Kuribara H, Asami T, Ida I, Tadokoro S
Division for Behavior Analysis, Gunma University School of Medicine, Maebashi, Japan.
Jpn J Pharmacol. 1990 Nov;54(3):325-9. doi: 10.1254/jjp.54.325.
The single administration of ceruletide at 10-300 micrograms/kg, i.p., slightly but significantly decreased the response rate (frequency of shuttles) under a discrete avoidance task in mice. Over 10 micrograms/kg of ceruletide attenuated the increase in the response rate induced by methamphetamine (0.5 mg/kg, s.c.). However, ceruletide, at 1-300 micrograms/kg, did not significantly enhance the response- and/or avoidance-decreasing effects of chlorpromazine (1 mg/kg, s.c.), haloperidol (0.1 mg/kg, s.c.), pilocarpine (4 mg/kg, s.c.) and N6-(L-2-phenylisopropyl)-adenosine (0.1 mg/kg, s.c.), but rather tended to reduce the avoidance-decreasing effect of chlorpromazine and pilocarpine at 1-100 micrograms/kg.
以10 - 300微克/千克的剂量腹腔注射蛙皮素,可使小鼠在离散回避任务中的反应率(穿梭频率)略有但显著降低。蛙皮素剂量超过10微克/千克可减弱甲基苯丙胺(0.5毫克/千克,皮下注射)诱导的反应率升高。然而,1 - 300微克/千克的蛙皮素并未显著增强氯丙嗪(1毫克/千克,皮下注射)、氟哌啶醇(0.1毫克/千克,皮下注射)、毛果芸香碱(4毫克/千克,皮下注射)和N6 -(L - 2 - 苯异丙基)- 腺苷(0.1毫克/千克,皮下注射)的反应和/或回避降低作用,反而在1 - 100微克/千克时倾向于降低氯丙嗪和毛果芸香碱的回避降低作用。