Getachew Bruk, Hauser Sheketha R, Taylor Robert E, Tizabi Yousef
Department of Pharmacology, College of Medicine, Howard University, 520 W Street NW, Washington, DC 20059, USA.
Pharmacol Biochem Behav. 2008 Nov;91(1):97-103. doi: 10.1016/j.pbb.2008.06.016. Epub 2008 Jun 29.
Epidemiological studies indicate significant co-morbid expression of alcoholism, anxiety, and depression. These symptoms are often under-diagnosed and under-treated and can worsen prognostic and treatment outcome for alcoholism. Nonetheless, a causal relationship between alcoholism and these conditions is yet to be established. In this study we sought to determine the effects of daily alcohol administration on the indices of anxiety and depression in two rat strains, one of which exhibits inherent depressive-like characteristics. Moreover, it was of relevance to examine the effects of a clinically useful antidepressant on alcohol-induced behavioral changes. Wistar-Kyoto (WKY) rats derived from Wistar stock show low levels of locomotor activity in an open field and high levels of immobility in the forced swim test (FST) which is considered a measure of their helplessness and hence are considered a putative animal model of depression. Adult female WKY and Wistar rats were exposed for 3 hrs daily to 95% ethanol vapor to achieve a mean blood alcohol level (BAL) of approximately 150 mg/dL. Controls were exposed to air in similar inhalation chambers. Sixteen to 18 hrs following 7 or 14 days of exposure to alcohol, locomotor activity (LCA) in open field, duration of time spent in the open arm of the elevated plus-maze (EPM), reflective of anxiety-like behavior and immobility in FST were evaluated. Alcohol exposure for 7 or 14 days reduced LCA only in Wistar rats but enhanced FST immobility in both strains at both time points. Only 14 day alcohol exposure reduced EPM open arm time in both WKY and Wistar rats. Daily treatment with desipramine (8 mg/kg) blocked all the changes induced by alcohol in both strains. Thus, subchronic (7 day) exposure to alcohol induces depressive-like characteristics in Wistar rats and exacerbates that of WKY rats. Chronic (14 day) exposure, however, also induces an anxiety-like effect in both strains. The depressive- and anxiety-like behaviors induced by alcohol were blocked by daily treatment with a tricyclic antidepressant. It may be suggested that prophylactic treatment of alcoholics with an antidepressant prior to detoxification may improve treatment outcome for alcoholism.
流行病学研究表明,酒精中毒、焦虑和抑郁存在显著的共病表现。这些症状常常诊断不足且治疗不充分,会使酒精中毒的预后和治疗效果恶化。尽管如此,酒精中毒与这些病症之间的因果关系尚未确立。在本研究中,我们试图确定每日给予酒精对两种大鼠品系焦虑和抑郁指标的影响,其中一种品系表现出固有的类抑郁特征。此外,研究临床上有用的抗抑郁药对酒精诱导的行为变化的影响也具有相关性。源自Wistar种群的Wistar-Kyoto(WKY)大鼠在旷场试验中表现出低水平的自发活动,在强迫游泳试验(FST)中表现出高水平的不动时间,该试验被认为是衡量其无助感的指标,因此被视为一种假定的抑郁动物模型。成年雌性WKY和Wistar大鼠每天暴露于95%乙醇蒸气中3小时,以达到平均血液酒精水平(BAL)约150mg/dL。对照组在类似的吸入舱中暴露于空气中。在暴露于酒精7天或14天后的16至18小时,评估旷场试验中的自发活动(LCA)、高架十字迷宫(EPM)开放臂中停留的时间(反映类焦虑行为)以及FST中的不动时间。暴露于酒精7天或14天仅降低了Wistar大鼠的LCA,但在两个时间点均增加了两种品系的FST不动时间。仅14天的酒精暴露减少了WKY和Wistar大鼠的EPM开放臂时间。每日用去甲丙咪嗪(8mg/kg)治疗可阻断两种品系中酒精诱导的所有变化。因此,亚慢性(7天)暴露于酒精会在Wistar大鼠中诱导类抑郁特征,并加剧WKY大鼠的类抑郁特征。然而,慢性(14天)暴露也会在两种品系中诱导类焦虑效应。酒精诱导的类抑郁和类焦虑行为可通过每日用三环类抗抑郁药治疗来阻断。可以推测,在戒酒前用抗抑郁药对酒精中毒者进行预防性治疗可能会改善酒精中毒的治疗效果。