Suppr超能文献

青春期大鼠社交行为的双向大麻素调节

Bidirectional cannabinoid modulation of social behavior in adolescent rats.

作者信息

Trezza Viviana, Vanderschuren Louk J M J

机构信息

Rudolf Magnus Institute of Neuroscience, Department of Neuroscience and Pharmacology, University Medical Center Utrecht, Universiteitsweg 100, 3584 CG Utrecht, The Netherlands.

出版信息

Psychopharmacology (Berl). 2008 Apr;197(2):217-27. doi: 10.1007/s00213-007-1025-3. Epub 2007 Dec 6.

Abstract

RATIONALE

Marijuana use in adolescents is a highly social activity, and interacting endocannabinoid and opioid systems may modulate social reward. However, cannabinoid exposure has been reported to reduce social behavior.

OBJECTIVES

The aim of this study was to elucidate the mechanisms underlying the paradoxical relationship between cannabinoid exposure and sociability.

MATERIALS AND METHODS

We investigated the effect of cannabinoid agonists with a different mechanism of action on social play behavior in adolescent rats. In addition, we examined whether endocannabinoid neurotransmission interacts with opioid and dopaminergic neurotransmission in the modulation of social play behavior.

RESULTS

The direct CB1 cannabinoid receptor agonist WIN55,212-2 reduced social play. However, the indirect cannabinoid agonist URB597, which inhibits the hydrolysis of the endocannabinoid anandamide, enhanced social play. This effect of URB597 depended upon stimulation of opioid and dopamine receptors. The well-known stimulatory effect of morphine on social play was attenuated by the CB1 cannabinoid receptor antagonist SR141716A, but independent of dopamine receptor stimulation. Combined treatment with ineffective doses of URB597 and morphine increased social play.

CONCLUSIONS

Cannabinoid neurotransmission can both enhance and inhibit social interaction in adolescent rats depending on how the endocannabinoid system is stimulated. Activation of cannabinoid receptors throughout the brain, which occurs during cannabis use, inhibits sociability. In contrast, on-demand release of endocannabinoids facilitates social interaction, which is magnified by indirect cannabinoid agonists through an interaction with opioid and dopaminergic neurotransmission. These results shed light on the paradoxical relationship between cannabis exposure and sociability and suggest that endocannabinoid degradation inhibitors hold promise for the treatment of social dysfunctions.

摘要

理论依据

青少年使用大麻是一种高度社会化的活动,内源性大麻素系统与阿片类系统的相互作用可能会调节社会奖赏。然而,据报道大麻素暴露会减少社交行为。

目的

本研究旨在阐明大麻素暴露与社交性之间矛盾关系背后的机制。

材料与方法

我们研究了具有不同作用机制的大麻素激动剂对青春期大鼠社交玩耍行为的影响。此外,我们还研究了内源性大麻素神经传递在调节社交玩耍行为中是否与阿片类和多巴胺能神经传递相互作用。

结果

直接的CB1大麻素受体激动剂WIN55,212-2减少了社交玩耍。然而,间接大麻素激动剂URB597可抑制内源性大麻素花生四烯乙醇胺的水解,增强了社交玩耍。URB597的这种作用取决于阿片类和多巴胺受体的刺激。吗啡对社交玩耍的众所周知的刺激作用被CB1大麻素受体拮抗剂SR141716A减弱,但与多巴胺受体刺激无关。无效剂量的URB597和吗啡联合治疗增加了社交玩耍。

结论

大麻素神经传递在青春期大鼠中既可以增强也可以抑制社交互动,这取决于内源性大麻素系统如何被刺激。在使用大麻期间大脑中发生的大麻素受体激活会抑制社交性。相比之下,内源性大麻素的按需释放促进社交互动,间接大麻素激动剂通过与阿片类和多巴胺能神经传递的相互作用放大了这种促进作用。这些结果揭示了大麻暴露与社交性之间的矛盾关系,并表明内源性大麻素降解抑制剂有望用于治疗社交功能障碍。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验