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大麻素与应激:HU - 210对急性应激小鼠焦虑行为测试的影响

Cannabinoids & Stress: impact of HU-210 on behavioral tests of anxiety in acutely stressed mice.

作者信息

Kinden Renee, Zhang Xia

机构信息

University of Ottawa's Institute of Mental Health Research at the Royal Ottawa, Departments of Psychiatry and Cellular & Molecular Medicine, Ottawa, K1Z 7K4 Canada.

University of Ottawa's Institute of Mental Health Research at the Royal Ottawa, Departments of Psychiatry and Cellular & Molecular Medicine, Ottawa, K1Z 7K4 Canada.

出版信息

Behav Brain Res. 2015 May 1;284:225-30. doi: 10.1016/j.bbr.2015.02.025. Epub 2015 Feb 20.

Abstract

Anxiety disorders are one of the most prevalent classes of mental disorders affecting the general population, but current treatment strategies are restricted by their limited efficacy and side effect profiles. Although the cannabinoid system is speculated to be a key player in the modulation of stress responses and emotionality, the vast majority of current research initiatives had not incorporated stress exposure into their experimental designs. This study was the first to investigate the impact of exogenous cannabinoid administration in an acutely stressed mouse model, where CD1 mice were pre-treated with HU-210, a potent CB1R agonist, prior to acute stress exposure and subsequent behavioral testing. Exogenous cannabinoid administration induced distinct behavioral phenotypes in stressed and unstressed mice. While low doses of HU-210 were anxiolytic in unstressed subjects, this effect was abolished when mice were exposed to an acute stressor. The administration of higher HU-210 doses in combination with acute stress exposure led to severe locomotor deficits that were not previously observed at the same dose in unstressed subjects. These findings suggest that exogenous cannabinoids and acute stress act synergistically in an anxiogenic manner. This study underlies the importance of including stress exposure into future anxiety-cannabinoid research due to the differential impact of cannabinoid administration on stressed and unstressed subjects.

摘要

焦虑症是影响普通人群的最常见精神障碍类型之一,但目前的治疗策略因其有限的疗效和副作用而受到限制。尽管大麻素系统被推测在调节应激反应和情绪方面起关键作用,但目前绝大多数研究项目在实验设计中并未纳入应激暴露因素。本研究首次在急性应激小鼠模型中研究外源性大麻素给药的影响,其中在急性应激暴露和随后的行为测试之前,对CD1小鼠预先给予强效CB1R激动剂HU-210。外源性大麻素给药在应激和非应激小鼠中诱导出不同的行为表型。虽然低剂量的HU-210在非应激小鼠中具有抗焦虑作用,但当小鼠暴露于急性应激源时,这种作用就会消失。高剂量HU-210与急性应激暴露联合给药会导致严重的运动缺陷,而在相同剂量下,非应激小鼠中并未观察到这种情况。这些发现表明,外源性大麻素和急性应激以一种致焦虑的方式协同作用。由于大麻素给药对应激和非应激小鼠有不同影响,本研究强调了在未来焦虑症与大麻素研究中纳入应激暴露的重要性。

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