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应用于大细胞基底核区域的H1和H2组胺阻滞剂氯苯那敏和雷尼替丁可调节焦虑和强化相关过程。

The H1- and H2-histamine blockers chlorpheniramine and ranitidine applied to the nucleus basalis magnocellularis region modulate anxiety and reinforcement related processes.

作者信息

Privou C, Knoche A, Hasenöhrl R U, Huston J P

机构信息

Institute of Physiological Psychology I and Center for Biological and Medical Research, University of Düsseldorf, Germany.

出版信息

Neuropharmacology. 1998 Aug;37(8):1019-32. doi: 10.1016/s0028-3908(98)00087-2.

DOI:10.1016/s0028-3908(98)00087-2
PMID:9833631
Abstract

This study examined the effects of the H1-antagonist chlorpheniramine and the H2-antagonist ranitidine on reinforcement and anxiety-parameters following unilateral injection into the vicinity of the nucleus basalis magnocellularis (NBM). In Experiment 1, rats with chronically implanted cannulae were injected with chlorpheniramine or ranitidine (each at doses of 0.1, 1, 10 and 20 microg) and were placed into one of four restricted quadrants of a circular open field (closed corral) for a single conditioning trial. During the test for conditioned corral preference, when provided a choice between the four quadrants, only those rats injected with 10 or 20 microg chlorpheniramine spent more time in the treatment corral, indicative of a positively reinforcing action. None of the other doses of chlorpheniramine or of the H2-antagonist influenced rats' preference behavior. In Experiment 2, the elevated plus-maze (EPM) was used to gauge possible anxiolytic or anxiogenic effects of intra-basalis injection of chlorpheniramine or ranitidine (each at doses of 0.1, 1, 10 and 20 microg). A single injection of chlorpheniramine at 0.1 or 20 microg as well as ranitidine at 20 microg was found to exert anxiolytic-like effects in the EPM. Both compounds elevated the time spent on the open arms and increased scanning over the edge of an open arm. None of the other doses of the H1- and H2-antagonist influenced rats' behavior in the EPM. In sum, these findings show that H1- and H2-receptor antagonists differentially modulate reinforcement and fear-related processes in the NBM and thus, provide the first evidence for a behavioral relevance for the histaminergic innervation of this brain site.

摘要

本研究检测了H1拮抗剂氯苯那敏和H2拮抗剂雷尼替丁单侧注射至大细胞基底核(NBM)附近后对强化作用和焦虑参数的影响。在实验1中,给长期植入套管的大鼠注射氯苯那敏或雷尼替丁(剂量分别为0.1、1、10和20微克),并将其置于圆形旷场(封闭畜栏)的四个受限象限之一进行单次条件试验。在条件性畜栏偏好测试中,当在四个象限之间进行选择时,只有注射10或20微克氯苯那敏的大鼠在处理畜栏中停留的时间更长,表明有正向强化作用。氯苯那敏的其他剂量或H2拮抗剂均未影响大鼠的偏好行为。在实验2中,采用高架十字迷宫(EPM)来评估基底核内注射氯苯那敏或雷尼替丁(剂量分别为0.1、1、10和20微克)可能产生的抗焦虑或致焦虑作用。发现单次注射0.1或20微克氯苯那敏以及20微克雷尼替丁在EPM中具有抗焦虑样作用。两种化合物均增加了在开放臂上停留的时间,并增加了在开放臂边缘的扫视。H1和H2拮抗剂的其他剂量均未影响大鼠在EPM中的行为。总之,这些发现表明,H1和H2受体拮抗剂对NBM中的强化作用和恐惧相关过程具有不同的调节作用,因此,为该脑区组胺能神经支配的行为相关性提供了首个证据。

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