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大鼠注射乙基酮环唑新、Mr 2266和纳曲酮后苯环利定诱发的刻板行为。

Phencyclidine-induced stereotyped behaviors after injection of ethylketocyclazocine, Mr 2266 and naltrexone in rats.

作者信息

Nabeshima T, Hiramatsu M, Kameyama T

出版信息

Brain Res. 1986 Jul 23;378(2):234-9. doi: 10.1016/0006-8993(86)90926-1.

Abstract

The effects of ethylketocyclazocine (EKC), Mr 2266 and naltrexone on the stereotyped behaviors induced by an intraperitoneal injection of phencyclidine (PCP) were examined. PCP-induced turning, backpedalling, head weaving and sniffing were antagonized by pretreatment with EKC (0.25-4.0 mg/kg). While pretreatment with Mr 2266 (2.5 mg/kg), a kappa selective antagonist, and naltrexone (10 mg/kg), a mu selective antagonist, failed to affect the PCP-induced stereotypy, Mr 2266 antagonized the suppressing effect of EKC on PCP-induced stereotypy. Taken into consideration, this suggests that kappa opioid agonists such as EKC antagonize PCP-induced stereotyped behaviors through a kappa opioid mechanism, and that the mu opioid receptor may not play an important role in the PCP-induced stereotypy in rats.

摘要

研究了乙基酮环唑辛(EKC)、Mr 2266和纳曲酮对腹腔注射苯环己哌啶(PCP)诱导的刻板行为的影响。EKC(0.25 - 4.0毫克/千克)预处理可拮抗PCP诱导的旋转、倒退、头部摆动和嗅探行为。虽然κ选择性拮抗剂Mr 2266(2.5毫克/千克)和μ选择性拮抗剂纳曲酮(10毫克/千克)预处理未能影响PCP诱导的刻板行为,但Mr 2266拮抗了EKC对PCP诱导的刻板行为的抑制作用。综合考虑,这表明EKC等κ阿片类激动剂通过κ阿片类机制拮抗PCP诱导的刻板行为,并且μ阿片受体可能在大鼠PCP诱导的刻板行为中不起重要作用。

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