Hiramatsu M, Inoue K
Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Meijo University, 150 Yagotoyama, Tenpaku-ku, Nagoya, Japan.
Eur J Pharmacol. 2000 Apr 28;395(2):149-56. doi: 10.1016/s0014-2999(00)00162-x.
The effects of fmol doses of nociceptin/orphanin FQ on scopolamine-induced impairment of learning and/or memory were examined using spontaneous alternation of Y-maze and step-down type passive avoidance tasks. While fmol doses of nociceptin alone had no effect on spontaneous alternation or passive avoidance behavior in normal mice, administration of nociceptin (10 and/or 100 fmol/mouse) 30 min before spontaneous alternation performance or the training session of the passive avoidance task, significantly improved the scopolamine-induced impairment of spontaneous alternation and passive avoidance behavior. This ameliorating effect was not antagonized by nocistatin (0.5 and 5.0 nmol/mouse, i.c.v.), naloxone benzoylhydrazone (2.3, 11.2, and 56.1 micromol/kg, s.c.) or nor-binaltorphimine (4.9 nmol/mouse, i.c.v.). These results indicated that very low doses of nociceptin ameliorate impairments of spontaneous alternation and passive avoidance induced by scopolamine, and suggested that this peptide has bidirectional modulatory effects on learning and memory; impairment at high doses and amelioration at low doses.
使用Y迷宫自发交替和逐步下降型被动回避任务,研究了飞摩尔剂量的孤啡肽/孤啡肽FQ对东莨菪碱诱导的学习和/或记忆损害的影响。虽然飞摩尔剂量的孤啡肽单独对正常小鼠的自发交替或被动回避行为没有影响,但在自发交替表现或被动回避任务训练前30分钟给予孤啡肽(10和/或100飞摩尔/小鼠),可显著改善东莨菪碱诱导的自发交替和被动回避行为损害。这种改善作用不受镇痛素(0.5和5.0纳摩尔/小鼠,脑室内注射)、纳洛酮苯甲酰腙(2.3、11.2和56.1微摩尔/千克,皮下注射)或去甲二丙诺啡(4.9纳摩尔/小鼠,脑室内注射)的拮抗。这些结果表明,极低剂量的孤啡肽可改善东莨菪碱诱导的自发交替和被动回避损害,并提示该肽对学习和记忆具有双向调节作用;高剂量时损害,低剂量时改善。