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孕期维拉佐酮暴露:通过BDNF/Bax-Bcl2/5-羟色胺介导机制对胚胎-胎儿发育、妊娠结局及胎儿神经毒性的影响

Vilazodone exposure during pregnancy: Effects on embryo-fetal development, pregnancy outcomes and fetal neurotoxicity by BDNF/Bax-Bcl2/5-HT mediated mechanisms.

作者信息

Agrawal Priyanka, Singh Pallavi, Singh K P

机构信息

Neurobiology Lab., Department of Zoology, University of Allahabad, Prayagraj, UP 211002, India.

出版信息

Neurotoxicology. 2024 Dec;105:280-292. doi: 10.1016/j.neuro.2024.10.012. Epub 2024 Nov 10.

Abstract

The high prevalence of major depressive disorder (MDD) among women of childbearing age necessitates careful consideration of antidepressant use during pregnancy. Although newer antidepressants, such as Vilazodone (VLZ), are preferred for their enhanced therapeutic profiles; however, their safety during pregnancy and long-term effects on offspring brains remain inadequately addressed. Therefore, this study aimed to investigate the reproductive and developmental neurotoxicity of VLZ given at equivalent therapeutic doses during gestation in a rat model. Pregnant Wistar dams were orally administered either with 1 mg/day or 2 mg/day of VLZ from gestation day (GD) 6-21. The dams were sacrificed at GD 21, and the placentas and fetuses were collected. Fetal brains were then subjected to neurohistopathological, neurochemical, and biochemical analysis. Prenatal exposure to VLZ at 2 mg/day resulted in significant maternal, reproductive, and embryo-fetal toxicity, characterized by reduced food intake, diminished weight gain in pregnant dams, and smaller litter sizes, along with decreased fetal and placental weights. These effects were associated with developmental neurotoxicity, which manifested as decreased fetal brain size and weight, a substantial reduction in neocortical layer thickness, brain-derived neurotrophic factor (BDNF) expression, serotonin, dopamine, and norepinephrine neurotransmitter levels (5-HT, DA, and NE), and increased apoptotic activity (Bax and Bcl-2 ratio) and acetylcholinesterase levels in the developing brain. Our findings indicate that prenatal VLZ exposure interfere with crucial brain development processes involving the BDNF/Bax-Bcl2/5-HT signalling pathways, leading to long-lasting neurodevelopmental impairments. This study is the first to document the adverse effects of VLZ on fetal brain development, highlighting the need for further research to assess the safety of VLZ use during pregnancy.

摘要

育龄女性中重度抑郁症(MDD)的高患病率使得孕期使用抗抑郁药需要谨慎考虑。尽管新型抗抑郁药,如维拉佐酮(VLZ),因其更好的治疗效果而更受青睐;然而,它们在孕期的安全性以及对后代大脑的长期影响仍未得到充分研究。因此,本研究旨在探讨在大鼠模型中,孕期给予等效治疗剂量的VLZ对生殖和发育的神经毒性。从妊娠第6天至第21天,对怀孕的Wistar母鼠每天口服1毫克或2毫克的VLZ。在妊娠第21天处死母鼠,收集胎盘和胎儿。然后对胎儿大脑进行神经组织病理学、神经化学和生化分析。孕期每天暴露于2毫克的VLZ会导致明显的母体、生殖和胚胎-胎儿毒性,表现为食物摄入量减少、怀孕母鼠体重增加减少、窝仔数减少,以及胎儿和胎盘重量减轻。这些影响与发育神经毒性有关,表现为胎儿脑大小和重量减小、新皮层厚度显著降低、脑源性神经营养因子(BDNF)表达减少、血清素、多巴胺和去甲肾上腺素神经递质水平(5-HT、DA和NE)降低,以及发育中的大脑中凋亡活性(Bax与Bcl-2比值)和乙酰胆碱酯酶水平升高。我们的研究结果表明,孕期暴露于VLZ会干扰涉及BDNF/Bax-Bcl2/5-HT信号通路的关键脑发育过程,导致长期的神经发育障碍。本研究首次记录了VLZ对胎儿脑发育的不良影响,强调需要进一步研究以评估孕期使用VLZ的安全性。

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