Mechanisms of acetylcholine- and bradykinin-induced preconditioning

被引:31
作者
Critz, SD
Cohen, MV
Downey, JM
机构
[1] Univ S Alabama, Coll Med, Dept Cell Biol & Neurosci, Mobile, AL 36688 USA
[2] Univ S Alabama, Coll Med, Dept Physiol, Mobile, AL 36688 USA
[3] Univ S Alabama, Coll Med, Dept Med, Mobile, AL USA
关键词
ischemic preconditioning; pharmacological preconditioning; reactive oxygen species; protein kinase; mitochondria; PI3-kinase; ATP-sensitive potassium channels; Akt; nitric oxide;
D O I
10.1016/j.vph.2005.02.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Acetylcholine (ACh) and bradykinin (BK) are potent pharmacological agents which mimic ischemic preconditioning (IPC) enabling, hearts to resist infarction during a subsequent period of ischemia. The cardioprotective pathways activated by BK but not ACh may also protect when activated at reperfusion. ACh and BK stimulate G(i/o)-linked receptors and ultimately mediate protection by opening mitochondrial ATP-sensitive potassium channels with the generation of reactive oxygen species that act as second messengers to activate protein kinase C (PKC). There appear to be key differences, however, in the pathways prior to potassium channel opening for these two receptors. This review aims to summarize what is currently known about pharmacological preconditioning by ACh and BK with an emphasis on differences that are seen in the signal transduction cascades. Understanding the cellular basis of protection by ACh and BK is a critical step towards developing pharmacological agents that will prevent infarction during ischemia resulting from coronary occlusion or heart attack. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:201 / 209
页数:9
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