Tyrosine kinase signaling in action potential shortening and expression of HSP72 in late preconditioning

被引:14
作者
Okubo, S
Bernardo, NL
Elliott, GT
Hess, ML
Kukreja, RC
机构
[1] Virginia Commonwealth Univ, Med Coll Virginia, Div Cardiol, Dept Med, Richmond, VA 23298 USA
[2] Kanazawa Med Univ, Dept Cardiol, Kahoku, Ishikawa 9200293, Japan
[3] Corixa Corp, Hamilton, MT 59840 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2000年 / 279卷 / 05期
关键词
genistein; adenosine 5 '-triphosphate-sensitive potassium; channel; ischemia-reperfusion; 72-kDa heat shock protein;
D O I
10.1152/ajpheart.2000.279.5.H2269
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We investigated the role of tyrosine kinase (TK) signaling in the opening of the ATP-sensitive K+ (K-ATP) channel and 72-kDa heat shock protein (HSP72) expression during late preconditioning. Rabbits were subjected to surgical operation (sham) or were preconditioned (PC) with four cycles of 5 min of ischemia and 10 min of reperfusion. Twenty-four hours later, animals were subjected to 30 min of ischemia and 180 min of reperfusion. Genistein (1 mg/ kg ip) was used to block the receptor TK. Six groups were studied: control, sham, genistein-sham, PC, genistein-PC, and vehicle-PC group (1% dimethyl sulfoxide). Genistein or vehicle was given 30 min before the surgical procedure. Genistein pretreatment decreased the expression of HSP72 in PC hearts and suppressed action potential duration shortening during ischemia in sham and PC groups. Infarct size (% risk area) was reduced in the PC (11.6 +/- 1.0%) and vehicle-PC (19.3 +/- 2.0%) compared with the control (40.0 +/- 3.8%) or sham (46.0 +/- 2.0%) groups (P < 0.05). Genistein pretreatment increased infarct size to 46.4 +/- 4.1% in the PC hearts. We conclude that TK signaling is involved in K-ATP channel opening and HSP72 expression during late PC.
引用
收藏
页码:H2269 / H2276
页数:8
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