The role of MAP kinases in trauma and ischemia-reperfusion

被引:26
作者
Lai, EW
Toledo-Pereyra, LH
Walsh, J
Lopez-Neblina, F
Anaya-Prado, R
机构
[1] Michigan State Univ, Borgess Res Inst, Kalamazoo Ctr Med Studies, Kalamazoo, MI 49048 USA
[2] Michigan State Univ, E Lansing, MI 48824 USA
关键词
ERK; ischemia-reperfusion; MAPKs; p38; SAP/JNK; trauma;
D O I
10.1080/08941930490269646
中图分类号
R61 [外科手术学];
学科分类号
摘要
Mitogen-activated protein kinases (MAPKs) have been the focus of a number of studies, as these compounds are involved in a number of important inflammatory cell signaling mechanisms. Recent studies have further elucidated the role of MAPKs in the inflammatory response, as a result of trauma and/or ischemia-reperfusion (I/R) injury. There are three major classes of MAPKs that may be involved in the inflammatory response: extracellular signal-regulated kinases (ERKs), stress-activated protein kinases (SAPKs)/c-Jun NH 2 -terminal kinases (JNKs), and p38 MAPKs (p38). This is clinically relevant, because these pathways may be a possible target for anti-inflammatory drug intervention. This review studies the role of MAPKs in trauma and/or I/R.
引用
收藏
页码:45 / 53
页数:9
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