Modulation of CGRP and PGE2 release from isolated rat skin by α-adrenoceptors and κ-opioid-receptors

被引:27
作者
Averbeck, B
Reeh, PW [1 ]
Michaelis, M
机构
[1] Univ Erlangen Nurnberg, Dept Physiol & Expt Pathophysiol, D-91054 Erlangen, Germany
[2] Univ Kiel, Dept Physiol, D-24098 Kiel, Germany
关键词
asimadoline; neurogenic inflammation; neuropeptides; norepinephrine; pain;
D O I
10.1097/00001756-200107200-00011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Norepinephrine (NE) reduces the release of neuropeptides from central terminals of primary afferent neurones by presynaptic inhibition. We investigated whether NE also affects stimulus-induced intracutaneous calcitonin gene-related peptide (CGRP) and secondary prostaglandin E-2 (PGE(2)) release. For comparison. kappa -opioid effects were examined. Antidromic electrical nerve stimulation resulted in significant increases in the release of CGRP and PGE(2). The PGE(2) release was prevented by selective activation of alpha (2)-adrenoceptors whereas the CGRP release was not changed. In contrast, selective kappa -opioid receptor activation diminished electrically evoked release of both CGRP and PGE-(2). We conclude that NE affected stimulated PGE(2) release via alpha (2)-adrenoceptors on cells other than cutaneous afferents while kappa -opioid receptors are expressed in peripheral terminals of cutaneous afferents and their activation reduced CGRP release and secondary PGE(2) formation. NeuroReport 12:2097-2100 (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:2097 / 2100
页数:4
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