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多种阿片受体参与大鼠不同苯环利定诱导的非条件性行为的证据。

Evidence for multiple opiate receptor involvement in different phencyclidine-induced unconditioned behaviors in rats.

作者信息

Greenberg B D, Segal D S

出版信息

Psychopharmacology (Berl). 1986;88(1):44-53. doi: 10.1007/BF00310511.

DOI:10.1007/BF00310511
PMID:3003779
Abstract

Rats were used for comparing the behavioral response profiles of phencyclidine (PCP) and d,1-N-allylnormetazocine (NANM), two drugs that are proposed to exert their effects through the "PCP/sigma" receptor. Phencyclidine (1.0-5.0 mg/kg) and NANM (2.5-10.0 mg/kg) induced dose-related increases in locomotion, sniffing, repetitive head movements, non-object directed mouth movements, and ataxia. Both drugs also increased food and water consumption during the latter portion of the drug response. Ingestive behaviors induced by PCP (2.5 mg/kg), as with eating and drinking stimulated by the mu-opiate morphine (2.0 mg/kg), were blocked by a relatively low dose of the opiate antagonist naloxone (0.5 mg/kg). Multiple injections of PCP (2.5 mg/kg for 4 days) or NANM (10.0 mg/kg for 4 days) augmented several measures of behavioral activation, including horizontal locomotion, rearing, and nonfocused sniffing, but did not significantly change stereotyped behaviors or ataxia. Reciprocal cross-sensitization of locomotor activation is indicated by the finding that the response to a challenge injection of PCP (2.5 mg/kg) or to NANM (10.0 mg/kg) after 4 days of treatment with the other drug closely resembled the enhanced locomotor response observed after the chronic treatment. Phencyclidine and NANM thus appear to exert many of their effects on unconditioned behavior through common mechanisms, including interaction with sigma receptors. In addition, these findings are consistent with previous suggestions that a mu-opiate receptor system may modulate some effects of PCP.

摘要

选用大鼠来比较苯环利定(PCP)和d,1-N-烯丙基去甲左啡诺(NANM)的行为反应特征,这两种药物被认为是通过“PCP/σ”受体发挥作用的。苯环利定(1.0 - 5.0毫克/千克)和NANM(2.5 - 10.0毫克/千克)可引起与剂量相关的运动增加、嗅探、重复性头部运动、非目标指向性口部运动和共济失调。两种药物还会在药物反应后期增加食物和水的摄入量。PCP(2.5毫克/千克)诱导的摄食行为,就像μ-阿片类吗啡(2.0毫克/千克)刺激的进食和饮水行为一样,会被相对低剂量的阿片拮抗剂纳洛酮(0.5毫克/千克)阻断。多次注射PCP(2.5毫克/千克,共4天)或NANM(10.0毫克/千克,共4天)可增强多种行为激活指标,包括水平运动、竖毛和非聚焦嗅探,但不会显著改变刻板行为或共济失调。对另一种药物进行4天治疗后,对PCP(2.5毫克/千克)或NANM(10.0毫克/千克)激发注射的反应与慢性治疗后观察到的增强运动反应非常相似,这一发现表明存在运动激活的交叉致敏作用。因此,苯环利定和NANM似乎通过共同机制对非条件行为产生许多影响,包括与σ受体的相互作用。此外,这些发现与之前关于μ-阿片受体系统可能调节PCP某些作用的观点一致。

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本文引用的文献

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Multiple daily amphetamine administration: behavioral and neurochemical alterations.多次每日安非他命给药:行为和神经化学改变。
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Effects of naloxone, metenkephalin, and morphine on phencyclidine-induced behavior in the rat.纳洛酮、甲硫脑啡肽和吗啡对大鼠苯环己哌啶诱导行为的影响。
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