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反复不可预测应激降低小鼠对糖精的偏好及其被丙咪嗪预防的作用

Reduction in preference for saccharin by repeated unpredictable stress in mice and its prevention by imipramine.

作者信息

Harkin Andrew, Houlihan Diarmaid D, Kelly John P

机构信息

Department of Pharmacology, National University of Ireland, Galway.

出版信息

J Psychopharmacol. 2002 Jun;16(2):115-23. doi: 10.1177/026988110201600201.

Abstract

The present study set out to establish the chronic mild stress (CMS) animal model of depression in male CD-1 mice, a commonly used mouse strain. Mice were exposed to a series of mild stressors (e.g. soiled bedding, paired housing, cage tilt, white noise) presented in a continuous unpredictable fashion. Intermittently, CMS was discontinued and the mice were presented with both water and a palatable saccharin solution (0.1% w/v) in a two-bottle choice test overnight (15 h). Repeated exposure of these mice to the stressors led to a reduction in preference for the saccharin solution. This change in preference was attributed to an increase in the consumption of water rather than a decrease in the consumption of saccharin solution. Over time and with extensive testing, CMS no longer affected performance in the two-bottle saccharin preference test. Treatment with the tricyclic antidepressant imipramine (20 mg/kg i.p., once daily) had a varied effect on the CMS-induced change in preference for saccharin, dependent on the timing of initiation of imipramine treatment. In the first instance, following 5 weeks of CMS where a reduction in saccharin preference was established, treatment with imipramine for a further 5 weeks maintained the stress-induced deficit in saccharin preference. However, using a different approach, pre-treatment with imipramine once daily for 2 weeks, prior to onset of CMS, and co-treatment thereafter, attenuated CMS-induced changes in saccharin preference. Finally, when imipramine treatment was scheduled to begin with the CMS procedure, imipramine failed to prevent the CMS-induced reductions in saccharin preference. Changes in behaviour observed after exposure to CMS may be linked to a stress-induced deterioration of the sensitivity of the mice to a rewarding stimulus. Treatment with imipramine can reduce these behavioural changes but is only effective when given repeatedly prior to onset of CMS.

摘要

本研究旨在建立雄性CD-1小鼠(一种常用的小鼠品系)的慢性轻度应激(CMS)抑郁症动物模型。小鼠连续且不可预测地暴露于一系列轻度应激源(如脏垫料、配对饲养、笼子倾斜、白噪声)。间歇性地,停止CMS,在两瓶装选择试验中让小鼠过夜(15小时)同时饮用普通水和可口的糖精溶液(0.1%w/v)。这些小鼠反复暴露于应激源导致对糖精溶液的偏好降低。这种偏好变化归因于水消耗量的增加而非糖精溶液消耗量的减少。随着时间推移和广泛测试,CMS不再影响两瓶装糖精偏好试验中的表现。三环类抗抑郁药丙咪嗪(20mg/kg腹腔注射,每日一次)治疗对CMS诱导的糖精偏好变化有不同影响,这取决于丙咪嗪治疗开始的时间。首先,在建立了糖精偏好降低的CMS 5周后,再用丙咪嗪治疗5周维持了应激诱导的糖精偏好缺陷。然而,采用不同方法,在CMS开始前每日一次用丙咪嗪预处理2周,随后联合治疗,减弱了CMS诱导的糖精偏好变化。最后,当丙咪嗪治疗计划与CMS程序同时开始时,丙咪嗪未能预防CMS诱导的糖精偏好降低。暴露于CMS后观察到的行为变化可能与应激诱导的小鼠对奖励刺激的敏感性恶化有关。丙咪嗪治疗可减少这些行为变化,但仅在CMS开始前反复给药时有效。

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