Department of Molecular and Integrative Neurosciences, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Neuroscience. 2011 Dec 29;199:333-45. doi: 10.1016/j.neuroscience.2011.10.011. Epub 2011 Oct 18.
Substance abuse typically begins in adolescence; therefore, the impact of alcohol during this critical time in brain development is of particular importance. Epidemiological data indicate that excessive alcohol consumption is prevalent among adolescents and may have lasting neurobehavioral consequences. Loss of cholinergic input to the forebrain has been demonstrated following fetal alcohol exposure and in adults with Wernicke-Korsakoff syndrome. In the present study, immunohistochemistry for choline acetyltransferase (ChAT) was determined to assess forebrain cholinergic neurons (Ch1-4), and behavioral changes following periadolescent alcohol exposure. Wistar rats were exposed to intermittent ethanol vapor (14 h on/10 h off/day) for 35 days from postnatal day (PD) 22 to PD 57 (average blood alcohol concentration (BAC): 163 mg%). Rats were withdrawn from vapor and assessed for locomotor activity, startle response, conflict behavior in the open field, and immobility in the forced swim test, as adults. Rats were then sacrificed at day 71/72 and perfused for histochemical analyses. Ethanol vapor-exposed rats displayed: increased locomotor activity 8 h after the termination of vapor delivery for that 24 h period at day 10 and day 20 of alcohol vapor exposure, significant reductions in the amplitude of their responses to prepulse stimuli during the startle paradigm at 24 h withdrawal, and at 2 weeks following withdrawal, less anxiety-like and/or more "disinhibitory" behavior in the open field conflict, and more immobility in the forced swim test. Quantitative analyses of ChAT immunoreactivity revealed a significant reduction in cell counts in the Ch1-2 and Ch3-4 regions of the basal forebrain in ethanol vapor-exposed rats. This reduction in cell counts was significantly correlated with less anxiety-like and/or more "disinhibitory" behavior in the open field conflict test. These studies demonstrate that behavioral measures of arousal, affective state, disinhibitory behavior, and ChAT+IR, are all significantly impacted by periadolescent ethanol exposure and withdrawal in Wistar rats.
物质滥用通常始于青少年时期;因此,酒精在大脑发育的这个关键时期的影响尤为重要。流行病学数据表明,青少年过度饮酒较为普遍,可能会产生持久的神经行为后果。胎儿酒精暴露和韦尼克-科尔萨科夫综合征患者的前脑胆碱能输入已经减少。在本研究中,通过胆碱乙酰转移酶(ChAT)免疫组织化学来评估前脑胆碱能神经元(Ch1-4),并评估青春期后酒精暴露后的行为变化。Wistar 大鼠从出生后第 22 天(PD)到第 57 天(PD)接受间歇性乙醇蒸气暴露(每天 14 小时暴露/10 小时休息)(平均血酒精浓度(BAC):163mg%)。大鼠从蒸气中撤出,并在成年后评估其运动活动、惊跳反应、旷场中的冲突行为以及强迫游泳试验中的不动性。然后,大鼠在第 71/72 天被处死并进行组织化学分析。乙醇蒸气暴露的大鼠表现出:在第 10 天和第 20 天酒精蒸气暴露的 24 小时期间,在蒸气输送结束后 8 小时增加运动活动,在惊跳范式中对预脉冲刺激的反应幅度在 24 小时撤出时显著降低,并且在撤出后 2 周时,在旷场冲突中焦虑样和/或更多“去抑制”行为减少,在强迫游泳试验中不动性增加。ChAT 免疫反应的定量分析显示,乙醇蒸气暴露的大鼠基底前脑的 Ch1-2 和 Ch3-4 区域的细胞计数显著减少。这种细胞计数的减少与旷场冲突测试中焦虑样和/或更多“去抑制”行为的减少呈显著相关。这些研究表明,觉醒、情绪状态、去抑制行为和 ChAT+IR 的行为测量在 Wistar 大鼠青春期后乙醇暴露和撤出时均受到显著影响。