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纳洛酮不能拮抗苯环己哌啶对大鼠垂体-肾上腺轴的刺激作用。

Naloxone does not antagonize PCP-induced stimulation of the pituitary-adrenal axis in the rat.

作者信息

Pechnick R N, George R, Poland R E

机构信息

Department of Pharmacology, UCLA School of Medicine 90024-1735.

出版信息

Life Sci. 1989;44(2):143-7. doi: 10.1016/0024-3205(89)90532-8.

Abstract

Phencyclidine (PCP) has been shown to stimulate the pituitary-adrenal axis in the rat. The purpose of the present study was to determine whether opiate receptors are involved in this effect by testing whether pretreatment with the opiate antagonist naloxone can antagonize PCP-induced ACTH and corticosterone release. PCP (10.0 mg/kg) produced increases in plasma ACTH and corticosterone 60 min after s.c. administration. Pretreatment with naloxone (2.0 mg/kg s.c.) did not reduce the rise in plasma levels of ACTH or corticosterone produced by PCP. These results indicate that naloxone-sensitive opiate receptors are not involved in the PCP-induced stimulation of the pituitary-adrenal axis in rats.

摘要

苯环己哌啶(PCP)已被证明可刺激大鼠的垂体-肾上腺轴。本研究的目的是通过测试用阿片拮抗剂纳洛酮预处理是否能拮抗PCP诱导的促肾上腺皮质激素(ACTH)和皮质酮释放,来确定阿片受体是否参与了这一效应。皮下注射PCP(10.0mg/kg)后60分钟,血浆ACTH和皮质酮水平升高。用纳洛酮(2.0mg/kg皮下注射)预处理并未降低PCP引起的血浆ACTH或皮质酮水平的升高。这些结果表明,纳洛酮敏感的阿片受体不参与PCP诱导的大鼠垂体-肾上腺轴的刺激。

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