Apoptosis in pressure overload-induced heart hypertrophy in the rat

被引:347
|
作者
Teiger, E
Dam, TV
Richard, L
Wisnewsky, C
Tea, BS
Gaboury, L
Tremblay, J
Schwartz, K
Hamet, P
机构
[1] UNIV MONTREAL,CTR RECH,MOLEC PATHOPHYSIOL LAB,HOP HOTEL DIEU,MONTREAL,PQ H2W 1T8,CANADA
[2] HOP LA PITIE SALPETRIERE,INSERM UR153,F-75651 PARIS 13,FRANCE
来源
JOURNAL OF CLINICAL INVESTIGATION | 1996年 / 97卷 / 12期
关键词
apoptosis; heart; hypertrophy; aortic stenosis; pressure overload;
D O I
10.1172/JCI118747
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Pressure overload induces cardiac growth in the rat, which implies the hypertrophy of cardiac muscle cells and proliferation of nonmuscle cells, The cardiac cell loss observed in parallel has generally been attributed to necrosis. Using an in situ assay, we demonstrated a phase of apoptosis or programmed cell death during the first 7 d after pressure overload with a peak at day 4 while cardiac growth continued for over 30 d, The increase in apoptosis was confirmed by quantification of 180-1500-bp DNA oligonucleosomes with agarose get electrophoresis and in situ labeling via 3'-terminal deoxynucleotidyl transferase assay. While some apoptosis was observed in the basal state in nonmuscle cells, pressure overload induced apoptosis mainly in cardiomyocytes. These data suggest that cardiac hypertrophy is initiated by a wave of apoptosis of cardiomyocytes. Thus, apoptosis may be involved in the pathogenesis of heart remodeling.
引用
收藏
页码:2891 / 2897
页数:7
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