Castellani S, Giannini A J, Adams P M
Psychopharmacology (Berl). 1982;78(1):76-80. doi: 10.1007/BF00470593.
The effects of naloxone, metenkephalin, and morphine were tested on phencyclidine(PCP)-induced stereotyped behaviors, ataxia, and hyperactivity in the rat. Naloxone (8 mg/kg) significantly decreased stereotypy, ataxia, and hyperactivity across all PCP doses tested (2.0, 4.0, and 6.0 mg/kg). Metenkephalin (40 micrograms/kg) and morphine (5 and 10 mg/kg) increased ataxia at the 4.0 and 6.0 mg/kg PCP doses. Stereotypy was altered by the opiates in a dose-dependent manner; enhanced by metenkephalin (40 micrograms/kg) at 2.0 mg/kg and inhibited by metenkephalin (40 micrograms/kg) and morphine (10 mg/kg) at 4.0 and 6.0 mg/kg PCP. Locomotor activity was increased by morphine (5 mg/kg) at 2 mg/kg PCP. These results suggest an involvement of central opiate receptor mechanisms in the mediation of PCP-induced behaviors in the rat.
研究了纳洛酮、甲硫脑啡肽和吗啡对苯环己哌啶(PCP)诱导的大鼠刻板行为、共济失调和多动的影响。纳洛酮(8毫克/千克)在所有测试的PCP剂量(2.0、4.0和6.0毫克/千克)下均显著降低了刻板行为、共济失调和多动。在PCP剂量为4.0和6.0毫克/千克时,甲硫脑啡肽(40微克/千克)和吗啡(5和10毫克/千克)增加了共济失调。阿片类药物以剂量依赖的方式改变刻板行为;在PCP剂量为2.0毫克/千克时,甲硫脑啡肽(40微克/千克)增强了刻板行为,而在PCP剂量为4.0和6.0毫克/千克时,甲硫脑啡肽(40微克/千克)和吗啡(10毫克/千克)抑制了刻板行为。在PCP剂量为2毫克/千克时,吗啡(5毫克/千克)增加了运动活性。这些结果表明,中枢阿片受体机制参与了PCP诱导的大鼠行为的介导。