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组胺对清醒及经戊巴比妥预处理的大鼠的唤醒作用。

Histamine-induced arousal in the conscious and pentobarbital-pretreated rat.

作者信息

Kalivas P W

出版信息

J Pharmacol Exp Ther. 1982 Jul;222(1):37-42.

PMID:7086707
Abstract

Histamine has been shown to possess many neurotransmitter-like properties, and a variety of studies indicate that central histamine may function in modulating behavioral arousal. To examine this possibility further, histamine was administered into the lateral cerebral ventricles of the conscious and pentobarbital-anesthetized rat. In the conscious animal, histamine induced a significant increase in spontaneous motor activity which consisted of increased grooming and exploratory behaviors (sniffing, rearing and locomotion) as compared to saline-treated controls. In the pentobarbital-pretreated rat, histamine caused a dose-related decrease in narcosis duration and hypothermia without altering the disposition of pentobarbital in brain or plasma. Administration of compounds structurally related to histamine did not alter spontaneous activity or shorten narcosis duration. While pretreatment with the H2-histamine antagonist, cimetidine, was no effective, H1-histamine antagonists were found to abolish histamine-induced arousal. Administration of haloperidol in doses that significantly attenuated increased spontaneous motor activity by amphetamine did not alter histamine-induced hyperactivity. Likewise, atropine did not significantly alter histamine-induced arousal. These data support the hypothesis that histamine may function in modulating behavioral arousal.

摘要

组胺已被证明具有许多类似神经递质的特性,并且各种研究表明中枢组胺可能在调节行为觉醒中发挥作用。为了进一步研究这种可能性,将组胺注入清醒和戊巴比妥麻醉大鼠的侧脑室。在清醒动物中,与生理盐水处理的对照组相比,组胺诱导自发运动活动显著增加,包括理毛和探索行为(嗅探、竖毛和运动)增加。在戊巴比妥预处理的大鼠中,组胺导致麻醉持续时间和体温过低呈剂量相关的降低,而不改变戊巴比妥在脑或血浆中的分布。给予与组胺结构相关的化合物不会改变自发活动或缩短麻醉持续时间。虽然用H2组胺拮抗剂西咪替丁预处理无效,但发现H1组胺拮抗剂可消除组胺诱导的觉醒。给予能显著减弱苯丙胺引起的自发运动活动增加的剂量的氟哌啶醇,不会改变组胺诱导的多动。同样,阿托品也不会显著改变组胺诱导的觉醒。这些数据支持组胺可能在调节行为觉醒中发挥作用的假说。

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