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大鼠经口自行摄取皮质酮。

Rats orally self-administer corticosterone.

作者信息

Deroche V, Piazza P V, Deminière J M, Le Moal M, Simon H

机构信息

Laboratoire de Psychobiologie des Comportements Adaptatifs, INSERM U259, Université de Bordeaux II, France.

出版信息

Brain Res. 1993 Sep 17;622(1-2):315-20. doi: 10.1016/0006-8993(93)90837-d.

DOI:10.1016/0006-8993(93)90837-d
PMID:8242374
Abstract

Corticosterone, the major glucocorticoid in the rat, may modulate the reinforcing properties of addictive drugs as well as act as a positive reinforcer for intravenous self-administration. Since glucocorticoids are generally administered to humans via the oral route, we examined the ability of corticosterone to induce oral self-administration in the rat. In a first experiment, animals with free access to food could choose between a corticosterone solution and water. Three doses (25, 50 and 100 micrograms/ml) were tested. The group receiving the 100 micrograms/ml dose was also submitted to an extinction followed by a reversal test. In a second experiment, we examined whether the reinforcing properties of corticosterone could induce drinking independently of food intake. In the pre-test phase rats had access to food only during a fixed period of the day (11.00 h to 14.00 h). Corticosterone solution (200 micrograms/ml) or tap water were available during this period, with free access to tap water for the rest of the day. During the test period, access to food was shifted forward in time, while the availability of the corticosterone solution remained the same. The first experiment showed that rats preferred a corticosterone solution to tap water, developing self-administration in a dose-dependent manner. This preference could be extinguished, but was regained during the reversal phase. In the second experiment, animals that had access to the corticosterone solution drank more than rats that had access to water in the absence of food. These results indicate that corticosterone has reinforcing properties after oral administration.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

皮质酮是大鼠体内主要的糖皮质激素,它可能会调节成瘾性药物的强化特性,并作为静脉自我给药的阳性强化物。由于糖皮质激素通常通过口服途径给予人类,我们研究了皮质酮诱导大鼠口服自我给药的能力。在第一个实验中,可自由获取食物的动物可以在皮质酮溶液和水之间进行选择。测试了三种剂量(25、50和100微克/毫升)。接受100微克/毫升剂量的组也进行了消退实验,随后进行了反转测试。在第二个实验中,我们研究了皮质酮的强化特性是否能在不依赖食物摄入的情况下诱导饮水。在预测试阶段,大鼠仅在一天中的固定时间段(11:00至14:00)可以获取食物。在此期间提供皮质酮溶液(200微克/毫升)或自来水,其余时间可自由饮用自来水。在测试期间,获取食物的时间提前,而皮质酮溶液的供应保持不变。第一个实验表明,大鼠更喜欢皮质酮溶液而不是自来水,并以剂量依赖的方式形成自我给药行为。这种偏好可以被消除,但在反转阶段又会恢复。在第二个实验中,能够获取皮质酮溶液的动物比在没有食物时只能获取水的大鼠饮水量更多。这些结果表明,皮质酮口服后具有强化特性。(摘要截断于250字)

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