A functional role for small-conductance calcium-activated potassium channels in sensory pathways including nociceptive processes

被引:64
作者
Bahia, PK
Suzuki, R
Benton, DCH
Jowett, AJ
Chen, MX
Trezise, DJ
Dickenson, AH
Moss, GWJ
机构
[1] UCL, Dept Pharmacol, London WC1E 6BT, England
[2] GlaxoSmithKline Res & Dev Ltd, Stevenage SG1 2NY, Herts, England
基金
英国惠康基金;
关键词
apamin; dorsal root ganglion; sensory transmission; afterhyperpolarization; C-fiber; K(+) channel;
D O I
10.1523/JNEUROSCI.0597-05.2005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated the role of small-conductance calcium-activated potassium (SK) and intermediate-conductance calcium-activated potassium channels in modulating sensory transmission from peripheral afferents into the rat spinal cord. Subunit-specific antibodies reveal high levels of SK3 immunoreactivity in laminas I, II, and III of the spinal cord. Among dorsal root ganglion neurons, both peripherin-positive (C-type) and peripherin-negative (A-type) cells show intense SK3 immunoreactivity. Furthermore, dorsal root-stimulated sensory responses recorded in vitro are inhibited when SK channel activity is increased with 1-ethyl-2-benzimidazolinone (1-EBIO). In vivo electrophysiological recordings show that neuronal responses to naturally evoked nociceptive and nonnociceptive stimuli increase after application of the selective SK channel blocker 8,14-diaza-1,7( 1,4)-diquinolinacyclotetradecaphanedium ditrifluoroacetate (UCL 1848), indicating that SK channels are normally active in moderating afferent input. Conversely, neuronal responses evoked by mechanical stimuli are inhibited when SK channel activity is increased with 1-EBIO. These effects are reversed by the subsequent application of UCL 1848. Our data demonstrate that SK channels have an important role in controlling sensory input into the spinal cord.
引用
收藏
页码:3489 / 3498
页数:10
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