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大麻素对CB1基因敲除小鼠和CD1小鼠情境性条件性恐惧的影响。

The effects of cannabinoids on contextual conditioned fear in CB1 knockout and CD1 mice.

作者信息

Mikics Eva, Dombi Timea, Barsvári Beáta, Varga Balázs, Ledent Catherine, Freund Tamás F, Haller József

机构信息

Institute of Experimental Medicine, Budapest, Hungary.

出版信息

Behav Pharmacol. 2006 May;17(3):223-30. doi: 10.1097/00008877-200605000-00003.

DOI:10.1097/00008877-200605000-00003
PMID:16572000
Abstract

We studied the effects of cannabinoids on contextual conditioned fear responses. CB1 knockout and wild-type (CD1) mice were exposed to a brief session of electric shocks, and their behavior was studied in the same context 24 h later. In wild-type mice, shock exposure increased freezing and resting, and decreased locomotion and exploration. The genetic disruption of the CB1 receptor abolished the conditioned fear response. The CB1 antagonist AM-251 reduced the peak of the conditioned fear response when applied 30 min before behavioral testing (i.e. 24 h after shocks) in CD1 (wild-type) mice. The cannabinoid agonist WIN-55,212-2 markedly increased the conditioned fear response in CD1 mice, the effect of which was potently antagonized by AM-251. Thus, cannabinoid receptor activation appears to strongly promote the expression of contextual conditioned fear. In earlier experiments, cannabinoids did not interfere with the expression of cue-induced conditioned fear but strongly promoted its extinction. Considering the primordial role of the amygdala in simple associative learning (e.g. in cue-induced fear) and the role of the hippocampus in learning more complex stimulus relationships (e.g. in contextual fear), the present and earlier findings are not necessarily contradictory, but suggest that cannabinoid signaling plays different roles in the two structures. Data are interpreted in terms of the potential involvement of cannabinoids in trauma-induced behavioral changes.

摘要

我们研究了大麻素对情境性条件恐惧反应的影响。将CB1基因敲除小鼠和野生型(CD1)小鼠暴露于短暂的电击刺激下,并在24小时后于相同情境下研究它们的行为。在野生型小鼠中,电击暴露增加了僵住和静息行为,减少了运动和探索行为。CB1受体的基因破坏消除了条件恐惧反应。在行为测试前30分钟(即电击后24小时)给CD1(野生型)小鼠施用CB1拮抗剂AM - 251,可降低条件恐惧反应的峰值。大麻素激动剂WIN - 55,212 - 2显著增加了CD1小鼠的条件恐惧反应,而AM - 251可有效拮抗其作用。因此,大麻素受体激活似乎强烈促进情境性条件恐惧的表达。在早期实验中,大麻素并未干扰线索诱导的条件恐惧的表达,但强烈促进了其消退。考虑到杏仁核在简单联想学习(如线索诱导的恐惧)中的首要作用以及海马体在学习更复杂刺激关系(如情境恐惧)中的作用,目前和早期的研究结果不一定相互矛盾,而是表明大麻素信号在这两个结构中发挥着不同的作用。数据是根据大麻素可能参与创伤诱导的行为变化来解释的。

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