Dickie B G, Greenfield S A
University Department of Pharmacology, Oxford, UK.
Neuroreport. 1994 Mar 21;5(7):769-72. doi: 10.1097/00001756-199403000-00008.
Acetylcholinesterase (AChE) is released from dopaminergic dendrites in the guinea-pig substantia nigra. This release, measured by a chemiluminescent assay, is increased following electrical stimulation of the dorsal raphé nucleus, which sends a 5-hydroxytryptaminergic input to the substantia nigra. Application of exogenous 5-hydroxytryptamine (5-HT) directly to the substantia nigra similarly enhanced release of AChE, whilst local application of cinanserin, a 5-HT antagonist, inhibited electrically-evoked release. Although the substantia nigra posseses a dense localization of 5-HT1D receptors, application of the 5-HT1D agonist sumatriptan did not effect AChE release. The results indicate that 5-HT, released from raphé-nigral afferent nerves, enhances the dendritic release of AChE, although this effect is unlikely to be mediated via 5-HT1D receptors.
乙酰胆碱酯酶(AChE)从豚鼠黑质的多巴胺能树突中释放。通过化学发光测定法测得,在对中缝背核进行电刺激后,这种释放会增加,中缝背核向黑质发送5-羟色胺能输入。将外源性5-羟色胺(5-HT)直接应用于黑质同样会增强AChE的释放,而局部应用5-HT拮抗剂西那色林则会抑制电诱发的释放。尽管黑质中5-HT1D受体密集分布,但应用5-HT1D激动剂舒马曲坦对AChE释放没有影响。结果表明,从中缝-黑质传入神经释放的5-HT会增强AChE的树突状释放,尽管这种作用不太可能通过5-HT1D受体介导。