Qiangxinyin formula protects against isoproterenol-induced cardiac hypertrophy

被引:0
|
作者
Zhou, Zhong-Yan [1 ,2 ,3 ]
Ma, Jie [1 ,4 ]
Zhao, Wai-Rong [1 ]
Shi, Wen -Ting [1 ]
Zhang, Jing [1 ]
Hu, Yan-Yan [1 ]
Yue, Mei-Yan [1 ]
Zhou, Wen-Long [1 ]
Yan, Hua [5 ]
Tang, Jing-Yi [1 ]
Wang, Yu [2 ,3 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Longhua Hosp, Shanghai, Peoples R China
[2] Univ Hong Kong, Dept Pharmacol & Pharm, Hong Kong Special Adm Reg China, 2-F Lab Block,21 Sassoon Rd, Hong Kong, Peoples R China
[3] Univ Hong Kong, State Key Lab Pharmaceut Biotechnol, Hong Kong Special Adm Reg China, Hong Kong, Peoples R China
[4] Shanghai Univ Tradit Chinese Med, Sch Acupuncture Moxibust & Tuina, Shanghai, Peoples R China
[5] Shanghai Univ Tradit Chinese Med, Shuguang Hosp, Shanghai, Peoples R China
关键词
Heart failure; Cardiac fibrosis; Cardiac hypertrophy; Calcium overload; Traditional Chinese medicine; Zebrafish; ZEBRAFISH; CYTOSKELETON; DYSFUNCTION; METABOLISM; GLYCOSIDES;
D O I
10.1016/j.phymed.2024.155717
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Heart failure is a life-threatening cardiovascular disease and characterized by cardiac hypertrophy, inflammation and fibrosis. The traditional Chinese medicine formula Qiangxinyin (QXY) is effective for the treatment of heart failure while the underlying mechanism is not clear. This study aims to identify the active ingredients of QXY and explore its mechanisms protecting against cardiac hypertrophy. We found that QXY significantly protected against isoproterenol (ISO)-induced cardiac hypertrophy and dysfunction in zebrafish. Eight compounds, including benzoylmesaconine (BMA), atractylenolide I (ATL I), icariin (ICA), quercitrin (QUE), psoralen (PRN), kaempferol (KMP), ferulic acid (FA) and protocatechuic acid (PCA) were identified from QXY. PRN, KMP and icaritin (ICT), an active pharmaceutical ingredient of ICA, prevented ISO-induced cardiac hypertrophy and dysfunction in zebrafish. In H9c2 cardiomyocyte treated with ISO, QXY significantly blocked the calcium influx, reduced intracellular lipid peroxidative product MDA, stimulated ATP production and increased mitochondrial membrane potential. QXY also inhibited ISO-induced cardiomyocyte hypertrophy and cytoskeleton reorganization. Mechanistically, QXY enhanced the phosphorylation of Smad family member 2 (SMAD2) and myosin phosphatase target subunit-1 (MYPT1), and suppressed the phosphorylation of myosin light chain (MLC). In conclusion, PRN, KMP and ICA are the main active ingredients of QXY that protect against ISO-induced cardiac hypertrophy and dysfunction largely via the blockage of calcium influx and inhibition of mitochondrial dysfunction as well as cytoskeleton reorganization.
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页数:14
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