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大鼠中缝隐核向导水管周围灰质神经元的5-羟色胺能影响

Serotonergic influence from nucleus raphe obscurus on neurones in the periaqueductal grey matter in the rat.

作者信息

Lovick T A

机构信息

Department of Physiology, Medical School, University of Birmingham, UK.

出版信息

Brain Res. 1993 Mar 19;606(1):92-8. doi: 10.1016/0006-8993(93)91574-c.

Abstract

In rats anaesthetised with urethane, iontophoretic application of 5-hydroxytryptamine (5-HT, 5-70 nA) produced changes in ongoing activity of 41/44 neurones in the periaqueductal grey matter (PAG). The majority (85%) of responsive cells were inhibited and 15% were excited. The inhibitions were mimicked in 5/7 cells by iontophoresis of the 5-HT1A agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT, 10-30 nA) whilst excitation was produced in 3/5 cells by iontophoresis of the 5-HT2 agonist alpha-methyl-5-HT (10-30 nA). Selective activation of neuronal perikarya in nucleus raphe obscurus (NRO) by microinjection of 50-100 nl D,L-homocysteic acid (DLH) inhibited ongoing activity of 25/31 neurones tested in the PAG for periods of 30-580 s, mean 183.5 s. The duration of the inhibition was potentiated by between 36 and 300% during iontophoresis of the 5-HT re-uptake blocker paroxetine (1-25 nA, 6/6 cells). The results indicate that there is an extensive inhibitory serotonergic input to the PAG which originates, at least in part, from NRO.

摘要

在用乌拉坦麻醉的大鼠中,离子导入5-羟色胺(5-HT,5-70 nA)可使中脑导水管周围灰质(PAG)中44个神经元中的41个神经元的自发放电活动发生改变。大多数反应性细胞(85%)受到抑制,15%被兴奋。5-HT1A激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT,10-30 nA)离子导入可模拟5/7个细胞中的抑制作用,而5-HT2激动剂α-甲基-5-HT(10-30 nA)离子导入可使3/5个细胞产生兴奋。通过微量注射50-100 nl D,L-高半胱氨酸(DLH)选择性激活中缝隐核(NRO)中的神经元胞体,可抑制PAG中31个被测试神经元中的25个神经元的自发放电活动30-580秒,平均183.5秒。在离子导入5-HT再摄取阻滞剂帕罗西汀(1-25 nA,6/6个细胞)期间,抑制持续时间增强了36%至300%。结果表明,PAG存在广泛的抑制性血清素能输入,至少部分起源于NRO。

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