Simvastatin ameliorates rat ventricular remodeling after myocardial infarction:the role of phosphorylating extracellular signal-regulated kinase1/2
Maohui Zhang
Abstract
Maohui Zhang
Abstract
Aim To study the effect of simvastatin on ventricular remodeling in rats after myocardial infarction,and the association between this effect and phosphorylating extracellular signal-regulated kinase1/2(p-ERK1/2).Methods Myocardial infarction(MI)rat models were successfully induced by ligation of anterior descending coronary artery.The treated rats were randomly divided into 4 groups(n=8~10):MI only group,MI plus 20 mg Sim group(20 mg·kg-1·d-1),MI plus 40 mg Sim group(40 mg·kg-1·d-1),and sham-operated group.After 4 weeks,the rats were checked by echocardiography including LVEDd,LVPWd,LVEF,FS,SV and CO.Myocardial p-ERK1/2 was also examined by immunohistochemistry and Western blot.Results Compared with sham-operated group,LVEDd,LVPWd in other groups were significantly increased(P0.01),and LVEF,FS,SV and CO were significantly reduced(P0.01).However,simvastatin significantly decreased LVEDd,LVPWd(P0.01),and increased LVEF,FS,SV and CO(P0.01)compared with MI only group.MI significantly increased(P0.01)myocardial p-ERK1/2 expression,while simvastatin dose dependently inhibited myocardial p-ERK1/2 expression.Conclusion Simvastatin ameliorated left ventricular remodeling and heart function after MI in rats,which was associated with the effect of decreasing myocardial p-ERK1/2 expression.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Aim To study the effect of simvastatin on ventricular remodeling in rats after myocardial infarction,and the association between this effect and phosphorylating extracellular signal-regulated kinase1/2(p-ERK1/2).Methods Myocardial infarction(MI)rat models were successfully induced by ligation of anterior descending coronary artery.The treated rats were randomly divided into 4 groups(n=8~10):MI only group,MI plus 20 mg Sim group(20 mg·kg-1·d-1),MI plus 40 mg Sim group(40 mg·kg-1·d-1),and sham-operated group.After 4 weeks,the rats were checked by echocardiography including LVEDd,LVPWd,LVEF,FS,SV and CO.Myocardial p-ERK1/2 was also examined by immunohistochemistry and Western blot.Results Compared with sham-operated group,LVEDd,LVPWd in other groups were significantly increased(P0.01),and LVEF,FS,SV and CO were significantly reduced(P0.01).However,simvastatin significantly decreased LVEDd,LVPWd(P0.01),and increased LVEF,FS,SV and CO(P0.01)compared with MI only group.MI significantly increased(P0.01)myocardial p-ERK1/2 expression,while simvastatin dose dependently inhibited myocardial p-ERK1/2 expression.Conclusion Simvastatin ameliorated left ventricular remodeling and heart function after MI in rats,which was associated with the effect of decreasing myocardial p-ERK1/2 expression.
Key concepts: Simvastatin, Myocardial infarction, Ventricular remodeling, Internal medicine, Cardiology, Ligation, Ejection fraction, Medicine