Activation of SIRT3 attenuates triptolide-induced toxicity through closing mitochondrial permeability transition pore in cardiomyocytes

• Published in: Toxicology in vitro Vol. 34; pp. 128 - 137
• Main Authors: Yang, Yanqin, Wang, Wenwen, Xiong, Zhewen, Kong, Jiamin, Qiu, Yuwen, Shen, Feihai, Huang, Zhiying
• Format: Journal Article
• Language: English
• Published: England 01.08.2016
• Subjects: Animals; Apoptosis - drug effects; Catalase - metabolism; Cell Line; Cells, Cultured; Diterpenes - toxicity; Epoxy Compounds - toxicity; Forkhead Box Protein O3 - metabolism; Membrane Potential, Mitochondrial - drug effects; Mitochondrial Membrane Transport Proteins - metabolism; Myocytes, Cardiac - drug effects; Myocytes, Cardiac - metabolism; Phenanthrenes - toxicity; Rats, Sprague-Dawley; Reactive Oxygen Species - metabolism; Sirtuins - metabolism; Superoxide Dismutase - metabolism; Cardioprotection; Mitochondrial permeability transition pore; Triptolide; SIRT3
• ISSN: 0887-2333; 1879-3177
• DOI: 10.1016/j.tiv.2016.03.020

Triptolide (TP), an active component of the traditional Chinese herb Tripterygium wilfordii Hook f. (TWHF), has multiple pharmacological effects. However, the severe toxicity of TP greatly restricts its clinical applications. Although TP exposure causes serious heart injury, the mechanism underlying TP-induced cardiotoxicity has rarely been investigated. In previous studies, we found that TP-induced oxidative stress was involved in the mitochondria-dependent apoptosis of cardiomyocytes. Opening of the mitochondrial permeability transition pore (mPTP) is the key to the mitochondrial dysfunction in cardiac toxicity. The aim of this study was to investigate the potential cardioprotective effects of sirtuin 3 (SIRT3) on the mPTP. In the present study, the cytotoxicity of TP was accompanied by the up-regulation of the SIRT3 protein level and its rapid aggregation in nuclei and mitochondria. The SIRT3-FOXO3 signaling pathway was activated simultaneously, resulting in increased transcription of manganese superoxide dismutase (MnSOD) and catalase (CAT) for the elimination of reactive oxygen species (ROS). In addition, augmentation of the SIRT3 level via the overexpression plasmid SIRT3-Flag provided resistance to TP-induced cellular damage, whereas knocking down the SIRT3 level via siRNA accelerated the damage. Because it is an activator of SIRT3, the protective effect of resveratrol was also evaluated in H9c2 cells. In conclusion, the current results suggest that activation of SIRT3 substantially ameliorates the detrimental effects of TP by closing the mPTP.