Aconitine attenuates mitochondrial dysfunction of cardiomyocytes via promoting deacetylation of cyclophilin-D mediated by sirtuin-3

乌头碱 MPTP公司 SIRT3 线粒体通透性转换孔 锡尔图因 药理学 线粒体 化学 生物化学 细胞凋亡 生物 乙酰化 多巴胺 程序性细胞死亡 内分泌学 多巴胺能 基因
作者
Ningning Wang,Huanhua Xu,Wei Zhou,Hongxing Yang,Jia Wang,Zeng-Chun Ma,Yue Gao
出处
期刊:Journal of Ethnopharmacology [Elsevier BV]
卷期号:270: 113765-113765 被引量:22
标识
DOI:10.1016/j.jep.2020.113765
摘要

Aconite is a processed product of seminal root of perennial herbaceous plant Aconitum Carmichaclii Debx. of Ranunculaceae. It has the effects of warming and tonifying heart yang and restoring yang to save from collapse. Aconitine is the main effective constituent of aconite and used to prevent and treat heart disease. However, how aconitine exerts myocardial protection is still poorly understood. The present study aimed to investigate the effects of aconitine on mitochondrial dysfunction and explore its mechanism of action. The model of myocardial injury was induced by Angiotensin II (Ang II) (1 × 10−6 mol L−1), and H9c2 cells were incubated with different concentrations of aconitine. The effect of aconitine on mitochondrial was determined by flow cytometry, transmission electron microscopy, luciferase, Seahorse technique and Western blot. The effects of aconitine on sirtuin-3 (Sirt3) activity and Cyclophilin D (CypD) acetylation were detected by immunofluorescence, RT-PCR and co-immunoprecipitation. We demonstrate that aconitine alleviates the energy metabolic dysfunction of H9c2 cells by activating Sirt3 to deacetylate CypD and inhibiting mitochondrial permeability transition pore (mPTP) opening. In cardiomyocytes, aconitine significantly reduced mitochondrial fragmentation, inhibited acetylation of CypD, suppressed the mPTP opening, mitigated mitochondrial OXPHOS disorders, and improved the synthesis ability of ATP. In contrast, Sirt3 deficiency abolished the effects of aconitine on mPTP and OXPHOS, indicating that aconitine improves mitochondrial function by activating Sirt3. These results showed that aconitine attenuated the energy metabolism disorder by promoting Sirt3 expression and reducing CypD-mediated mPTP excess openness, rescuing mitochondrial function. Improve mitochondrial function may be a therapeutic approach for treating heart disease, which will generate fresh insight into the cardioprotective of aconitine.
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