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喷他佐辛、环唑辛和烯丙吗啡作为辨别刺激物。

Pentazocine, cyclazocine, and nalorphine as discriminative stimuli.

作者信息

Hirschhorn I D

出版信息

Psychopharmacology (Berl). 1977 Nov 15;54(3):289-94. doi: 10.1007/BF00426578.

Abstract

Pentazocine, cyclazocine, and nalorphine are narcotic antagonists that also have analgesic activity of their own. The present investigation compared the stimulus properties of these three drugs in rats. Each drug was used as a discriminative stimulus for a separate group of rats. Depression of one lever resulted in food reinforcement following the administration of drug, and the opposite lever was reinforced after saline. Each drug readily acquired control of discriminated responding. The specific narcotic antagonist, naloxone, which antagonizes many of the effects of pentazocine, cyclazocine, and nalorphine, also antagonized the discrimination of these drugs. Stimulus generalization tests to each other narcotic antagonist, d-amphetamine, morphine, and LSD, showed that each narcotic antagonist has highly specific stimulus properties. Clear generalization occurred only to pentazocine and cyclazocine in the nalorphine-saline group, but neither cyclazocine nor pentazocine generalized to nalorphine.

摘要

喷他佐辛、环佐辛和烯丙吗啡是具有自身镇痛活性的麻醉拮抗剂。本研究比较了这三种药物在大鼠体内的刺激特性。每种药物分别用于一组大鼠作为辨别刺激物。按下一个杠杆会在给药后得到食物强化,而按下另一个杠杆在注射生理盐水后得到强化。每种药物都很容易获得对辨别反应的控制。特异性麻醉拮抗剂纳洛酮可拮抗喷他佐辛、环佐辛和烯丙吗啡的许多作用,它也能拮抗对这些药物的辨别。对其他麻醉拮抗剂、右旋苯丙胺、吗啡和麦角酸二乙酰胺进行的刺激泛化试验表明,每种麻醉拮抗剂都具有高度特异性的刺激特性。在烯丙吗啡-生理盐水组中,仅对喷他佐辛和环佐辛有明显的泛化,但环佐辛和喷他佐辛都不会泛化到烯丙吗啡。

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