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5-羟色胺能对受罚行为的控制:中缝核内微量注射氯氮卓、γ-氨基丁酸和5-羟色胺对大鼠行为抑制的影响

Serotoninergic control of punished behavior: effects of intra-raphe microinjections of chlordiazepoxide, GABA and 5-HT on behavioral suppression in rats.

作者信息

Soubrié P, Thiébot M H, Jobert A, Hamon M

出版信息

J Physiol (Paris). 1981;77(2-3):449-53.

PMID:7288658
Abstract

The effects of intra dorsalis raphe microinjections of chlordiazepoxide, GABA and 5-HT were studied on a model of behavioral suppression in rats. The suppression of responding for food was elicited by a 10 min presentation of a signal previously associated with the delivery of electric foot shocks. Microinjections of chlordiazepoxide, GABA and 5-HT (0.2 microliters) performed in awake hand-held rats reduced the behavioral suppression. Chlordiazepoxide and 5-HT acted in a synergistic way, while such a synergy could not be obtained when chlordiazepoxide and GABA were coadministered. Moreover, the effects of intra-raphe chloridazepoxide no longer appeared in rats given intra dorsalis raphe 5-7 dihydroxytryptamine (3 micrograms in 0.4 microliters) 3 weeks before testing. All these results further support the hypothesis of the involvement of 5-HT neurons both in punishment-induced inhibition and in the antipunishment activity of benzodiazepines. No evidence was obtained suggesting a GABAergic mediation for the functional interaction of chlordiazepoxide with 5-HT neurons in this experimental model. Since high 3H-flunitrazepam binding was found at the raphe dorsalis level, and since a 30% decrease in the number of intra-raphe 3H-flunitrazepam binding sites was detected after intra-raphe 5-7 dihydroxytryptamine, it is possible that intra-raphe chlordiazepoxide controls 5-HT neurons partly through some benzodiazepine binding sites located on 5-HT cells.

摘要

研究了在大鼠行为抑制模型中,向中缝背核内微量注射氯氮卓、γ-氨基丁酸(GABA)和5-羟色胺(5-HT)的效果。通过呈现10分钟先前与足部电击相关的信号来引发对食物反应的抑制。在清醒的手持大鼠中进行氯氮卓、GABA和5-HT(0.2微升)的微量注射可减轻行为抑制。氯氮卓和5-HT以协同方式起作用,而氯氮卓和GABA共同给药时则无法获得这种协同作用。此外,在测试前3周给予中缝背核内5,7-二羟基色胺(0.4微升中含3微克)的大鼠中,中缝内氯氮卓的作用不再出现。所有这些结果进一步支持了5-HT神经元参与惩罚诱导的抑制以及苯二氮卓类药物的抗惩罚活性这一假说。在该实验模型中,未获得表明GABA能介导氯氮卓与5-HT神经元功能相互作用的证据。由于在中缝背核水平发现高亲和力的3H-氟硝西泮结合,并且在中缝内注射5,7-二羟基色胺后检测到中缝内3H-氟硝西泮结合位点数量减少30%,因此中缝内氯氮卓可能部分通过位于5-HT细胞上的一些苯二氮卓结合位点来控制5-HT神经元。

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