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妊娠纳曲酮可改善胎儿乙醇暴露对产后乙醇行为和神经反应的增强作用。

Gestational naltrexone ameliorates fetal ethanol exposures enhancing effect on the postnatal behavioral and neural response to ethanol.

机构信息

Department of Psychiatry and Behavioral Sciences, State University of New York Upstate Medical University, 750 East Adams Street, Syracuse, NY 13210, USA.

出版信息

Exp Biol Med (Maywood). 2012 Oct;237(10):1197-208. doi: 10.1258/ebm.2012.012132. Epub 2012 Oct 8.

Abstract

The association between gestational exposure to ethanol and adolescent ethanol abuse is well established. Recent animal studies support the role of fetal ethanol experience-induced chemosensory plasticity as contributing to this observation. Previously, we established that fetal ethanol exposure, delivered through a dam's diet throughout gestation, tuned the neural response of the peripheral olfactory system of early postnatal rats to the odor of ethanol. This occurred in conjunction with a loss of responsiveness to other odorants. The instinctive behavioral response to the odor of ethanol was also enhanced. Importantly, there was a significant contributory link between the altered response to the odor of ethanol and increased ethanol avidity when assessed in the same animals. Here, we tested whether the neural and behavioral olfactory plasticity, and their relationship to enhanced ethanol intake, is a result of the mere exposure to ethanol or whether it requires the animal to associate ethanol's reinforcing properties with its odor attributes. In this later respect, the opioid system is important in the mediation (or modulation) of the reinforcing aspects of ethanol. To block endogenous opiates during prenatal life, pregnant rats received daily intraperitoneal administration of the opiate antagonist naltrexone from gestational day 6-21 jointly with ethanol delivered via diet. Relative to control progeny, we found that gestational exposure to naltrexone ameliorated the enhanced postnatal behavioral response to the odor of ethanol and postnatal drug avidity. Our findings support the proposition that in utero ethanol-induced olfactory plasticity (and its relationship to postnatal intake) requires, at least in part, the associative pairing between ethanol's odor quality and its reinforcing aspects. We also found suggestive evidence that fetal naltrexone ameliorated the untoward effects of gestational ethanol exposure on the neural response to non-fetal-exposure odorants. Thus, gestational naltrexone may also have a neuroprotective and/or neuroproliferative impact on olfactory development.

摘要

酒精暴露与青少年酗酒之间的关联已得到充分证实。最近的动物研究支持胎儿酒精暴露引起的化学感觉可塑性在这一观察结果中的作用。之前,我们已经证实,通过母体饮食在整个妊娠期给予胎儿酒精暴露会调节早期新生大鼠外周嗅觉系统对乙醇气味的神经反应。这与对其他气味的反应性丧失同时发生。对乙醇气味的本能行为反应也增强了。重要的是,在同一动物中评估时,对乙醇气味的反应改变与乙醇摄取量增加之间存在显著的关联。在这里,我们测试了神经和行为嗅觉可塑性,以及它们与增强的乙醇摄入量之间的关系,是仅仅由于暴露于乙醇还是需要动物将乙醇的强化特性与其气味属性相关联所致。在后一种情况下,阿片系统在介导(或调节)乙醇的强化方面很重要。为了在产前生活中阻断内源性阿片类药物,怀孕的老鼠从妊娠第 6-21 天每天接受腹膜内注射阿片拮抗剂纳曲酮,并通过饮食给予乙醇。与对照后代相比,我们发现妊娠暴露于纳曲酮可改善对新生后乙醇气味的增强行为反应和新生后药物摄取。我们的研究结果支持以下观点,即宫内乙醇引起的嗅觉可塑性(及其与产后摄入量的关系)至少部分需要乙醇气味质量与其强化方面之间的联想配对。我们还发现了一些暗示性的证据,表明胎儿纳曲酮可减轻妊娠乙醇暴露对非胎儿暴露气味的神经反应的不良影响。因此,妊娠纳曲酮可能对嗅觉发育具有神经保护和/或神经增殖作用。

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