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低浓度的花生四烯酸乙醇胺通过激活 CB1 受体促进雄性大鼠的性行为。

Low anandamide doses facilitate male rat sexual behaviour through the activation of CB1 receptors.

机构信息

Departamento de Farmacobiología, Cinvestav-Sede Sur, Calzada de los Tenorios 235, Col. Granjas Coapa, Delegación Tlalpan, 14330, México D.F, México.

出版信息

Psychopharmacology (Berl). 2014 Oct;231(20):4071-80. doi: 10.1007/s00213-014-3547-9. Epub 2014 Mar 27.

Abstract

RATIONALE

Endocannabinoids (eCN) exert biphasic effects on several behaviours; however, they have only been reported to inhibit male sexual behaviour. eCN, the endogenous ligands for CB1 receptors, are released in response to neuronal stimulation and regulate the functioning of the mesocorticolimbic system (MCL), which is activated by male sexual behaviour. We hypothesised that eCN might exert biphasic effects on male rat copulatory behaviour and be released during copulation to satiation as a result of the repeated activation of the MCL system.

OBJECTIVES

The study was conducted to determine if the eCN anandamide exerts biphasic effects on sexual behaviour expression of sexually experienced and sexually satiated male rats and to establish the possible participation of eCN in the sexual satiation phenomenon.

METHODS

The eCN anandamide and the CB1 receptor antagonist AM251 were systemically administered to sexually experienced or sexually satiated rats and their effects on copulatory behaviour analysed.

RESULTS

Low anandamide doses facilitated sexual behaviour expression in sexually experienced and in sexually satiated rats by acting at CB1 receptors. AM251 blocked the establishment of the sexual inhibition that characterises sexual satiation, but did not reverse it once established.

CONCLUSIONS

Anandamide exerts dose-based biphasic effects on copulatory behaviour of sexually experienced male rats and facilitates sexual behaviour expression of sexually satiated animals at low doses. eCN participate in the establishment, but not in the maintenance of the sexual inhibitory state that characterises the sexual satiation phenomenon.

摘要

原理

内源性大麻素 (eCN) 对多种行为具有双相作用;然而,它们仅被报道抑制雄性性行为。eCN 是 CB1 受体的内源性配体,响应神经元刺激而释放,并调节中皮质边缘系统 (MCL) 的功能,该系统被雄性性行为激活。我们假设 eCN 可能对雄性大鼠交配行为产生双相作用,并在交配中由于 MCL 系统的反复激活而在饱足时释放。

目的

本研究旨在确定内源性大麻素大麻素酰胺是否对有性经验和有性饱足的雄性大鼠的性行为表达产生双相作用,并确定内源性大麻素在性饱足现象中的可能参与。

方法

系统给予有性经验或有性饱足的大鼠内源性大麻素大麻素酰胺和 CB1 受体拮抗剂 AM251,并分析其对交配行为的影响。

结果

低剂量的大麻素酰胺通过作用于 CB1 受体促进有性经验和有性饱足的大鼠的性行为表达。AM251 阻断了特征为性饱足的性抑制的建立,但一旦建立就不能逆转。

结论

大麻素酰胺对有性经验的雄性大鼠的交配行为产生基于剂量的双相作用,并在低剂量下促进有性饱足动物的性行为表达。内源性大麻素参与建立,但不参与特征为性饱足现象的性抑制状态的维持。

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