Graduate School of Biomedical Sciences, University of Maine, Orono, Maine 04469-5742, USA.
Alcohol Clin Exp Res. 2012 Mar;36(3):467-76. doi: 10.1111/j.1530-0277.2011.01634.x. Epub 2011 Oct 20.
Alcohol withdrawal is associated with behavioral and chronobiological disturbances that may persist during protracted abstinence. We previously reported that C57BL/6J (B6) mice show marked but temporary reductions in running-wheel activity, and normal free-running circadian rhythms, following a 4-day chronic intermittent ethanol (CIE) vapor exposure (16 hours of ethanol vapor exposure alternating with 8 hours of withdrawal). In the present experiments, we extend these observations in 2 ways: (i) by examining post-CIE locomotor activity in C3H/HeJ (C3H) mice, an inbred strain characterized by high sensitivity to ethanol withdrawal, and (ii) by directly comparing the responses of B6 and C3H mice to a longer-duration CIE protocol.
In Experiment 1, C3H mice were exposed to the same 4-day CIE protocol used in our previous study with B6 mice (referred to here as the 1-cycle CIE protocol). In Experiment 2, C3H and B6 mice were exposed to 3 successive 4-day CIE cycles, each separated by 2 days of withdrawal (the 3-cycle CIE protocol). Running-wheel activity was monitored prior to and following CIE, and post-CIE activity was recorded in constant darkness to allow assessment of free-running circadian period and phase.
C3H mice displayed pronounced reductions in running-wheel activity that persisted for the duration of the recording period (up to 30 days) following both 1-cycle (Experiment 1) and 3-cycle (Experiment 2) CIE protocols. In contrast, B6 mice showed reductions in locomotor activity that persisted for about 1 week following the 3-cycle CIE protocol, similar to the results of our previous study using a 1-cycle protocol in this strain. Additionally, C3H mice showed significant shortening of free-running period following the 3-cycle, but not the 1-cycle, CIE protocol, while B6 mice showed normal free-running rhythms.
These results reveal genetic differences in the persistence of ethanol withdrawal-induced hypo-locomotion. In addition, chronobiological alterations during extended abstinence may depend on both genetic susceptibility and an extended prior withdrawal history. The present data establish a novel experimental model for long-term behavioral and circadian disruptions associated with ethanol withdrawal.
酒精戒断与行为和生物钟紊乱有关,这些紊乱在长期戒断期间可能持续存在。我们之前的研究报告称,C57BL/6J(B6)小鼠在经历了为期 4 天的慢性间歇性乙醇(CIE)蒸气暴露(16 小时的乙醇蒸气暴露与 8 小时的戒断交替)后,表现出明显但短暂的跑步轮活动减少,以及正常的自由运行昼夜节律。在本实验中,我们以两种方式扩展了这些观察结果:(i)通过检查对 C3H/HeJ(C3H)小鼠的 CIE 后运动活动,C3H 是一种对内源性乙醇戒断敏感的近交系;(ii)通过直接比较 B6 和 C3H 小鼠对较长时间 CIE 方案的反应。
在实验 1 中,C3H 小鼠接受了与我们之前使用 B6 小鼠的研究中相同的为期 4 天的 CIE 方案(此处称为 1 个周期的 CIE 方案)。在实验 2 中,C3H 和 B6 小鼠接受了 3 个连续的 4 天 CIE 周期,每个周期之间有 2 天的戒断(3 个周期的 CIE 方案)。在 CIE 之前和之后监测跑步轮活动,在持续黑暗中记录 CIE 后的活动,以评估自由运行昼夜周期和相位。
C3H 小鼠在 1 个周期(实验 1)和 3 个周期(实验 2)CIE 方案后,其跑步轮活动明显减少,持续记录期(长达 30 天)。相比之下,B6 小鼠在接受 3 个周期的 CIE 方案后,运动活动减少持续了大约 1 周,这与我们之前在该品系中使用 1 个周期方案的研究结果相似。此外,C3H 小鼠在接受 3 个周期的 CIE 方案后,自由运行周期明显缩短,但在接受 1 个周期的 CIE 方案后则没有变化,而 B6 小鼠则表现出正常的自由运行节律。
这些结果揭示了与乙醇戒断相关的运动减少持续时间的遗传差异。此外,在长时间戒断期间的生物钟改变可能取决于遗传易感性和延长的先前戒断史。本数据为与乙醇戒断相关的长期行为和昼夜节律紊乱建立了一个新的实验模型。