Tulunay F C, Jen M F, Chang J K, Loh H H, Lee N M
Eur J Pharmacol. 1981 Dec 3;76(2-3):235-9. doi: 10.1016/0014-2999(81)90506-9.
Pretreatment of mice with a single injection of morphine, beta-endorphin, Leu-enkephalin, FK33824 or [D-Ala2-D-Leu5]enkephalin, for 3 h increased the ability of naloxone to antagonize the analgesic effects of morphine. However, dynorphin-(1-13) can only antagonize morphine, beta-endorphin or Leu-enkephalin induced increased naloxone efficacy but not FK33824 or [D-Ala2-D-Leu2]enkephalin. Dynorphin itself can also increase naloxone efficacy when treated alone. However, this effect can be prevented when animals are pretreated with dynorphin and naloxone together.
单次注射吗啡、β-内啡肽、亮氨酸脑啡肽、FK33824或[D-丙氨酸2-D-亮氨酸5]脑啡肽对小鼠进行预处理3小时,可增强纳洛酮拮抗吗啡镇痛作用的能力。然而,强啡肽-(1-13)只能拮抗吗啡、β-内啡肽或亮氨酸脑啡肽诱导的纳洛酮效能增加,而不能拮抗FK33824或[D-丙氨酸2-D-亮氨酸2]脑啡肽。强啡肽单独处理时也可增加纳洛酮效能。然而,当动物同时用强啡肽和纳洛酮预处理时,这种作用可被阻止。