Department of Psychology, Center for Behavioral Teratology, San Diego State University, San Diego, California, USA.
Hippocampus. 2012 Mar;22(3):619-30. doi: 10.1002/hipo.20925. Epub 2011 May 3.
Children exposed to alcohol prenatally suffer from a range of physical, neuropathological, and behavioral alterations, referred to as fetal alcohol spectrum disorders (FASD). Both the cerebellum and hippocampus are affected by alcohol exposure during development, which may contribute to behavioral and cognitive deficits observed in children with FASD. Despite the known neuropathology associated with prenatal alcohol exposure, many pregnant women continue to drink (heavy drinkers, in particular), creating a need to identify effective treatments for their children who are adversely affected by alcohol. We previously reported that choline supplementation can mitigate alcohol's effects on cognitive development, specifically on tasks which depend on the functional integrity of the hippocampus. The present study examined whether choline supplementation could differentially mitigate alcohol's effects on trace eyeblink classical conditioning (ECC, a hippocampal-dependent task) and delay ECC (a cerebellar-dependent task). Long-Evans rats were exposed to 5.25 g/kg/day alcohol via gastric intubation from postnatal days (PD) 4-9, a period of brain development equivalent to late gestation in humans. A sham-intubated control group was included. From PD 10-30, subjects received subcutaneous injections of 100 mg/kg choline chloride or vehicle. Beginning on PD 32-34, subjects were trained on either delay or trace eyeblink conditioning. Performance of subjects exposed to alcohol was significantly impaired on both tasks, as indicated by significant reductions in percentage and amplitude of conditioned eyeblink responses, an effect that was attenuated by choline supplementation on the trace, but not delay conditioning task. Indeed, alcohol-exposed subjects treated with choline performed at control levels on the trace eyeblink conditioning task. There were no significant main or interactive effects of sex. These data indicate that choline supplementation can significantly reduce the severity of trace eyeblink conditioning deficits associated with early alcohol exposure, even when administered after the alcohol insult is complete. These findings have important implications for the treatment of fetal alcohol spectrum disorders.
产前暴露于酒精的儿童会出现一系列身体、神经病理学和行为改变,被称为胎儿酒精谱系障碍(FASD)。小脑和海马体在发育过程中都会受到酒精暴露的影响,这可能导致 FASD 儿童出现行为和认知缺陷。尽管已知与产前酒精暴露相关的神经病理学,但许多孕妇仍继续饮酒(尤其是重度饮酒者),这就需要为其受酒精影响的孩子寻找有效的治疗方法。我们之前曾报道过,胆碱补充可以减轻酒精对认知发育的影响,特别是对依赖海马体功能完整性的任务。本研究旨在探讨胆碱补充是否可以减轻酒精对痕迹性眨眼条件反射(ECC,一种依赖于海马体的任务)和延迟性 ECC(一种依赖于小脑的任务)的影响。Long-Evans 大鼠在出生后第 4-9 天(相当于人类妊娠晚期)通过胃管每天接受 5.25 克/千克的酒精灌胃。包括假灌胃对照组。从第 10-30 天,实验组接受 100mg/kg 氯化胆碱或载体的皮下注射。从第 32-34 天开始,对动物进行延迟或痕迹性眨眼条件反射训练。暴露于酒精的动物在两个任务中的表现均显著受损,表现为条件性眨眼反应的百分比和幅度显著降低,胆碱补充可减轻痕迹性但不能减轻延迟性条件反射任务的影响。事实上,接受胆碱补充的酒精暴露动物在痕迹性眨眼条件反射任务中的表现达到了对照组的水平。性别没有显著的主效应或交互作用。这些数据表明,即使在酒精暴露后给予胆碱补充,也可以显著减轻与早期酒精暴露相关的痕迹性眨眼条件反射缺陷的严重程度。这些发现对胎儿酒精谱系障碍的治疗具有重要意义。