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阿片类药物与可卡因对大鼠运动活性的相互作用:阿片类药物对μ受体的相对效能的影响

Interactions between opioids and cocaine on locomotor activity in rats: influence of an opioid's relative efficacy at the mu receptor.

作者信息

Smith Mark A, Gordon Keith A, Craig Christopher K, Bryant Paul A, Ferguson M Eric, French Adam M, Gray Jason D, McClean Jacob M, Tetirick Jonathan C

机构信息

Department of Psychology, Davidson College, NC 28035-7037, USA.

出版信息

Psychopharmacology (Berl). 2003 May;167(3):265-73. doi: 10.1007/s00213-003-1388-z. Epub 2003 Apr 1.

Abstract

RATIONALE

Cocaine and mu opioid agonists increase central dopamine concentrations and produce robust interactions at both neurochemical and behavioral levels. Although the interactions between cocaine and high-efficacy mu opioids have been well characterized, the interactions between cocaine and lower efficacy opioids have not been as extensively examined.

OBJECTIVE

The purpose of this study was to examine the interactions between cocaine and opioids possessing a range of relative efficacy at the mu receptor.

METHODS

Male, Long-Evans rats were habituated to an open-field, locomotor activity chamber, and the effects of cocaine and various opioids were tested under a cumulative dosing procedure. In this procedure, a selected dose of an opioid was administered during the first component of a session, with increasing doses of cocaine administered during subsequent components.

RESULTS

When administered alone, cocaine produced dose-dependent increases in locomotor activity that was stable across 5 weeks of behavioral testing. The high-efficacy mu opioid levorphanol, and the low-efficacy opioids buprenorphine, butorphanol, nalbuphine and (-)-pentazocine, dose-dependently enhanced the effects of cocaine at doses that did not alter locomotor activity when administered alone. In contrast, the opioid antagonist naloxone, and to a lesser extent, the kappa opioid spiradoline attenuated the effects of cocaine at doses that did not alter locomotor activity when administered alone. Across an extensive dose range, the low-efficacy opioid nalorphine failed to alter cocaine's locomotor-activating effects.

CONCLUSIONS

These data suggest that low-efficacy opioids possessing significant mu-agonist activity (e.g. buprenorphine, butorphanol, nalbuphine, (-)-pentazocine) may potentiate the effects of cocaine in a manner similar to that typically observed with high-efficacy mu opioids.

摘要

理论依据

可卡因和μ阿片受体激动剂会增加中枢多巴胺浓度,并在神经化学和行为水平上产生强烈的相互作用。尽管可卡因与高效μ阿片类药物之间的相互作用已得到充分表征,但可卡因与低效阿片类药物之间的相互作用尚未得到广泛研究。

目的

本研究的目的是研究可卡因与在μ受体上具有一系列相对效力的阿片类药物之间的相互作用。

方法

雄性朗-伊文斯大鼠适应旷场运动活动箱,并在累积给药程序下测试可卡因和各种阿片类药物的作用。在该程序中,在实验的第一部分给予选定剂量的阿片类药物,在随后的部分给予递增剂量的可卡因。

结果

单独给药时,可卡因产生剂量依赖性的运动活动增加,在5周的行为测试中保持稳定。高效μ阿片受体激动剂左啡诺,以及低效阿片类药物丁丙诺啡、布托啡诺、纳布啡和(-)-喷他佐辛,在单独给药时不改变运动活动的剂量下,剂量依赖性地增强了可卡因的作用。相比之下,阿片受体拮抗剂纳洛酮,以及在较小程度上,κ阿片受体激动剂spiradoline,在单独给药时不改变运动活动的剂量下减弱了可卡因的作用。在广泛的剂量范围内,低效阿片类药物纳洛芬未能改变可卡因的运动激活作用。

结论

这些数据表明,具有显著μ激动剂活性的低效阿片类药物(如丁丙诺啡、布托啡诺、纳布啡、(-)-喷他佐辛)可能以类似于高效μ阿片类药物通常观察到的方式增强可卡因的作用。

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