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阿片类激动剂和拮抗剂对大鼠液体摄入及糖精选择的影响。

Effects of opiate agonists and antagonists on fluid intake and saccharin choice in the rat.

作者信息

Cooper S J

出版信息

Neuropharmacology. 1983 Mar;22(3):323-8. doi: 10.1016/0028-3908(83)90247-2.

Abstract

Both naloxone (3 and 10 mg X kg-1) and naltrexone (1-10 mg X kg-1) abolished the preference for a highly palatable 0.05% sodium saccharin solution in rats that had been adapted to a 22 hr water-deprivation schedule. The effect occurred as a result of a selective decrease in the consumption of the saccharin solution, since the intake of water, which was concurrently available in the two-fluid choice test, remained unaffected. When a less preferred saccharin solution was used (0.01%), naltrexone exerted a similar suppressant effect on the sodium preference, whilst naloxone failed to produce significant effects on the intake of saccharin solution or water. The data for the opiate agonists were interpreted in terms of a drug-induced blockade of the natural reward of highly palatable fluids in thirsty rats. In the same choice test, morphine and a stabilised enkephalin analogue, with a selective agonist action at mu-opiate receptors (RX783030), failed to influence the preference for the palatable saccharin solutions. In water-deprived animals, at least, exogenous opiate agonists, active at mu-receptors, did not appear to influence the reward of the palatable solutions.

摘要

纳洛酮(3和10毫克/千克)和纳曲酮(1 - 10毫克/千克)均消除了已适应22小时禁水方案的大鼠对高适口性0.05%糖精钠溶液的偏好。这种效应是由于糖精溶液的消耗量选择性降低所致,因为在双液选择试验中同时提供的水的摄入量未受影响。当使用较不受欢迎的糖精溶液(0.01%)时,纳曲酮对钠偏好产生了类似的抑制作用,而纳洛酮对糖精溶液或水的摄入量未产生显著影响。阿片类激动剂的数据被解释为药物诱导对口渴大鼠中高适口性液体的天然奖赏的阻断。在相同的选择试验中,吗啡和一种稳定的脑啡肽类似物,对μ - 阿片受体具有选择性激动作用(RX783030),未能影响对适口性糖精溶液的偏好。至少在缺水动物中,作用于μ - 受体的外源性阿片类激动剂似乎并未影响适口性溶液的奖赏。

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