Danlou Tablet Protects Against Cardiac Remodeling and Dysfunction after Myocardial Ischemia/Reperfusion Injury through Activating AKT/FoxO3a Pathway

被引:7
作者
Li, Lin [1 ,2 ]
Qi, Weitong [1 ,2 ]
Zhu, Yujiao [1 ,2 ]
Yin, Mingming [1 ,2 ]
Chen, Chen [1 ,2 ]
Wei, Meng [1 ,2 ]
Huang, Zhenzhen [1 ,2 ]
Su, Zhuhua [1 ,2 ]
Jiang, Jizong [1 ,2 ]
Zhang, Mingxue [3 ]
Bei, Yihua [1 ,2 ]
机构
[1] Shanghai Univ, Affiliated Nantong Hosp, Peoples Hosp Nantong 6, Cardiac Regenerat & Ageing Lab,Inst Geriatr,Sch Me, Nantong 226011, Peoples R China
[2] Shanghai Univ, Shanghai Engn Res Ctr Organ Repair, Sch Life Sci, Shanghai 200444, Peoples R China
[3] Liaoning Univ Tradit Chinese Med, Affiliated Hosp, Shenyang 110032, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Danlou tablet; Myocardial ischemia; reperfusion injury; Ventricular remodeling; Cardiomyocyte; AKT; FoxO3a; ISCHEMIA-REPERFUSION INJURY; DEVELOPING RAT-BRAIN; STEM-CELLS; TRANSCRIPTION; GROWTH; HEART; INVOLVEMENT; EXPRESSION; APOPTOSIS; FOXO3A;
D O I
10.1007/s12265-023-10365-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Myocardial ischemia/reperfusion injury (I/RI) and ventricular remodeling are the critical pathological basis of heart failure. Danlou tablet (Dan) is a kind of Chinese patent medicine used in angina pectoris treatment in China. However, it remains unclear whether and how Dan could protect against cardiac remodeling after myocardial I/RI. In this study, both preventive and therapeutic administration of Dan attenuated ventricular remodeling and cardiac dysfunction at 3 weeks after myocardial I/RI. Dan inhibited Bax/Bcl2 ratio and Caspase3 cleavage in heart tissues and also inhibited apoptosis of human AC16 cells and neonatal rat cardiomyocytes stressed by oxygen and glucose deprivation/reperfusion. Mechanistically, Dan inhibited myocardial apoptosis through phosphorylating AKT and FoxO3a, thereby inhibiting downstream BIM and PUMA expressions. Collectively, these results demonstrate that Dan treatment is effective to protect against cardiac remodeling and dysfunction after myocardial I/RI and provide theoretical basis for its cardioprotection and clinical application in treating ischemic cardiac diseases.
引用
收藏
页码:803 / 815
页数:13
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