Litvinova S V, Kozlov A Iu, Kaliuzhnyĭ L V
Biull Eksp Biol Med. 1993 Jul;116(7):54-6.
In morphine-sensitive (s.c. 1.5 mg/kg) Wistar rats (60%) i.p. inoculation of 300-600 mg/kg d-Phenylalanine (d-Pha) did not change the nociception (tail-flick test), but in morphine-resistant rats (40%) evoked a dose-dependent analgetic effect. In morphine-sensitive rats (40%) chronic morphine administration induced the tolerance and d-Pha injection evoked analgetic effect. Morphine injection just after d-Pha analgesia was over evoked analgetic effect in morphine-resistant and -tolerant rats. It is suggested that morphine-resistant rats have a congenital and morphine-tolerant rats an acquired high level of enkephalinase activity which blocked the morphine analgetic action.
在对吗啡敏感(皮下注射1.5毫克/千克)的Wistar大鼠(60%)中,腹腔注射300 - 600毫克/千克的d - 苯丙氨酸(d - Pha)不会改变伤害感受(甩尾试验),但在对吗啡耐药的大鼠(40%)中会引起剂量依赖性的镇痛作用。在对吗啡敏感的大鼠(40%)中,长期给予吗啡会诱导耐受性,而注射d - Pha会产生镇痛作用。在d - Pha镇痛作用结束后立即注射吗啡,会在对吗啡耐药和耐受的大鼠中引起镇痛作用。提示对吗啡耐药的大鼠具有先天性的,而对吗啡耐受的大鼠具有后天获得的高水平脑啡肽酶活性,这会阻断吗啡的镇痛作用。