Bawei Chenxiang Wan Ameliorates Cardiac Hypertrophy by Activating AMPK/PPAR-α Signaling Pathway Improving Energy Metabolism

被引:14
|
作者
Zhang, Xiaoying [1 ]
Zhang, Zhiying [1 ]
Wang, Pengxiang [1 ]
Han, Yiwei [1 ]
Liu, Lijun [1 ]
Li, Jie [1 ]
Chen, Yichun [1 ]
Liu, Duxia [1 ]
Wang, Jinying [2 ]
Tian, Xiaoying [2 ]
Zhao, Qin [1 ]
Yan, Fengxia [2 ]
机构
[1] Xizang Minzu Univ, Sch Med, Dept Pharmacol, Xianyang, Peoples R China
[2] Jinan Univ, Sch Med Sci, Guangzhou, Peoples R China
来源
FRONTIERS IN PHARMACOLOGY | 2021年 / 12卷
基金
中国国家自然科学基金;
关键词
cardiac hypertrophy; energy metabolism; Bawei Chenxiang Wan; isoprenaline; AMPK; PPAR-alpha; CONTRACTILE RESERVE; HEART-FAILURE; MECHANISMS; FIBROSIS; AMPK; PHOSPHORYLATION; ACCUMULATION; INFLAMMATION; DYSFUNCTION; DISEASE;
D O I
10.3389/fphar.2021.653901
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Bawei Chenxiang Wan (BCW), a well-known traditional Chinese Tibetan medicine formula, is effective for the treatment of acute and chronic cardiovascular diseases. In the present study, we investigated the effect of BCW in cardiac hypertrophy and underlying mechanisms. The dose of 0.2, 0.4, and 0.8 g/kg BCW treated cardiac hypertrophy in SD rat model induced by isoprenaline (ISO). Our results showed that BCW (0.4 g/kg) could repress cardiac hypertrophy, indicated by macro morphology, heart weight to body weight ratio (HW/BW), left ventricle heart weight to body weight ratio (LVW/BW), hypertrophy markers, heart function, pathological structure, cross-sectional area (CSA) of myocardial cells, and the myocardial enzymes. Furthermore, we declared the mechanism of BCW anti-hypertrophy effect was associated with activating adenosine 5'-monophosphate (AMP)-activated protein kinase (AMPK)/peroxisome proliferator-activated receptor-alpha (PPAR-alpha) signals, which regulate carnitine palmitoyltransferase1 beta (CPT-1 beta) and glucose transport-4 (GLUT-4) to ameliorate glycolipid metabolism. Moreover, BCW also elevated mitochondrial DNA-encoded genes of NADH dehydrogenase subunit 1(ND1), cytochrome b (Cytb), and mitochondrially encoded cytochrome coxidase I (mt-co1) expression, which was associated with mitochondria function and oxidative phosphorylation. Subsequently, knocking down AMPK by siRNA significantly can reverse the anti-hypertrophy effect of BCW indicated by hypertrophy markers and cell surface of cardiomyocytes. In conclusion, BCW prevents ISO-induced cardiomyocyte hypertrophy by activating AMPK/PPAR-alpha to alleviate the disturbance in energy metabolism. Therefore, BCW can be used as an alternative drug for the treatment of cardiac hypertrophy.
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页数:14
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