选择性血清素再摄取抑制剂停药对小鼠焦虑样行为的影响

H. Collins, R. Pinacho, D. Ozdemir, D. Bannerman, T. Sharp
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引用次数: 5

摘要

背景:突然停止选择性5 -羟色胺再摄取抑制剂(SSRI)治疗与停药综合征相关,以许多致残症状为典型,包括焦虑。令人惊讶的是,人们对停用SSRI对动物行为的影响知之甚少。目的:在此,系统地研究了SSRI停药对小鼠焦虑样行为的影响。方法:实验采用三组实验设计,包括生理盐水、持续SSRI和停用SSRI。在SSRI停药后的第2天,在5天的时间里,使用升高加迷宫(EPM)和其他焦虑测试对小鼠进行评估。结果:一项探索性实验发现,在雄性小鼠中,停止服用帕罗西汀(12天)与张开手臂探索的减少和总行走距离的减少有关,但雌性小鼠没有。后续研究证实,帕罗西汀(12天)和西酞普兰(12天)对雄性小鼠EPM有停药作用。继续服用帕罗西汀(而不是西酞普兰)的小鼠也显示出张开臂探索减少,但这与停药的影响是分离的。对帕罗西汀的停药反应在治疗28天后没有增强,但在治疗7天后没有增强。在治疗停止后3-5天进行的其他焦虑和恐惧学习测试中,没有发现停药反应。最后,停药对EPM的影响通常与测试中运动能力下降有关。然而,单独的运动测试暗示焦虑引起的行为抑制,而不是运动活动的普遍减少。结论:总体而言,本研究为小鼠停止SSRI治疗后的短期行为停止反应提供了证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of selective serotonin reuptake inhibitor discontinuation on anxiety-like behaviours in mice
Background: Abrupt cessation of therapy with a selective serotonin reuptake inhibitor (SSRI) is associated with a discontinuation syndrome, typified by numerous disabling symptoms, including anxiety. Surprisingly, little is known of the behavioural effect of SSRI discontinuation in animals. Aim: Here, the effect of SSRI discontinuation on anxiety-like behaviour was systematically investigated in mice. Methods: Experiments were based on a three-arm experimental design comprising saline, continued SSRI and discontinued SSRI. Mice were assessed 2 days after SSRI discontinuation over a 5-day period using the elevated plus maze (EPM) and other anxiety tests. Results: An exploratory experiment found cessation of paroxetine (12 days) was associated with decreased open-arm exploration and reduced total distance travelled, in male but not female mice. Follow-up studies confirmed a discontinuation effect on the EPM in male mice after paroxetine (12 days) and also citalopram (12 days). Mice receiving continued paroxetine (but not citalopram) also showed decreased open-arm exploration but this was dissociable from the effects of discontinuation. The discontinuation response to paroxetine did not strengthen after 28 days of treatment but was absent after 7 days of treatment. A discontinuation response was not discernible in other anxiety and fear-learning tests applied 3–5 days after treatment cessation. Finally, discontinuation effects on the EPM were typically associated with decreased locomotion on the test. However, separate locomotor testing implicated anxiety-provoked behavioural inhibition rather than a general reduction in motor activity. Conclusion: Overall, this study provides evidence for a short-lasting behavioural discontinuation response to cessation of SSRI treatment in mice.
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