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可卡因:对其影响大鼠进食及相关行为的微观结构分析

Cocaine: a microstructural analysis of its effects on feeding and associated behaviour in the rat.

作者信息

Cooper S J, van der Hoek G A

机构信息

School of Psychology, University of Birmingham, UK.

出版信息

Brain Res. 1993 Apr 9;608(1):45-51. doi: 10.1016/0006-8993(93)90772-f.

Abstract

Cocaine (5.6-30 mg/kg, i.p.) was administered to nondeprived male rats trained to eat a palatable sweetened mash. Over a 60-min period, their behaviour was observed and recorded for a microstructural analysis. Cocaine suppressed feeding in a dose-dependent manner (significantly at 10 mg/kg and greater), and this was due in the main to a reduction in the frequency of eating bouts. In contrast, the mean duration of eating bouts was unaffected, except at the highest dose, 30 mg/kg. In addition, the rate of eating was not significantly affected by cocaine at any dose. Time-course data revealed that cocaine, at anorectic doses (10-30 mg/kg), initially suppressed feeding completely, and the duration of this suppression was proportional to the dose. In effect, cocaine delayed the initiation of feeding, thus bringing about the reduction in the number of eating bouts. Cocaine caused some stimulation of locomotor activity and rearing to the side of the observation tank, but did not affect rearing away from the centre, or immobility. Grooming proved to be very sensitive to cocaine's suppressant effect, with substantial inhibition occurring at 5.6 mg/kg (a sub-anorectic dose). These data are compared with previously published work with D-amphetamine and are contrasted with results for selective D1 and D2 dopamine receptor agonists.

摘要

将可卡因(5.6 - 30毫克/千克,腹腔注射)给予经过训练会食用美味甜味糊状物的非禁食雄性大鼠。在60分钟的时间段内,观察并记录它们的行为以进行微观结构分析。可卡因以剂量依赖的方式抑制进食(10毫克/千克及以上剂量时具有显著抑制作用),这主要是由于进食发作频率的降低。相比之下,进食发作的平均持续时间不受影响,除了最高剂量30毫克/千克时。此外,任何剂量的可卡因对进食速率均无显著影响。时间进程数据显示,厌食剂量(10 - 30毫克/千克)的可卡因最初会完全抑制进食,且这种抑制的持续时间与剂量成正比。实际上,可卡因延迟了进食的开始,从而导致进食发作次数减少。可卡因会对运动活动产生一定刺激,并使大鼠向观察箱一侧站立,但不影响大鼠远离中心站立或静止不动。事实证明,梳理毛发行为对可卡因的抑制作用非常敏感,在5.6毫克/千克(低于厌食剂量)时就会出现显著抑制。这些数据与先前发表的关于D - 苯丙胺的研究结果进行了比较,并与选择性D1和D2多巴胺受体激动剂的结果形成了对比。

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