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安他拉明,一种假定的促肾上腺皮质激素释放激素受体1拮抗剂,对恒河猴有短暂的强化作用。

Antalarmin, a putative CRH-RI antagonist, has transient reinforcing effects in rhesus monkeys.

作者信息

Broadbear Jillian H, Winger Gail, Rice Kenner C, Woods James H

机构信息

Department of Pharmacology, University of Michigan, Ann Arbor 48109-0632, USA.

出版信息

Psychopharmacology (Berl). 2002 Nov;164(3):268-76. doi: 10.1007/s00213-002-1187-y. Epub 2002 Sep 5.

Abstract

RATIONALE

During the course of our investigation of antalarmin, a corticotropin-releasing hormone (CRH) antagonist, in rhesus monkeys, we noticed that large, intravenous doses of antalarmin resulted in behavioral changes that resembled intoxication.

OBJECTIVES

Antalarmin was evaluated in rhesus monkeys for its reinforcing effectiveness as well as for its effects on hypothalamic-pituitary-adrenal (HPA) axis activity.

METHODS

Twelve monkeys, each with a surgically implanted indwelling venous catheter, were trained to respond for and receive the short-acting barbiturate, methohexital. Monkeys responded on one of two schedules: a fixed ratio (FR) 10 (30 or 100), timeout (TO) 10 s schedule on which they received methohexital, antalarmin, vehicle or saline injections; or an FR30, TO 45 s during which saline, vehicle, or four different doses of methohexital or antalarmin were available. Each dose was available during a 25-min period separated by a 10-min TO. Blood samples were obtained from three monkeys before, during and after the self-administration sessions and assayed for ACTH and cortisol.

RESULTS

Antalarmin initially served as a reinforcer in 11 of 12 monkeys, although its reinforcing effects dissipated after three to four exposures under both operant schedules. Self-injection of antalarmin did not produce any change in cortisol levels, although methohexital did attenuate ACTH and cortisol release.

CONCLUSIONS

This study provides the first evidence for transient reinforcing properties of a putative centrally acting CRH-R1 selective antagonist.

摘要

原理

在我们对恒河猴进行促肾上腺皮质激素释放激素(CRH)拮抗剂安他拉美(antalarmin)的研究过程中,我们注意到静脉注射大剂量的安他拉美会导致类似中毒的行为变化。

目的

在恒河猴中评估安他拉美的强化效果及其对下丘脑 - 垂体 - 肾上腺(HPA)轴活性的影响。

方法

12只恒河猴,每只都通过手术植入了留置静脉导管,训练它们对短效巴比妥类药物美索比妥做出反应并接受该药物。猴子按照以下两种程序之一做出反应:一种是固定比率(FR)10(30或100),超时(TO)10秒的程序,在此程序中它们接受美索比妥、安他拉美、赋形剂或生理盐水注射;另一种是FR30,TO 45秒,在此期间可获得生理盐水、赋形剂或四种不同剂量的美索比妥或安他拉美。每个剂量在25分钟的时间段内可用,中间间隔10分钟的TO。在自我给药前、给药期间和给药后从三只猴子采集血样,并检测促肾上腺皮质激素(ACTH)和皮质醇。

结果

安他拉美最初在12只猴子中的11只中起到了强化物的作用,尽管在两种操作程序下,经过三到四次接触后其强化作用消失。自我注射安他拉美并未使皮质醇水平发生任何变化,尽管美索比妥确实减弱了ACTH和皮质醇的释放。

结论

本研究为一种假定的中枢作用CRH-R1选择性拮抗剂的短暂强化特性提供了首个证据。

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