Posttranslational mechanisms of peripheral sensitization

被引:113
作者
Bhave, G
Gereau, RW
机构
[1] Washington Univ, Sch Med, Pain Ctr, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Anesthesiol, St Louis, MO 63110 USA
[3] Baylor Coll Med, Div Neurosci, Houston, TX 77030 USA
来源
JOURNAL OF NEUROBIOLOGY | 2004年 / 61卷 / 01期
关键词
ion channel; capsaicin; TRPV1; TTX4; pain; phosphorylation; CaMKII; PKA; PKC; ERK;
D O I
10.1002/neu.20083
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The sensation of pain can be dramatically altered in response to injury or disease. This sensitization can occur at the level of the primary sensory neuron, and can be mediated by multiple biochemical mechanisms, including, but not limited to, changes in gene transcription, changes in translation, stability, or subcellular localization of translated proteins, and post-translational modifications. This review focuses on post-translational modifications to ion channels expressed in primary sensory neurons that form the machinery driving peripheral sensitization and pain hypersensitivity. Studies published to date show strong evidence for modulation of ion channels involved in transduction and transmission of nociceptive inputs coincident with biophysical and behavioral sensitization. The roles of phosphorylation and oxidation/reduction reactions of voltage-dependent sodium, potassium, and calcium channels are discussed, as well as phosphorylation-mediated modulation of sensory transduction channels. (C) 2004 Wily Periodicals, Inc.
引用
收藏
页码:88 / 106
页数:19
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