Botting R, Bower S, Eason C T, Hutson P H, Wells L
J Pharm Pharmacol. 1978 Jan;30(1):36-40. doi: 10.1111/j.2042-7158.1978.tb13149.x.
A single injection of phenelzine 100 mg kg-1 given 18 h before, decreased the analgesia and hypothermia induced by morphine, but potentiated the analgesic and hypothermic effects of pethidine, when the analgesics were administered either intraperitoneally, or intracerebroventricularly. The modification of pethidine analgesia and hypothermia, but not morphine analgesia, was antagonized by methysergide (10 mg lg-1, s.c.). The LD50 of pethidine, but not that of morphine, was 30-40% lower in mice treated with phenelzine tranylcypromine or iproniazid 6 h before the test. The increased lethality of a single dose of pethidine induced by phenelzine was also prevented by methysergide. Pretreatment of mice with 100 mg kg-1 phenelzine was followed by a significant rise in both brain tryptophan and 5-hydroxytryptamine (5-HT) concentrations which lasted for 24 h. Therefore, the changes in pethidine effects could have been due to raised brain tryptophan and 5-HT concentrations.
在镇痛剂腹腔注射或脑室内注射前18小时给予100毫克/千克的单剂量苯乙肼,可降低吗啡诱导的镇痛和体温过低,但增强哌替啶的镇痛和体温过低作用。麦角新碱(10毫克/千克,皮下注射)可拮抗哌替啶镇痛和体温过低的改变,但不拮抗吗啡镇痛的改变。在测试前6小时用苯乙肼、反苯环丙胺或异烟肼处理的小鼠中,哌替啶的半数致死量降低了30 - 40%,而吗啡的半数致死量未降低。麦角新碱也可预防苯乙肼诱导的单剂量哌替啶致死率增加。用100毫克/千克苯乙肼预处理小鼠后,脑色氨酸和5 - 羟色胺(5 - HT)浓度均显著升高,且持续24小时。因此,哌替啶作用的改变可能是由于脑色氨酸和5 - HT浓度升高所致。