XFZY in hypoxia/reoxygenation (H/R) cell model was confirmed by measuring the amount of LDH released into the extracellular fluid. Cell apoptosis was measured by western blotting. The autophagy level of H9C2 cells and the correlative pathway were determined by transmission electron microscopy, Cyto-ID® Autophagy Detection Kit, and western blotting.

RESULTS

In this study, we investigated the effects of XFZY on H/R induced cardiac injury. The results showed that treatment with XFZY significantly inhibited autophagy induced by H/R, with decreased formation of autophagosomes as well as the expression of LC3-II/LC3-I ratio and Beclin 1 after H/R. Importantly, inhibition of autophagy by XFZY resulted in enhanced cell viability and decreased apoptosis. XFZY also inhibited the activation of AMPK and upregulated the phosphorylation of mammalian target of Rapamycin (mTOR).

CONCLUSIONS

The cardioprotective effects of XFZY during H/R were mediated by inhibiting autophagy via regulating AMPK-mTOR signaling pathways.

摘要

背景

血府逐瘀汤(XFZY)是一种著名的用于治疗各种心血管疾病的传统中药,如不稳定型心绞痛和心肌缺血-再灌注损伤。然而,血府逐瘀汤改善心脏损伤的机制仍不清楚。

方法

将H9C2细胞在缺氧条件下培养10小时,然后复氧2小时。在存在不同浓度血府逐瘀汤的情况下培养12小时,通过MTT法测定细胞活力。通过测量释放到细胞外液中的乳酸脱氢酶(LDH)量,证实血府逐瘀汤在缺氧/复氧(H/R)细胞模型中的保护作用。通过蛋白质印迹法检测细胞凋亡。通过透射电子显微镜、Cyto-ID®自噬检测试剂盒和蛋白质印迹法测定H9C2细胞的自噬水平及相关通路。

结果

在本研究中,我们研究了血府逐瘀汤对H/R诱导的心脏损伤的影响。结果表明,血府逐瘀汤治疗显著抑制了H/R诱导的自噬,H/R后自噬体形成减少,LC3-II/LC3-I比值和Beclin 1的表达降低。重要的是,血府逐瘀汤抑制自噬导致细胞活力增强和凋亡减少。血府逐瘀汤还抑制了AMPK的激活,并上调了雷帕霉素靶蛋白(mTOR)的磷酸化。

结论

血府逐瘀汤在H/R期间的心脏保护作用是通过调节AMPK-mTOR信号通路抑制自噬来介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b898/5477241/5b0c589e4def/12906_2017_1822_Fig1_HTML.jpg

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