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阿立哌唑对大鼠精神兴奋剂戒断后自然奖赏操作性反应的影响。

Effects of aripiprazole on operant responding for a natural reward after psychostimulant withdrawal in rats.

作者信息

Schwabe Kerstin, Koch Michael

机构信息

Department of Neurosurgery, Medical University, MHH, Carl-Neuberg-Str. 1, 30625, Hanover, Germany.

出版信息

Psychopharmacology (Berl). 2007 Apr;191(3):759-65. doi: 10.1007/s00213-006-0520-2. Epub 2006 Sep 5.

Abstract

RATIONALE

Withdrawal from repeated amphetamine administration has been shown to decrease the motivation to work for a natural reward in rats, a phenomenon thought to be associated with hypofunction of the mesolimbic dopamine system.

OBJECTIVES

We tested whether aripiprazole, a partial dopamine receptor agonist, can restore the animals' responding for reward pellets after amphetamine withdrawal.

MATERIALS AND METHODS

Rats were trained to lever-press for food pellets under a progressive ratio-schedule of reinforcement. After reaching a stable breakpoint, i.e., the highest ratio completed, one group was injected ten times with increasing doses of amphetamine (1 to 10 mg/kg, three times a day for 4 days), while the other group received vehicle injections. The rats were again tested for their breakpoint 24 h after the last amphetamine injection under 0.0, 0.25, 0.75, and 2.5 mg/kg aripiprazole.

RESULTS

Withdrawal from repeated amphetamine injection reduced the breakpoint while low doses of aripiprazole (0.25 and 0.75 mg/kg) prevented this effect. In addition, the rats needed a longer time for the first 20 pellets (fixed ratio-schedule training before starting the progressive ratio-schedule) after amphetamine withdrawal but not after subsequent injection with aripiprazole. It is notable that the injection of 2.5 mg/kg aripiprazole reduced responding for reward pellets and prolonged the duration for the first 20 pellets irrespective of previous amphetamine or vehicle treatment. However, withdrawal from repeated administration of 0.25 and 2.5 mg/kg aripiprazole did not reduce responding for reward pellets.

CONCLUSIONS

These results suggest that aripiprazole may have potential use as a treatment for the motivational effects of the acute withdrawal stage of the psychostimulant addiction cycle.

摘要

理论依据

研究表明,反复给予大鼠苯丙胺后停药,会降低其为获取自然奖励而工作的动机,这种现象被认为与中脑边缘多巴胺系统功能减退有关。

目的

我们测试了阿立哌唑(一种部分多巴胺受体激动剂)能否在苯丙胺停药后恢复动物对奖励颗粒的反应。

材料与方法

在渐进性比率强化程序下,训练大鼠按压杠杆以获取食物颗粒。达到稳定的断点(即完成的最高比率)后,一组大鼠接受十次递增剂量的苯丙胺注射(1至10毫克/千克,每天三次,共4天),另一组接受溶剂注射。在最后一次苯丙胺注射24小时后,在0.0、0.25、0.75和2.5毫克/千克阿立哌唑的条件下,再次测试大鼠的断点。

结果

反复注射苯丙胺后停药会降低断点,而低剂量的阿立哌唑(0.25和0.75毫克/千克)可防止这种效应。此外,苯丙胺停药后,大鼠获取前20颗颗粒所需时间更长(在开始渐进性比率程序训练前进行固定比率程序训练),但在随后注射阿立哌唑后则不然。值得注意的是,无论先前接受苯丙胺还是溶剂治疗,注射2.5毫克/千克阿立哌唑都会降低对奖励颗粒的反应,并延长获取前20颗颗粒的时间。然而,反复给予0.25和2.5毫克/千克阿立哌唑后停药,并未降低对奖励颗粒的反应。

结论

这些结果表明,阿立哌唑可能具有治疗精神兴奋剂成瘾周期急性戒断阶段动机效应的潜在用途。

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