Blaine Brianna, Kamal Mushroor, Roberts Mizani, Schickling Brandon, Lauffer Marisol, Zhang Yuping, Bertolli Aimee, Weber Matthew A, Taylor Robert, Nadeem Sana, Patel Krushi, Teesch Lynn, Aldridge Georgina, Santillan Donna, Santillan Mark, Gumusoglu Serena
Iowa Neuroscience Institute, Iowa City, IA, USA.
University of Iowa Department of Obstetrics and Gynecology, Iowa City, IA, USA.
Mol Psychiatry. 2025 Jul 18. doi: 10.1038/s41380-025-03094-x.
Selective Serotonin Reuptake Inhibitors (SSRIs) are among the most common medications used for depression in postpartum and lactating people, who experience increased depression risk. However, there is a limited understanding of peripartum SSRI impacts on maternal neurobehavioral responses, and particularly those of sertraline, the most prescribed SSRI in United States (US) pregnancies. We administered C57Bl/6 females sertraline via a non-invasive, naturalistic approach (167 mg/L drinking water) from 2 weeks pre-conception through lactation (PND21) or for an equivalent duration in nonpregnant controls. We assessed behavior and molecular brain changes intrapartum and postpartum at ~1 year of age. Chronic sertraline reduced depressive- and anxiety-like behaviors. Pregnancy itself decreased anxiety-like and hedonic behaviors. RNA sequencing of maternal brain revealed only 52 differentially expressed genes (DEGs) in frontal cortex with sertraline. These DEGs over-represented functions related to immunity. In contrast, sertraline altered 962 targets in maternal hypothalamic paraventricular nucleus, with DEGs overrepresenting neurotransmission and neurodegeneration. We then discontinued sertraline and aged animals to approximately 1 year to test neurodegenerative phenotypes. Having one prior litter, regardless of peripartum sertraline, improved aged females' spatial learning and memory. Sertraline, regardless of postpartum status, improved working memory. Further, we found buffering of neurodegeneration-related gene network changes and increased excitatory synapse density in the hippocampus after peripartum sertraline. Peripartum sertraline alters maternal neurobiology and behavior in pregnancy and beyond, with long-term benefits to neurodegenerative processes. Pregnancy also exerts its own, lasting effects on learning and memory. These findings might be exploited in the future to abrogate neurodegenerative disease.
选择性5-羟色胺再摄取抑制剂(SSRIs)是产后和哺乳期人群中治疗抑郁症最常用的药物之一,这些人群患抑郁症的风险较高。然而,人们对围产期使用SSRI对母亲神经行为反应的影响了解有限,尤其是对舍曲林的影响了解更少,舍曲林是美国孕期最常用的SSRI。我们采用非侵入性、自然主义的方法(167mg/L饮用水),从受孕前2周开始,对C57Bl/6雌性小鼠给予舍曲林,直至哺乳期(出生后第21天),或在非怀孕对照组中给予相同时间的药物。我们在产后约1岁时评估了分娩期和产后的行为及大脑分子变化。长期服用舍曲林可减少抑郁和焦虑样行为。怀孕本身会降低焦虑样和享乐行为。对母体大脑进行RNA测序发现,使用舍曲林后,额叶皮质中只有52个差异表达基因(DEGs)。这些DEGs在与免疫相关的功能中过度表达。相比之下,舍曲林改变了母体下丘脑室旁核中的962个靶点,DEGs在神经传递和神经退行性变方面过度表达。然后,我们停止使用舍曲林,并将动物饲养至约1岁,以测试神经退行性表型。无论围产期是否使用舍曲林,有过一胎的老龄雌性小鼠的空间学习和记忆能力都会有所改善。无论产后状态如何,舍曲林都能改善工作记忆。此外,我们发现围产期使用舍曲林后,神经退行性相关基因网络变化得到缓冲,海马体中的兴奋性突触密度增加。围产期使用舍曲林会改变孕期及之后母体的神经生物学和行为,对神经退行性过程有长期益处。怀孕也会对学习和记忆产生自身的持久影响。这些发现未来可能会被用于消除神经退行性疾病。