Papeschi R, Theiss P, Ayhan H
Psychopharmacologia. 1976 Mar 16;46(2):149-57. doi: 10.1007/BF00421384.
Acute morphine induced a dose-dependent hypokinesia and rigidity, but only mild and non-dose-dependent catalepsy. AMT, injected 1/2 h after morphine, slightly potentiated catalepsy but not hypokinesia during 3 h after morphine; in contrast, rigidity was decreased. The behavioral changes induced by AMT were accelerated in onset and reached their usual development, although AMT toxicity and hypothermia were completely antagonized; thus, it would appear that AMT hypokinesia/catalepsy are not the consequence of toxicity. When morphine was injected 4 h after AMT, a mutual potentiation of the two drugs on hypokinesia and catalepsy was observed, although previous biochemical measurements had shown no effect of morphine on CA depletion under these conditions. Rigidity appeared to be antagonized. After 17 days of repeated injections, morphine no longer elicited hypokinesia and catalepsy, but no cross-tolerance developed to the AMT behavioral changes. A similar lack of cross-tolerance to the effects of AMT or haloperidol was observed when morphine tolerance was induced by pellet implantation. Catalepsy and hypokinesia developed in a much more pronounced way after two large i.p. doses than after small, multiple administration of AMT; this difference was accompanied by a significantly lower concentration of brain DA, but not NA in the former group. The hyperthermic response observed after a 40 mg/kg s.c. injection of morphine was reversed to hypothermia when the same dose was given 4 or 10 h after CA synthesis inhibition. Cocaine strongly antagonized AMT hypokinesia and catalepsy when given 8 1/2 h after AMT, and, although to a lesser extent, even when injected 12 1/2 h after AMT.
急性给予吗啡可引起剂量依赖性运动减少和强直,但仅引起轻度且非剂量依赖性的僵住症。在吗啡给药后1/2小时注射AMT,在吗啡给药后的3小时内,AMT可轻微增强僵住症,但对运动减少无影响;相反,强直症状减轻。尽管AMT的毒性和体温过低完全被拮抗,但AMT诱导的行为变化起效加快并达到其通常的发展程度;因此,AMT引起的运动减少/僵住症似乎不是毒性的结果。当在AMT给药后4小时注射吗啡时,观察到两种药物对运动减少和僵住症有相互增强作用,尽管先前的生化测量表明在这些条件下吗啡对儿茶酚胺(CA)耗竭没有影响。强直症状似乎被拮抗。重复注射17天后,吗啡不再引起运动减少和僵住症,但对AMT引起的行为变化未产生交叉耐受性。当通过植入药丸诱导吗啡耐受性时,观察到对AMT或氟哌啶醇的作用同样缺乏交叉耐受性。与多次小剂量给予AMT相比,两次大剂量腹腔注射后,僵住症和运动减少的症状更为明显;这种差异伴随着前一组中脑多巴胺(DA)浓度显著降低,但去甲肾上腺素(NA)浓度未降低。当在CA合成抑制后4或10小时给予相同剂量的吗啡时,皮下注射40mg/kg吗啡后观察到的体温过高反应转变为体温过低。当在AMT给药后8.5小时给予可卡因时,可卡因可强烈拮抗AMT引起的运动减少和僵住症,即使在AMT给药后12.5小时注射,可卡因也有一定程度的拮抗作用,尽管作用程度较小。