Browne R G, Segal D S
Biol Psychiatry. 1980 Feb;15(1):77-86.
Locomotor activity of rats and mice was monitored following administration of the opiates, morphine, methadone, and etonitazene, or the opioid peptides, beta-endorphin, D-Ala2-Met5-enkephalinamide, and D-Met2-Pro5-enkephalinamide. In rats these agents produced dose-related biphasic patterns of activity consisting of an initial depression in locomotion followed by a period of hyperactivity. Intravenous administration of morphine, methadone, or etonitazene in mice produced dose-related increases in stereotyped locomotor activity. The metabolically resistant enkephalin analog, D-Met2-Pro5-enkephalinamide induced a similar pattern of effects. However, doses of beta-endorphin up to 20 mg/kg, iv, failed to elicit locomotor stimulation in mice. The similarity in the naloxone-reversible responses induced by opiates and certain opioid peptides suggests that the same underlying mechanisms may subserve their behavioral effects.
在给大鼠和小鼠施用阿片类药物(吗啡、美沙酮和依托尼嗪)或阿片肽(β-内啡肽、D-丙氨酸²-甲硫氨酸⁵-脑啡肽酰胺和D-甲硫氨酸²-脯氨酸⁵-脑啡肽酰胺)后,监测了它们的运动活性。在大鼠中,这些药物产生了与剂量相关的双相活动模式,包括最初的运动抑制,随后是一段多动期。在小鼠中静脉注射吗啡、美沙酮或依托尼嗪会产生与剂量相关的刻板运动活性增加。代谢抗性脑啡肽类似物D-甲硫氨酸²-脯氨酸⁵-脑啡肽酰胺诱导了类似的效应模式。然而,静脉注射高达20mg/kg的β-内啡肽剂量未能在小鼠中引起运动刺激。阿片类药物和某些阿片肽诱导的纳洛酮可逆反应的相似性表明,相同的潜在机制可能有助于它们的行为效应。