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母体给予维生素C和E对豚鼠乙醇神经行为致畸性的影响。

Effects of maternal administration of vitamins C and E on ethanol neurobehavioral teratogenicity in the guinea pig.

作者信息

Nash Christopher M, Ibram Ferda, Dringenberg Hans C, Reynolds James N, Brien James F

机构信息

Department of Pharmacology & Toxicology, Queen's University, Kingston, Ontario K7L 3N6, Canada.

出版信息

Alcohol. 2007 Dec;41(8):577-86. doi: 10.1016/j.alcohol.2007.08.005. Epub 2007 Nov 5.

Abstract

Consumption of ethanol during human pregnancy can produce a wide spectrum of teratogenic effects, including neurobehavioral dysfunction. This study, in the guinea pig, tested the hypothesis that chronic maternal administration of antioxidant vitamins C plus E, together with ethanol, mitigates ethanol neurobehavioral teratogenicity. Pregnant guinea pigs received one of the following four chronic oral regimens: ethanol and vitamins C plus E; ethanol and vitamin vehicle; isocaloric-sucrose/pair-feeding and vitamins C plus E; or isocaloric-sucrose/pair-feeding and vehicle. Vitamins C (250 mg) plus E (100mg) or vehicle were given daily, and ethanol (4 g/kg maternal body weight/day) (E) or isocaloric-sucrose/pair-feeding was given for 5 consecutive days followed by 2 days of no treatment each week throughout gestation. One neonate from selected litters was studied on postnatal day (PD) 0. Neurobehavioral function was determined by measuring task acquisition and task retention using an 8-day moving-platform version of the Morris water-maze task, starting on PD 45. Thereafter, in vivo electrophysiologic assessment of changes in hippocampal synaptic plasticity was conducted. There was an ethanol-induced decrease in neonatal brain weight compared with sucrose. The vitamins C plus E regimen protected hippocampal weight relative to brain weight in ethanol offspring, and mitigated the ethanol-induced deficit in the task-retention component of the water-maze task. However, in the sucrose group, this Vit regimen produced deficits in both task acquisition and task retention. The vitamins C plus E regimen did not mitigate the ethanol-induced impairment of hippocampal long-term potentiation. These results indicate that maternal administration of this high-dose vitamins C plus E regimen throughout gestation has limited efficacy and potential adverse effects as a therapeutic intervention for E neurobehavioral teratogenicity.

摘要

人类孕期摄入乙醇会产生一系列致畸作用,包括神经行为功能障碍。本研究以豚鼠为对象,检验了以下假设:孕期母体长期给予抗氧化维生素C和E以及乙醇,可减轻乙醇的神经行为致畸性。怀孕的豚鼠接受以下四种长期口服方案之一:乙醇与维生素C加E;乙醇与维生素赋形剂;等热量蔗糖/配对喂养与维生素C加E;或等热量蔗糖/配对喂养与赋形剂。每天给予维生素C(250毫克)加E(100毫克)或赋形剂,乙醇(4克/千克母体体重/天)(E)或等热量蔗糖/配对喂养持续5天,然后在整个妊娠期每周有2天不进行处理。从选定的窝中选取一只新生幼崽在出生后第0天进行研究。从出生后第45天开始,使用8天移动平台版的莫里斯水迷宫任务,通过测量任务习得和任务保持来确定神经行为功能。此后,对海马突触可塑性变化进行体内电生理评估。与蔗糖组相比,乙醇导致新生幼崽脑重量下降。维生素C加E方案相对于乙醇组后代的脑重量保护了海马体重量,并减轻了乙醇诱导的水迷宫任务中任务保持部分的缺陷。然而,在蔗糖组中,这种维生素方案在任务习得和任务保持方面均产生了缺陷。维生素C加E方案并未减轻乙醇诱导的海马体长期增强损伤。这些结果表明,孕期母体全程给予这种高剂量维生素C加E方案作为乙醇神经行为致畸性的治疗干预措施,疗效有限且存在潜在不良反应。

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