Hilakivi L, Sinclair J D
Pharmacol Biochem Behav. 1986 May;24(5):1451-5. doi: 10.1016/0091-3057(86)90209-1.
In order to test further the hypothesis that neonatal active (REM) sleep suppression by means of clomipramine, an inhibitor of monoamine reuptake, is involved in the subsequent increase of voluntary alcohol consumption in rats, the AA (alcohol preferring) and ANA (alcohol avoiding) rat lines were injected daily with 25 mg/kg clomipramine IP from the 7th to the 20th postnatal days. At the age of 3 months the clomipramine AA rats consumed significantly more 10% (v/v) alcohol solution than the control AA rats. Neonatal clomipramine treatment did not, however, affect the drinking patterns of the ANA rats. Secondly, in order to test the alcohol-deprivation effect; i.e., the increase in alcohol consumption after its deprivation, the AA and ANA rats were deprived of alcohol for 17 days. There was a significant difference between the temporal pattern of changes in alcohol drinking produced by alcohol deprivation in the AA rats and the pattern in the ANA rats. Furthermore, the clomipramine treated AA rats tended to show a decrease and the clomipramine ANA rats an increase in their post-deprivation alcohol intake compared to the control AA and ANA rats. The results are interpreted in terms of active sleep being important for later alcohol drinking and other genetically determined differences in behavior.
通过单胺再摄取抑制剂氯米帕明抑制新生大鼠的主动(快速眼动)睡眠,与随后大鼠自愿饮酒量增加有关,从出生后第7天至第20天,每天给酒精偏好(AA)和酒精回避(ANA)大鼠品系腹腔注射25 mg/kg氯米帕明。3个月大时,氯米帕明处理的AA大鼠比对照AA大鼠消耗的10%(v/v)酒精溶液显著更多。然而,新生期氯米帕明处理并未影响ANA大鼠的饮酒模式。其次,为了测试酒精剥夺效应,即酒精剥夺后饮酒量的增加,对AA和ANA大鼠进行17天的酒精剥夺。AA大鼠和ANA大鼠因酒精剥夺导致的饮酒量变化的时间模式存在显著差异。此外,与对照AA和ANA大鼠相比,氯米帕明处理的AA大鼠剥夺后酒精摄入量倾向于减少,而氯米帕明处理的ANA大鼠则增加。这些结果被解释为主动睡眠对后期饮酒很重要,以及行为中其他由基因决定的差异。