Regulation of calcitonin gene-related peptide release from rat trigeminal nucleus caudalis slices in vitro

被引:48
作者
Jenkins, DW
Langmead, CJ
Parsons, AA
Strijbos, PJ
机构
[1] GlaxoSmithKline, Neurol Ctr Excellence Drug Discovery, Harlow CM19 5AW, Essex, England
[2] GlaxoSmithKline, Psychiat Ctr Excellence Drug Discovery, Harlow CM19 5AW, Essex, England
关键词
prostaglandin E-2; migraine; trigeminal nucleus caudalis; calcitonin gene-related peptide; superfusion;
D O I
10.1016/j.neulet.2004.05.067
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Calcitonin gene-related peptide (CGRP) released from trigeminal primary afferents has been implicated in the pathophysiology of migraine. Here, we have used an in vitro slice preparation to investigate its release from nerve terminals in the rat trigeminal nucleus caudalis. Extracellular-calcium dependent CGRP release was stimulated by both capsaicin and neuronal depolarization with KCl. The capsaicin (1 muM)-evoked CGRP release was blocked by capsazepine and was also attenuated in the presence of the cyclooxygenase inhibitor, indomethacin, an effect that was reversed when slices were stimulated with capsaicin in the presence of the cyclooxygenase metabolite, prostaglandin E-2. Taken together, these data further highlight the importance of prostaglandins as enhancers of neuropeptide release and suggest that CGRP released from the central terminals of trigeminal neurones has the potential to be involved in the transmission of nociceptive information of relevance to migraine headache. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:241 / 244
页数:4
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