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纳洛酮及吗啡耐受性对吗啡、哌替啶和去甲哌替啶行为效应的影响

Modification of behavioral effects of morphine, meperidine and normeperidine by naloxone and by morphine tolerance.

作者信息

Witkin J M, Leander J D, Dykstra L A

出版信息

J Pharmacol Exp Ther. 1983 May;225(2):275-83.

PMID:6842391
Abstract

Lever-press responding of morphine-tolerant and nontolerant squirrel monkeys was maintained under a multiple fixed-interval 5-min, fixed-interval 5-min schedule of food or electric shock presentation. Under the multiple schedule, the first response after a 5-min interval produced either food or shock depending on the prevailing stimulus. Responding maintained by either food or shock was characterized by patterns of positively accelerated responding during the 5-min interval. Morphine (0.1-1.0 mg/kg), meperidine (0.3-10.0 mg/kg) and normeperidine (1.0-17.0 mg/kg) produced dose-related decreases in rates of responding and produced small changes in the temporal pattern of responding in monkeys not tolerant to morphine. Food- and shock-maintained responding generally were affected similarly. Naloxone (0.1-3.0 mg/kg) had no effect when given alone to nontolerant monkeys. Both morphine tolerance and naloxone administration reversed the rate-decreasing effects of morphine and shifted the morphine dose-effect function to the right. Naloxone administration and morphine tolerance also reversed the rate-decreasing effects of meperidine and normeperidine, but unlike with morphine, combinations of naloxone and meperidine or normeperidine disrupted temporal patterns of responding and, at the higher doses, increased rates of responding well above control values. Drug effects in morphine-tolerant or naloxone-treated monkeys were not dependent on the event maintaining responding as comparable local rates of responding maintained by food or shock presentation were affected similarly. It was concluded that meperidine and normeperidine possess behavioral effects in common with those of morphine as well as pronounced non-morphine-like effects which are revealed by interference with the receptors upon which morphine acts.

摘要

在食物或电击呈现的多重固定间隔5分钟、固定间隔5分钟的时间表下,维持吗啡耐受和非耐受松鼠猴的杠杆按压反应。在多重时间表下,5分钟间隔后的首次反应根据当时的刺激产生食物或电击。由食物或电击维持的反应的特点是在5分钟间隔内呈正加速反应模式。吗啡(0.1 - 1.0毫克/千克)、哌替啶(0.3 - 10.0毫克/千克)和去甲哌替啶(1.0 - 17.0毫克/千克)使未耐受吗啡的猴子的反应率产生剂量相关的下降,并使反应的时间模式产生微小变化。食物和电击维持的反应通常受到类似影响。单独给未耐受的猴子注射纳洛酮(0.1 - 3.0毫克/千克)没有效果。吗啡耐受和纳洛酮给药都能逆转吗啡的反应率降低作用,并使吗啡剂量效应函数向右移动。纳洛酮给药和吗啡耐受也能逆转哌替啶和去甲哌替啶的反应率降低作用,但与吗啡不同的是,纳洛酮与哌替啶或去甲哌替啶的组合会破坏反应的时间模式,并且在较高剂量时,反应率会增加到远高于对照值。吗啡耐受或纳洛酮处理的猴子的药物效应不依赖于维持反应的事件,因为由食物或电击呈现维持的可比局部反应率受到类似影响。得出的结论是,哌替啶和去甲哌替啶具有与吗啡相同的行为效应以及明显的非吗啡样效应,这些效应通过干扰吗啡作用的受体而显现出来。

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