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白藜芦醇抑制遭受缺氧/复氧损伤的心肌细胞中的自噬:涉及电压依赖性阴离子通道1/PTEN诱导激酶1/帕金蛋白途径。

Resveratrol inhibits autophagy in cardiomyocytes subjected anoxia/reoxygenation injury: involved in VDAC1/PINK1/Parkin pathway.

作者信息

Zhou Ying, Huang Yongzhe, Liang Haiyan, Yang Xiaomei, Zhang Shulin, Huang Yinru, Wan Yanping, Zhou Hangfei, Huang An, Chen Yue, Li Xiao, Peng Yian, Liao Zhangping

机构信息

Jiangxi Provincial Key Laboratory of Drug Target Discovery and Validation, School of Pharmacy, Jiangxi Medical College, Nanchang University, Nanchang 330031, PR China; The MOE Basic Research and Innovation Center for the Targeted Therapeutics of Solid Tumors, Jiangxi Medical College, Nanchang University, Nanchang, PR China.

Jiangxi Provincial Key Laboratory of Drug Target Discovery and Validation, School of Pharmacy, Jiangxi Medical College, Nanchang University, Nanchang 330031, PR China; The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang 330006, PR China.

出版信息

Toxicol Appl Pharmacol. 2025 Sep;502:117421. doi: 10.1016/j.taap.2025.117421. Epub 2025 May 29.

Abstract

Resveratrol has confirmed effectiveness in alleviating myocardial ischemia/reperfusion(I/R) injury. However, the underlying mechanisms remain unclear. Mitochondrial dysfunction in injured cardiomyocytes activates autophagy, and excessive autophagy during reperfusion implicates aggravated injury. Considering that resveratrol preserves mitochondrial function by down-regulating VDAC1 expression, we speculated that the cardioprotective effect of resveratrol is achieved by mitochondrial regulation, and we wonder whether it is accomplished by ultimately modulating autophagy. Therefore, this study investigated the mechanism of resveratrol against myocardial I/R injury regarding autophagy regulation and explored the signal pathway. Herein, we established an anoxia/reoxygenation(A/R) model to simulate myocardial I/R injury in vitro. The expressions of VDAC1, Beclin1, LC3-II/I, Parkin, and PINK1 were detected by Western blot; the LDH activity and mPTP opening were measured by spectrophotometry; the ROS levels and mitochondrial membrane potential (ΔΨm) were examined by flow cytometry; the sublocalisation of Parkin and the autophagic vacuoles (AVs) were observed by laser confocal microscopy. Results suggested that resveratrol attenuated A/R injury by inhibiting autophagy, manifested as lower LDH activity, higher cell viability with decreased LC3-II/LC3-I ratio, down-regulated Beclin1 expression, and reduced number of AVs. In addition, stabilised mitochondrial membrane potential, inhibited ROS production and mPTP opening indicated maintained mitochondrial homeostasis. Compared with the A/R group, resveratrol pretreatment down-regulated the PINK1, Parkin, and VDAC1 expressions, accompanied by decreased colocalization of mitochondria with Parkin, suggesting the involved PINK1/Parkin signal pathway. Transfection with pFLAG-VDAC1 reversed resveratrol-induced mitophagy inhibition and cardioprotection. In conclusion, resveratrol protects cardiomyocytes by inhibiting excessive autophagy induced by the VDAC1/PINK1/Parkin pathway during A/R injury.

摘要

白藜芦醇已被证实对减轻心肌缺血/再灌注(I/R)损伤有效。然而,其潜在机制仍不清楚。受损心肌细胞中的线粒体功能障碍会激活自噬,而再灌注期间过度的自噬意味着损伤加剧。鉴于白藜芦醇通过下调电压依赖性阴离子通道1(VDAC1)的表达来维持线粒体功能,我们推测白藜芦醇的心脏保护作用是通过线粒体调节实现的,并且想知道它是否最终通过调节自噬来完成。因此,本研究探讨了白藜芦醇抗心肌I/R损伤在自噬调节方面的机制,并探索了信号通路。在此,我们建立了缺氧/复氧(A/R)模型以在体外模拟心肌I/R损伤。通过蛋白质免疫印迹法检测VDAC1、Beclin1、微管相关蛋白1轻链3-II/I(LC3-II/I)、帕金蛋白(Parkin)和无柄小泡蛋白1(PINK1)的表达;通过分光光度法测量乳酸脱氢酶(LDH)活性和线粒体通透性转换孔(mPTP)开放情况;通过流式细胞术检测活性氧(ROS)水平和线粒体膜电位(ΔΨm);通过激光共聚焦显微镜观察Parkin的亚定位和自噬泡(AVs)。结果表明,白藜芦醇通过抑制自噬减轻A/R损伤,表现为较低的LDH活性、较高的细胞活力、LC3-II/LC3-I比值降低、Beclin1表达下调以及AVs数量减少。此外,稳定的线粒体膜电位、抑制ROS产生和mPTP开放表明线粒体稳态得以维持。与A/R组相比,白藜芦醇预处理下调了PINK1、Parkin和VDAC1的表达,同时线粒体与Parkin共定位减少,提示PINK1/Parkin信号通路参与其中。用pFLAG-VDAC1转染可逆转白藜芦醇诱导的线粒体自噬抑制和心脏保护作用。总之,白藜芦醇通过抑制A/R损伤期间由VDAC1/PINK1/Parkin途径诱导的过度自噬来保护心肌细胞。

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