Effects of taurine on rabbit cardiomyocyte apoptosis during ischemia/reperfusion injury.
- Author:
Ai-ying LI
1
;
En-sheng JI
;
Shu-ming ZHAO
;
Zhi-Hong MA
;
Quan LI
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Apoptosis; drug effects; Apoptosis Regulatory Proteins; metabolism; Male; Myocardial Ischemia; metabolism; pathology; Myocytes, Cardiac; cytology; drug effects; Rabbits; Reperfusion Injury; metabolism; pathology; Taurine; pharmacology
- From: Chinese Journal of Applied Physiology 2004;20(3):224-227
- CountryChina
- Language:Chinese
-
Abstract:
AIMTo study the effect of taurine (Tau) on rabbit cardiomyocyte apoptosis during ischemia/reperfusion (I/R) injury.
METHODSRabbit heart I/R injury was induced by occluding the left anterior descending coronary artery for 45 min and reperfusion for 180 min. taurine (200 mg/kg) was intravenously injected 5 min before heart ischemia. Cardiomyocyte apoptosis was measured by using terminal deoxynucleotidyl transferase--mediated dUTP nick end labeling method (TUNEL), flow cytometry (FCM) and DNA agarose gel electrophoresis.
RESULTSDNA ladder pattern of DNA in myocardium was revealed by agarose gel electrophoresis in I/R group while was not found in Tau + I/R group. Apoptotic cardiomyocytes were sparse within ischemic myocardium at risk in Tau + I/ R group as compared with that in I/R group (TUNEL stain). Apoptosis rate in ischemic myocardium from I/R and Tau + I/R groups detected by flow cytometry was 17.66% +/- 1.54% and 4.86% +/- 1.23%, respectively. Fas and Bax protein expressions in ischemic myocardium of I/R group were higher than that in nonischemic myocardium group (P < 0.01), Bcl-2/Bax ratio in I/R group was lower than that in nonischemic myocardium (P < 0.01); while in Tau + I/R group, Fas and Bax protein expressions were lower than that in I/R group (P < 0.01), the Bcl-2/Bax ratio was higher than that in I/R group (P < 0.01).
CONCLUSIONTaurine reduced apoptosis of myocytes in I/R rabbit heart; its mechanism may involve Fas, Bax and Bcl-2 proteins expression.