YiXin-Shu, a ShengMai-San-based traditional Chinese medicine formula, attenuates myocardial ischemia/reperfusion injury by suppressing mitochondrial mediated apoptosis and upregulating liver-X-receptor α

被引:54
作者
Zhao, Yichao [1 ]
Xu, Longwei [1 ]
Qiao, Zhiqing [1 ]
Gao, Lingchen [1 ]
Ding, Song [1 ]
Ying, Xiaoying [1 ]
Su, Yuanyuan [1 ]
Lin, Nan [1 ]
He, Ben [1 ]
Pu, Jun [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Ren Ji Hosp, Dept Cardiol, 160 PuJian Rd, Shanghai 200127, Peoples R China
基金
中国国家自然科学基金;
关键词
ISCHEMIA-REPERFUSION INJURY; PREVENTS CARDIOMYOCYTE APOPTOSIS; OXIDATIVE STRESS; PPAR-GAMMA; MELATONIN; PROTECTS; ACTIVATION; EXPRESSION; HEART; INHIBITION;
D O I
10.1038/srep23025
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Positive evidence from clinical trials has fueled growing acceptance of traditional Chinese medicine (TCM) for the treatment of cardiac diseases; however, little is known about the underlying mechanisms. Here, we investigated the nature and underlying mechanisms of the effects of YiXin-Shu (YXS), an antioxidant-enriched TCM formula, on myocardial ischemia/reperfusion (MI/R) injury. YXS pretreatment significantly reduced infarct size and improved viable myocardium metabolism and cardiac function in hypercholesterolemic mice. Mechanistically, YXS attenuated myocardial apoptosis by inhibiting the mitochondrial mediated apoptosis pathway (as reflected by inhibition of mitochondrial swelling, cytochrome c release and caspase-9 activity, and normalization of Bcl-2 and Bax levels) without altering the death receptor and endoplasmic reticulum-stress death pathways. Moreover, YXS reduced oxidative/nitrative stress (as reflected by decreased superoxide and nitrotyrosine content and normalized pro-and anti-oxidant enzyme levels). Interestingly, YXS upregulated endogenous nuclear receptors including LXR alpha, PPAR alpha, PPAR beta and ER alpha, and in-vivo knockdown of cardiac-specific LXR alpha significantly blunted the cardio-protective effects of YXS. Collectively, these data show that YXS is effective in mitigating MI/R injury by suppressing mitochondrial mediated apoptosis and oxidative stress and by upregulating LXR alpha, thereby providing a rationale for future clinical trials and clinical applications.
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页数:13
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共 60 条
[1]   The Effect of Crataegus Fruit Extract and Some of its Flavonoids on Mitochondrial Oxidative Phosphorylation in the Heart [J].
Bernatoniene, J. ;
Trumbeckaite, S. ;
Majiene, D. ;
Baniene, R. ;
Baliutyte, G. ;
Savickas, A. ;
Toleikis, A. .
PHYTOTHERAPY RESEARCH, 2009, 23 (12) :1701-1707
[2]   New paradigms in the treatment of hepatic cholestasis: From UDCA to FXR, PXR and beyond [J].
Beuers, Ulrich ;
Trauner, Michael ;
Jansen, Peter ;
Poupon, Raoul .
JOURNAL OF HEPATOLOGY, 2015, 62 :S25-S37
[3]   Anatomical profiling of nuclear receptor expression reveals a hierarchical transcriptional network [J].
Bookout, Angie L. ;
Jeong, Yangsik ;
Downes, Michael ;
Yu, Ruth T. ;
Evans, Ronald M. ;
Mangelsdorf, David J. .
CELL, 2006, 126 (04) :789-799
[4]   Enhanced Skeletal Muscle Expression of Extracellular Superoxide Dismutase Mitigates Streptozotocin-Induced Diabetic Cardiomyopathy by Reducing Oxidative Stress and Aberrant Cell Signaling [J].
Call, Jarrod A. ;
Chain, Kristopher H. ;
Martin, Kyle S. ;
Lira, Vitor A. ;
Okutsu, Mitsuharu ;
Zhang, Mei ;
Yan, Zhen .
CIRCULATION-HEART FAILURE, 2015, 8 (01) :188-197
[5]   Melatonin-enhanced autophagy protects against neural apoptosis via a mitochondrial pathway in early brain injury following a subarachnoid hemorrhage [J].
Chen, Jingyin ;
Wang, Lin ;
Wu, Cheng ;
Hu, Qiang ;
Gu, Chi ;
Yan, Feng ;
Li, Jianru ;
Yan, Wei ;
Chen, Gao .
JOURNAL OF PINEAL RESEARCH, 2014, 56 (01) :12-19
[6]   Yindanxinnaotong, a Chinese compound medicine, synergistically attenuates atherosclerosis progress [J].
Cheng, Long ;
Pan, Guo-feng ;
Zhang, Xiao-dong ;
Wang, Jian-lu ;
Wang, Wan-dan ;
Zhang, Jian-yong ;
Wang, Hui ;
Liang, Ri-xin ;
Sun, Xiao-bo .
SCIENTIFIC REPORTS, 2015, 5
[7]   Regulator of G-protein signalling 5 protects against atherosclerosis in apolipoprotein E-deficient mice [J].
Cheng, Wen-Lin ;
Wang, Pi-Xiao ;
Wang, Tao ;
Zhang, Yan ;
Du, Cheng ;
Li, Hongliang ;
Ji, Yong .
BRITISH JOURNAL OF PHARMACOLOGY, 2015, 172 (23) :5676-5689
[8]   Biological ingredient analysis of traditional Chinese medicine preparation based on high-throughput sequencing: the story for Liuwei Dihuang Wan [J].
Cheng, Xinwei ;
Su, Xiaoquan ;
Chen, Xiaohua ;
Zhao, Huanxin ;
Bo, Cunpei ;
Xu, Jian ;
Bai, Hong ;
Ning, Kang .
SCIENTIFIC REPORTS, 2014, 4
[9]   Cardioprotective effect of dipeptidyl peptidase-4 inhibitor during ischemia-reperfusion injury [J].
Chinda, Kroekkiat ;
Palee, Siripong ;
Surinkaew, Sirirat ;
Phornphutkul, Mattabhorn ;
Chattipakorn, Siriporn ;
Chattipakorn, Nipon .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2013, 167 (02) :451-457
[10]   Murine atrial HL-1 cell line is a reliable model to study drug metabolizing enzymes in the heart [J].
Elshenawy, Osama H. ;
Anwar-Mohamed, Anwar ;
Abdelhamid, Ghada ;
El-Kadi, Ayman O. S. .
VASCULAR PHARMACOLOGY, 2013, 58 (04) :326-333