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大麻二酚在小鼠体内的抗抑郁样作用:可能涉及 5-HT1A 受体。

Antidepressant-like effects of cannabidiol in mice: possible involvement of 5-HT1A receptors.

机构信息

Department of Pharmacology, School of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.

出版信息

Br J Pharmacol. 2010 Jan;159(1):122-8. doi: 10.1111/j.1476-5381.2009.00521.x. Epub 2009 Dec 4.

Abstract

BACKGROUND AND PURPOSE

Cannabidiol (CBD) is a non-psychotomimetic compound from Cannabis sativa that induces anxiolytic- and antipsychotic-like effects in animal models. Effects of CBD may be mediated by the activation of 5-HT(1A) receptors. As 5-HT(1A) receptor activation may induce antidepressant-like effects, the aim of this work was to test the hypothesis that CBD would have antidepressant-like activity in mice as assessed by the forced swimming test. We also investigated if these responses depended on the activation of 5-HT(1A) receptors and on hippocampal expression of brain-derived neurotrophic factor (BDNF).

EXPERIMENTAL APPROACH

Male Swiss mice were given (i.p.) CBD (3, 10, 30, 100 mgkg(-1)), imipramine (30 mgkg(-1)) or vehicle and were submitted to the forced swimming test or to an open field arena, 30 min later. An additional group received WAY100635 (0.1 mgkg(-1), i.p.), a 5-HT(1A) receptor antagonist, before CBD (30 mgkg(-1)) and assessment by the forced swimming test. BDNF protein levels were measured in the hippocampus of another group of mice treated with CBD (30 mg*kg(-1)) and submitted to the forced swimming test.

KEY RESULTS

CBD (30 mgkg(-1)) treatment reduced immobility time in the forced swimming test, as did the prototype antidepressant imipramine, without changing exploratory behaviour in the open field arena. WAY100635 pretreatment blocked CBD-induced effect in the forced swimming test. CBD (30 mgkg(-1)) treatment did not change hippocampal BDNF levels.

CONCLUSION AND IMPLICATIONS

CBD induces antidepressant-like effects comparable to those of imipramine. These effects of CBD were probably mediated by activation of 5-HT(1A) receptors.

摘要

背景和目的

大麻素(CBD)是一种非致幻化合物,来自大麻植物,在动物模型中诱导出抗焦虑和抗精神病样效应。CBD 的作用可能是通过激活 5-HT(1A)受体介导的。由于 5-HT(1A)受体的激活可能会诱导抗抑郁样作用,因此本工作的目的是通过强迫游泳试验来检验 CBD 会在小鼠中产生抗抑郁样活性的假说。我们还研究了这些反应是否依赖于 5-HT(1A)受体的激活以及海马脑源性神经营养因子(BDNF)的表达。

实验方法

雄性瑞士小鼠给予(ip)CBD(3、10、30、100 mgkg(-1))、丙咪嗪(30 mgkg(-1))或载体,并在 30 分钟后进行强迫游泳试验或开放场试验。另一组在给予 CBD(30 mgkg(-1))之前接受 WAY100635(0.1 mgkg(-1),ip),一种 5-HT(1A)受体拮抗剂,并通过强迫游泳试验进行评估。另一组小鼠给予 CBD(30 mg*kg(-1))并进行强迫游泳试验,测量其海马体中的 BDNF 蛋白水平。

主要结果

CBD(30 mgkg(-1))治疗可减少强迫游泳试验中的不动时间,与原型抗抑郁药丙咪嗪一样,而不改变开放场试验中的探索行为。WAY100635 预处理可阻断 CBD 在强迫游泳试验中的作用。CBD(30 mgkg(-1))治疗并未改变海马体 BDNF 水平。

结论和意义

CBD 诱导出与丙咪嗪相当的抗抑郁样作用。CBD 的这些作用可能是通过激活 5-HT(1A)受体介导的。

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