共 81 条
Connexin 43 in ischemic pre- and postconditioning
被引:71
作者:

Schulz, Rainer
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h-index: 0
机构: Univ Klinikum Essen, Zentrum Innere Med, Inst Pathophysiol, D-45122 Essen, Germany

Boengler, Kerstin
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h-index: 0
机构: Univ Klinikum Essen, Zentrum Innere Med, Inst Pathophysiol, D-45122 Essen, Germany

Totzeck, Andreas
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h-index: 0
机构: Univ Klinikum Essen, Zentrum Innere Med, Inst Pathophysiol, D-45122 Essen, Germany

Luo, Yukun
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机构: Univ Klinikum Essen, Zentrum Innere Med, Inst Pathophysiol, D-45122 Essen, Germany

Garcia-Dorado, David
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机构: Univ Klinikum Essen, Zentrum Innere Med, Inst Pathophysiol, D-45122 Essen, Germany

Heusch, Gerd
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h-index: 0
机构: Univ Klinikum Essen, Zentrum Innere Med, Inst Pathophysiol, D-45122 Essen, Germany
机构:
[1] Univ Klinikum Essen, Zentrum Innere Med, Inst Pathophysiol, D-45122 Essen, Germany
[2] Hosp Univ Vall Dhebron, Serv Cardiol, Barcelona, Spain
关键词:
Connexin;
43;
ischemic preconditioning;
ischemic postconditioning;
signal transduction;
D O I:
10.1007/s10741-007-9032-3
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Connexin 43 (Cx43) is the predominant protein forming gap junctions and non-junctional hemichannels in ventricular myocardium, but Cx43 is also localized at the inner membrane of cardiomyocyte mitochondria. In cardiomyocytes, Cx43 is involved in the formation of reactive oxygen species, which are central to the signal transduction cascade of ischemic preconditioning's protection. Accordingly, genetically-induced or age-related loss of Cx43 abolishes infarct size reduction by ischemic preconditioning. Similarly, mitochondrial import inhibition of Cx43 completely blocks infarct size reduction by pharmacological preconditioning with diazoxide. In contrast to its importance for preconditioning-induced cardioprotection, Cx43 is not important for infarct size reduction by ischemic postconditioning. In summary, Cx43-especially Cx43 localized in mitochondria-appears to be one key element of the signal transduction cascade of the protection by preconditioning.
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页码:261 / 266
页数:6
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