Zhang Zhongqi, Morse Andrew C, Koob George F, Schulteis Gery
Department of Anesthesiology, UC San Diego School of Medicine and VA San Diego Healthcare System, San Diego, California 92161-5008, USA.
Alcohol Clin Exp Res. 2007 Nov;31(11):1811-9. doi: 10.1111/j.1530-0277.2007.00483.x. Epub 2007 Sep 14.
Withdrawal from acute bolus intraperitoneal (IP) injection of high doses of ethanol elicits anxiety-like behavior (e.g. Doremus et al., 2003; Gauvin et al., 1989, 1992) and conditioned place aversion (Morse et al., 2000). More recently we demonstrated that withdrawal from a single moderate dose of ethanol (2.0 g/kg) is accompanied by elevations in brain reward thresholds, and that repeated intermittent treatment with this dose results in a significant potentiation of reward deficit (Schulteis and Liu, 2006).
In the current study, the time- and dose-dependent emergence of anxiety-like behavior was measured in the elevated plus-maze at various times (3 to 24 hours) after acute or 3 daily IP injections of ethanol (1.0, 2.0, or 3.0 g/kg). Rats receiving daily handling for 2 days, and a single anxiety opportunity to explore the maze on a third day were divided into 1 of several treatment protocols: (1) NAIVE conditions: vehicle IP on all 3 days; (2) ACUTE conditions: vehicle on the first 2 days, ethanol on the third day; or (3) REPEAT conditions: ethanol on all 3 days.
ACUTE ethanol elicited reduced exploration of the open arms of the elevated plus-maze in a dose- and time-dependent fashion: 1.0 g/kg failed to elicit any significant effects, whereas 2.0 and 3.0 g/kg ethanol elicited a significant anxiety-like response at 6 hours and 9 to 12 hours postinjection, respectively. REPEAT treatment was still without effect at any time point tested following 1.0 g/kg ethanol, but extended the time course of anxiety-like behavior after treatment with either 2.0 or 3.0 g/kg doses. REPEAT treatment with 2.0 and 3.0 g/kg ethanol also produced significant hypoactivity in the maze at some time points postinjection.
Withdrawal from a single exposure to ethanol produces transient but significant anxiety-like behavior, and repeated intermittent bouts of intoxication result in a significant extension of the duration of effect. The rapid emergence and progression of negative emotional signs of withdrawal may be a significant factor in determining susceptibility to transition from casual drinking to loss of control and escalating patterns of consumption that result in alcoholism.
急性大剂量腹腔注射乙醇后戒断会引发焦虑样行为(如多雷穆斯等人,2003年;高文等人,1989年、1992年)和条件性位置厌恶(莫尔斯等人,2000年)。最近我们证明,单次中等剂量乙醇(2.0克/千克)戒断会伴随着脑奖赏阈值升高,且用此剂量反复间歇性治疗会导致奖赏缺陷显著增强(舒尔泰斯和刘,2006年)。
在本研究中,在急性或连续3天腹腔注射乙醇(1.0、2.0或3.0克/千克)后的不同时间(3至24小时),于高架十字迷宫中测量焦虑样行为出现的时间和剂量依赖性。接受2天每日处理且在第3天有一次探索迷宫的焦虑机会的大鼠被分为几种处理方案之一:(1)空白对照条件:3天均腹腔注射赋形剂;(2)急性条件:前2天注射赋形剂,第3天注射乙醇;或(3)重复条件:3天均注射乙醇。
急性乙醇以剂量和时间依赖性方式减少了对高架十字迷宫开放臂的探索:1.0克/千克未引发任何显著影响,而2.0和3.0克/千克乙醇分别在注射后6小时和9至12小时引发了显著的焦虑样反应。1.0克/千克乙醇重复治疗在任何测试时间点均无效果,但在用2.0或3.0克/千克剂量治疗后延长了焦虑样行为的时间进程。2.0和3.0克/千克乙醇重复治疗在注射后某些时间点也在迷宫中产生了显著的活动减少。
单次接触乙醇后戒断会产生短暂但显著的焦虑样行为,反复间歇性中毒发作会导致效应持续时间显著延长。戒断负面情绪迹象的快速出现和进展可能是决定从偶尔饮酒转变为失控和饮酒量不断增加模式(导致酗酒)易感性的一个重要因素。