Association between myocardial calpain activation and apoptosis in lipopolysaccharide-induced septic mouse model.
- Author:
Xiao-ping LI
1
;
Lang LI
;
Rui-zhen CHEN
;
Tang-wei LIU
;
Wei-feng WU
;
E SHEN
;
Ying-zhen YANG
;
Hao-zhu CHEN
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Apoptosis; BH3 Interacting Domain Death Agonist Protein; metabolism; Calcium; metabolism; Calpain; metabolism; Caspase 3; metabolism; Male; Membrane Proteins; Mice; Mice, Inbred C57BL; Myocardium; metabolism; pathology; Proto-Oncogene Proteins; metabolism; Proto-Oncogene Proteins c-bcl-2; Sepsis; metabolism
- From: Chinese Journal of Cardiology 2010;38(9):834-838
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVEin septic mice, myocardial calpain was activated and induced caspase-3 activation, the association between calpain activation and apoptosis was explored in this experiment.
METHODSin in vivo model, adult C57 mice were injected with lipopolysaccharide (LPS, 4 mg/kg, i.p.) to induce sepsis. Myocardial calpain and caspase-3 activities, protein levels of calpain-1, calpain-2, calpastatin, Bcl-2 and Bid were detected by Western blot analysis and myocardial apoptosis was detected by TUNEL, myocardiac function was evaluated by Langendorff system. In in vitro model, adult rat cardiomyocytes were incubated with LPS (1 microg/ml) or co-incubated with calpain inhibitor-III (10 micromol/L), calpain activity, caspase-3 activity, protein levels of Bcl-2 and Bid, and cardiomyocyte apoptosis were detected.
RESULTSin septic mice, myocardial calpain and caspase-3 activity were increased up to 2.7- and 1.8-folds, respectively. Both calpain inhibitor-III and PD150606 significantly attenuated the increase of caspase-3 activity. Myocardial protein levels of calpain-1, calpain-2, calpastatin, Bcl-2 and Bid were similar between control and septic mice, and no cleavage of both Bcl-2 and Bid was found in septic mice. Calpain inhibitor-III significantly improved myocardial function in septic mice. In in vitro model, calpain and caspase-3 activities were increased after 4 h LPS treatment, co-treatment with calpain inhibitor-III prevented caspase-3 activity increase, protein Bcl-2 and Bid were similar between normal cardiomyocytes and LPS-treated cardiomyocytes. Cardiomyocyte apoptosis was similar in in vivo and in vitro septic models.
CONCLUSIONmyocardial calpain activity is increased in LPS induced septic mice, subsequent caspase-3 activation may contribute to myocardial dysfunction in septic mice without aggravating myocardial apoptosis and Bcl-2 and Bid are not involved on calpain induced caspase-3 activation in our model.