Kott J M, Mooney-Leber S M, Li J, Brummelte S
Department of Psychology, Wayne State University, Detroit, MI, USA.
Karmanos Cancer Institute, School of Medicine, Wayne State University, Detroit, MI, USA.
Behav Brain Res. 2018 Aug 1;348:101-114. doi: 10.1016/j.bbr.2018.04.006. Epub 2018 Apr 6.
Many women who take antidepressant medications become pregnant while taking their medication; however, the impact of depression and antidepressant medication on fetal development is not well understood. This study used a translational animal model of maternal depression to investigate the consequences of discontinuing antidepressant medication during pregnancy. First, rats received corticosterone (CORT; 40 mg/kg, s.c.) or vehicle to induce a depressive-like phenotype. After 16 days of treatment with CORT or vehicle, animals were treated with sertraline (a selective serotonin reuptake inhibitor, SSRI; 20 mg/kg) or vehicle via gavage. Following 21 days of CORT or oil treatment, rats were mated. One group receiving sertraline was discontinued from treatment on gestational day 16, and another group continued sertraline treatment throughout pregnancy to assess the effects of discontinuation. After weaning, dams were sacrificed via perfusion to investigate neurogenesis. As intended, CORT administration created a depressive-like phenotype with increased immobility in the Forced Swim Test and reduced body weight. Interestingly, sertraline treatment could not rescue these altered features. Pre-conceptional CORT exposure resulted in smaller litters and CORT dams that received sertraline until the end of gestation spent more time off of the nest compared to CORT dams that received vehicle or discontinued sertraline during gestation. There was no difference in hippocampal neurogenesis between any of the groups. Our results suggest that treatment with antidepressants may have different effects in healthy or depressed dams, however, we need more research to investigate the detailed and long-term effects of maternal depression and its treatment in translational animal models.
许多服用抗抑郁药物的女性在服药期间怀孕;然而,抑郁症和抗抑郁药物对胎儿发育的影响尚未得到充分了解。本研究使用了一种母体抑郁症的转化动物模型来研究孕期停用抗抑郁药物的后果。首先,给大鼠注射皮质酮(CORT;40mg/kg,皮下注射)或赋形剂以诱导出类似抑郁的表型。在用CORT或赋形剂治疗16天后,通过灌胃给动物服用舍曲林(一种选择性5-羟色胺再摄取抑制剂,SSRI;20mg/kg)或赋形剂。在进行21天的CORT或油处理后,让大鼠交配。一组接受舍曲林治疗的大鼠在妊娠第16天停止治疗,另一组在整个孕期持续接受舍曲林治疗以评估停药的影响。断奶后,通过灌注处死母鼠以研究神经发生情况。正如预期的那样,注射CORT产生了一种类似抑郁的表型,在强迫游泳试验中不动时间增加且体重减轻。有趣的是,舍曲林治疗并不能挽救这些改变的特征。孕前暴露于CORT导致产仔数减少,与在孕期接受赋形剂或停用舍曲林的CORT母鼠相比,接受舍曲林直至妊娠结束的CORT母鼠离开巢穴的时间更长。各组之间海马神经发生没有差异。我们的结果表明,抗抑郁药物治疗在健康或抑郁的母鼠中可能有不同的效果,然而,我们需要更多的研究来调查母体抑郁症及其治疗在转化动物模型中的详细和长期影响。