Neurodevelopmental Changes in Offspring Prenatally Exposed to Opioids in Human Children and Rodent Models: A Review

Eunice B Quagraine
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Abstract

The number of infants born to opioid-dependent pregnant women in North America is a growing problem. Studies that focus on the long-term effects of neurodevelopmental changes of prenatal opioid exposure in human infants are however limited. The use of rodent models to evaluate these changes may provide some insight. This review focuses on studies of rodent models exposed to opioids such as morphine, heroin, oxycodone, buprenorphine, methadone, and l-α-acetylmethadol in uteroand briefly discusses the neural and behavioural effects in human children. Most of the rodent studies reported the following neural effects: increases in caspase-3 and Bax/Bcl-2 ratio, altered NMDA activity, and decreases in BDNF expression in the offspring prenatally exposed to opioids. In addition, they showed decreases in synaptic plasticity, LTP, LTD, dendritic length, and dendritic branch number. The exposed rodent offspring were more inclined to perform poorly in the behavioural tests. Likewise, some of the human studies reported a significant difference between the exposed group and the control; however, other studies reported insignificant or no significant differences after correcting for covariates. Most of the studies suggest an impairment in learning and memory in the rodent offspring and deficits in behaviour and cognition in human children; however, this was not always the case. It is still not clear whether the effects of prenatal opioid exposure are due to the opioid itself being the prime factor, as various factors may also contribute to the results. Further studies of the effects of early opioid exposure on neurodevelopment in the offspring are required.
人类儿童和啮齿类动物模型中产前暴露于阿片类药物的后代神经发育变化:综述
在北美,阿片类药物依赖孕妇所生婴儿的数量是一个日益严重的问题。然而,关于产前阿片类药物暴露对人类婴儿神经发育变化的长期影响的研究是有限的。使用啮齿动物模型来评估这些变化可能会提供一些见解。本文综述了吗啡、海洛因、羟考酮、丁丙诺啡、美沙酮和l-α-乙酰美沙醇等阿片类药物在子宫内暴露的啮齿动物模型的研究,并简要讨论了这些药物对人类儿童的神经和行为影响。大多数啮齿动物研究报告了以下神经效应:caspase-3和Bax/Bcl-2比值升高,NMDA活性改变,BDNF表达降低。此外,突触可塑性、LTP、LTD、树突长度和树突分支数均下降。暴露的啮齿动物后代在行为测试中表现更差。同样,一些人体研究报告了暴露组和对照组之间的显著差异;然而,其他研究在校正协变量后报告不显著或无显著差异。大多数研究表明啮齿动物的后代在学习和记忆方面有缺陷,人类儿童在行为和认知方面有缺陷;然而,情况并非总是如此。目前尚不清楚产前阿片类药物暴露的影响是否由于阿片类药物本身是主要因素,因为各种因素也可能导致结果。需要进一步研究早期阿片类药物暴露对后代神经发育的影响。
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