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阿片类药物戒断小鼠进食动机增加。

Increased motivation to eat in opiate-withdrawn mice.

机构信息

Addicteam, Université de Bordeaux, CNRS UMR 5287, 146 rue Léo Saignat, 33076, Bordeaux, France.

出版信息

Psychopharmacology (Berl). 2012 Jun;221(4):675-84. doi: 10.1007/s00213-011-2612-x. Epub 2011 Dec 30.

Abstract

RATIONALE

In drug-dependent individuals, the primary excessive motivation is for drugs. Studies also indicate altered interest for "natural" rewarding activities associated with motivational disorders that may be relevant to drug dependence. However, to date, the impact of drug dependence and withdrawal upon motivation for "natural" rewards remains unclear.

METHODS AND OBJECTIVES

In the present study, we use a food-driven operant behavior paradigm to assess the impact of opiate intake and withdrawal upon the motivational properties of highly palatable food (HPF) in mice.

RESULTS

Our findings indicate that early (8-h) opiate withdrawal does not affect either the motivational or the discriminative properties of HPF intake. However, starting 32 h after the last morphine injection, opiate withdrawal increases operant behavior aimed at obtaining HPF. The increased HPF-driven behavior lasts at least 12 days following opiate withdrawal, indicating long-lasting effects upon motivation. Using a paradigm of reward contingency reversal, we also address the impact of opiate withdrawal upon cognitive functions. Our results indicate that opiate withdrawal does not affect the ability to learn a new operant rule to obtain HPF. Indeed, opiate withdrawal ameliorates the acquisition of the new HPF-driven operant task, most probably due to the persistent and long-lasting increased motivation. Finally, analysis of ambulatory activity and body weight (BW) changes reveal that motivational and cognitive effects are totally independent of caloric and/or motor effects of opiate dosing and withdrawal.

CONCLUSIONS

These results clearly demonstrate that excessive opiate intake and withdrawal produces dramatic and long-lasting motivational disorders relevant to drug dependence.

摘要

理由

在药物依赖个体中,主要的过度动机是药物。研究还表明,与动机障碍相关的“自然”奖励活动的兴趣发生改变,这可能与药物依赖有关。然而,迄今为止,药物依赖和戒断对“自然”奖励动机的影响仍不清楚。

方法和目的

在本研究中,我们使用食物驱动的操作性行为范式来评估阿片类药物摄入和戒断对小鼠高可口食物(HPF)的动机特性的影响。

结果

我们的研究结果表明,早期(8 小时)阿片类药物戒断既不会影响 HPF 摄入的动机性也不会影响其辨别性。然而,从最后一次吗啡注射后 32 小时开始,阿片类药物戒断增加了获得 HPF 的操作性行为。这种增加的 HPF 驱动行为至少持续 12 天,表明对动机有持久的影响。通过奖励关联反转的范式,我们还解决了阿片类药物戒断对认知功能的影响。我们的结果表明,阿片类药物戒断不会影响获得 HPF 的新操作性规则的能力。实际上,阿片类药物戒断改善了新的 HPF 驱动操作性任务的获得,这很可能是由于持续且持久的动机增加。最后,对活动和体重(BW)变化的分析表明,动机和认知效应完全独立于阿片类药物剂量和戒断的热量和/或运动效应。

结论

这些结果清楚地表明,过量的阿片类药物摄入和戒断会导致与药物依赖相关的剧烈和持久的动机障碍。

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