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三重单胺摄取抑制剂 DOV 102,677 对酒精偏爱(P)大鼠酒精动机反应和抗抑郁活性的影响。

Effects of the triple monoamine uptake inhibitor DOV 102,677 on alcohol-motivated responding and antidepressant activity in alcohol-preferring (P) rats.

机构信息

Department of Psychiatry and Behavioral Sciences, Howard University College of Medicine, Washington, DC, USA.

出版信息

Alcohol Clin Exp Res. 2012 May;36(5):863-73. doi: 10.1111/j.1530-0277.2011.01671.x. Epub 2011 Dec 7.

Abstract

BACKGROUND

Concurrent inhibitors of dopamine, norepinephrine, and serotonin uptake have been proposed as novel antidepressants. Given the high comorbidity between alcoholism and depression, we evaluated the activity of DOV 102,677 (DOV) on alcohol-maintained responding and performance in the forced swim test (FST), a model of antidepressant (AD) activity, using alcohol-preferring (P) rats.

METHODS

Following training to lever press for either alcohol (10% v/v) or sucrose (3, 2%, w/v) on a fixed-ratio 4 (FR4) schedule, DOV (1.56 to 50 mg/kg; PO) was given 25 minutes or 24 hours prior to evaluation. The effects of DOV (12.5 to 50 mg/kg; PO) in the FST were evaluated 25 minutes posttreatment.

RESULTS

DOV (6.25 to 50 mg/kg) dose-dependently reduced alcohol-maintained responding by 59 to 88% at 25 minutes posttreatment, without significantly altering sucrose responding. The reduction in alcohol responding (44% at 50 mg/kg) was sustained for up to 120 hours after a single dose. Administration of a single dose of DOV (25, 50 mg/kg) 24 hours before testing suppressed alcohol responding for 48 hours by 59 to 62%. DOV (12.5 to 50 mg/kg) also dose-dependently reduced immobility of P rats in the FST.

CONCLUSIONS

DOV produces both prolonged and selective reductions of alcohol-motivated behaviors in P rats. The elimination kinetics of DOV suggests that its long duration of action may be due to an active metabolite. DOV also produced robust AD-like effects in P rats. We propose that DOV may be useful in treating comorbid alcoholism and depression in humans.

摘要

背景

同时抑制多巴胺、去甲肾上腺素和 5-羟色胺摄取被认为是新型抗抑郁药。鉴于酒精中毒和抑郁症之间的高共病性,我们评估了 DOV 102,677(DOV)对酒精维持反应和强迫游泳试验(FST)中抗抑郁(AD)活性的影响,使用酒精偏好(P)大鼠。

方法

在训练大鼠通过按压杠杆来获得酒精(10%v/v)或蔗糖(3、2%w/v)后,通过固定比率 4(FR4)方案,给予 DOV(1.56 至 50mg/kg;PO),在评估前 25 分钟或 24 小时给予。在治疗后 25 分钟评估 DOV(12.5 至 50mg/kg;PO)在 FST 中的作用。

结果

DOV(6.25 至 50mg/kg)剂量依赖性地在治疗后 25 分钟减少了 59%至 88%的酒精维持反应,而对蔗糖反应没有显著影响。单次给药后,酒精反应减少(50mg/kg 时减少 44%)可持续长达 120 小时。单次给予 DOV(25、50mg/kg)24 小时前,可抑制 48 小时内的酒精反应,减少 59%至 62%。DOV(12.5 至 50mg/kg)也剂量依赖性地降低了 P 大鼠在 FST 中的不动性。

结论

DOV 可延长并选择性地减少 P 大鼠的酒精动机行为。DOV 的消除动力学表明,其长作用时间可能是由于其活性代谢物。DOV 还在 P 大鼠中产生了强大的 AD 样作用。我们提出 DOV 可能对治疗人类共病的酒精中毒和抑郁症有用。

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