Odegaard Katherine E, Schaal Victoria L, Clark Alexander R, Koul Sneh, Sankarasubramanian Jagadesan, Xia Zhiqiu, Mellon Melissa, Uberti Mariano, Liu Yutong, Stothert Andrew, Van Hook Matthew, Wang Hanjun, Guda Chittibabu, Lisco Steven J, Pendyala Gurudutt, Yelamanchili Sowmya V
Department of Anesthesiology, University of Nebraska Medical Center, Omaha, NE, United States.
Department of Genetics, Cell Biology & Anatomy, University of Nebraska Medical Center, Omaha, NE, United States.
Front Cell Dev Biol. 2021 Jan 7;8:619199. doi: 10.3389/fcell.2020.619199. eCollection 2020.
Increased risk of oxycodone (oxy) dependency during pregnancy has been associated with altered behaviors and cognitive deficits in exposed offspring. However, a significant knowledge gap remains regarding the effect of and postnatal exposure on neurodevelopment and subsequent behavioral outcomes. Using a preclinical rodent model that mimics oxy exposure (IUO) and postnatally (PNO), we employed an integrative holistic systems biology approach encompassing proton magnetic resonance spectroscopy (H-MRS), electrophysiology, RNA-sequencing, and Von Frey pain testing to elucidate molecular and behavioral changes in the exposed offspring during early neurodevelopment as well as adulthood. H-MRS studies revealed significant changes in key brain metabolites in the exposed offspring that were corroborated with changes in synaptic currents. Transcriptomic analysis employing RNA-sequencing identified alterations in the expression of pivotal genes associated with synaptic transmission, neurodevelopment, mood disorders, and addiction in the treatment groups. Furthermore, Von Frey analysis revealed lower pain thresholds in both exposed groups. Given the increased use of opiates, understanding the persistent developmental effects of these drugs on children will delineate potential risks associated with opiate use beyond the direct effects in pregnant women.
孕期羟考酮(oxy)依赖风险增加与暴露后代的行为改变和认知缺陷有关。然而,关于孕期和产后暴露对神经发育及后续行为结果的影响,仍存在重大知识空白。我们使用一种模拟孕期(IUO)和产后(PNO)暴露于羟考酮的临床前啮齿动物模型,采用了一种综合的整体系统生物学方法,包括质子磁共振波谱(H-MRS)、电生理学、RNA测序和von Frey疼痛测试,以阐明暴露后代在早期神经发育以及成年期的分子和行为变化。H-MRS研究揭示了暴露后代关键脑代谢物的显著变化,这些变化与突触电流的变化相一致。采用RNA测序的转录组分析确定了治疗组中与突触传递、神经发育、情绪障碍和成瘾相关的关键基因表达的改变。此外,von Frey分析显示两个暴露组的疼痛阈值较低。鉴于阿片类药物的使用增加,了解这些药物对儿童持续的发育影响将明确与阿片类药物使用相关的潜在风险,而不仅仅是对孕妇的直接影响。