Maciag Dorota, Williams Lashondra, Coppinger David, Paul Ian A
Department of Psychiatry & Human Behavior, University of Mississippi Medical Center, Jackson, MS 39216-4505, USA.
Eur J Pharmacol. 2006 Feb 27;532(3):265-9. doi: 10.1016/j.ejphar.2005.12.081. Epub 2006 Feb 14.
Neonatal exposure to antidepressants, including selective serotonin reuptake inhibitors such as citalopram, induces behavioral disturbances which persist in mature rats. These disturbances have been proposed to model the symptoms of endogenous depression. However, to date there is scant evidence for the predictive validity of any of these behaviors in response to adult antidepressant treatments. In order to directly assess the predictive validity of the early antidepressant exposure paradigm, the present study examined whether the behavioral abnormalities observed in adult animals exposed as neonates to citalopram can be reversed by adult antidepressant treatment with the prototypic antidepressant, imipramine. As noted earlier, neonatal citalopram exposure robustly increased locomotor activity and impaired male sexual behavior in adult rats. These behavioral changes were reversed following chronic adult imipramine treatment. No such reversal was observed in handled, saline treated rats. The present data support the hypothesis that some of the lasting behavioral abnormalities induced by early antidepressant exposure are sensitive to clinically relevant antidepressant treatments thus adding a measure of predictive validity to this paradigm as a model of these depressive symptoms.
新生儿接触抗抑郁药,包括如西酞普兰等选择性5-羟色胺再摄取抑制剂,会引发行为障碍,且这些障碍在成年大鼠中持续存在。有人提出这些障碍可作为内源性抑郁症症状的模型。然而,迄今为止,几乎没有证据表明这些行为中的任何一种对于成年抗抑郁药治疗具有预测效度。为了直接评估早期抗抑郁药暴露范式的预测效度,本研究考察了成年后用典型抗抑郁药丙咪嗪进行抗抑郁治疗,是否能逆转新生期接触西酞普兰的成年动物所观察到的行为异常。如前所述,新生期接触西酞普兰会显著增加成年大鼠的运动活性并损害其性行为。成年大鼠经慢性丙咪嗪治疗后,这些行为变化得到了逆转。在接受过抓握处理、给予生理盐水的大鼠中未观察到这种逆转。目前的数据支持这样一种假说,即早期抗抑郁药暴露所诱发的一些持续性行为异常对临床相关的抗抑郁治疗敏感,因此为该范式作为这些抑郁症状的模型增加了一定程度的预测效度。