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向腹侧被盖区微量注射吗啡的强化作用。

Reinforcing effects of morphine microinjection into the ventral tegmental area.

作者信息

Phillips A G, LePiane F G

出版信息

Pharmacol Biochem Behav. 1980 Jun;12(6):965-8. doi: 10.1016/0091-3057(80)90460-8.

Abstract

A neural substrate for the reinforcing property of an opiate drug was identified in the ventral tegmental area (VTA) by establishing conditioned reinforcement to salient environmental stimuli paired with intracerebral microinjections of morphine. Bilateral microinjections of morphine into the VTA in doses of 0.2 microgram and 1.0 microgram produced a subsequent change in place preference to a distinctive compartment previously associated with the stimulant effects of morphine. Microinjection of 1.0 microgram morphine at sites 2.5 mm dorsal to the VTA had no effect. Pretreatment with naloxone (2 mg/kg) antagonized the reinforcing effects of 1.0 microgram morphine as this group showed no significant change in place preference. Nor did control groups receiving microinjections of sterile physiological saline. Taken together, these data suggest that opiate receptors, located in the ventral tegmental area, play an important role in mediating the reinforcing effects of morphine. The possible involvement of dopaminergic neurons in these effects is discussed.

摘要

通过建立对与脑室内微量注射吗啡配对的显著环境刺激的条件性强化,在腹侧被盖区(VTA)中确定了阿片类药物强化特性的神经基质。以0.2微克和1.0微克的剂量向VTA双侧微量注射吗啡,随后对先前与吗啡刺激作用相关的独特隔室的位置偏好发生了变化。在VTA背侧2.5毫米处的位点微量注射1.0微克吗啡没有效果。用纳洛酮(2毫克/千克)预处理可拮抗1.0微克吗啡的强化作用,因为该组在位置偏好上没有显著变化。接受无菌生理盐水微量注射的对照组也没有变化。综上所述,这些数据表明,位于腹侧被盖区的阿片受体在介导吗啡的强化作用中起重要作用。讨论了多巴胺能神经元在这些作用中的可能参与。

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