Bourin M, Menez J F, Colombel M C, Larousse C
Arzneimittelforschung. 1987 May;37(5):506-9.
An isopropyl derivative of barbital (5,5-diethyl-2-(isopropyloxy)pyrimidine-4,6-dione, O2IB) was administered intraperitoneally 30 min before tests in mice. Former experimental investigations have shown that O2IB has an antidepressant psychopharmacological spectrum. It increases toxicity of yohimbine in mice at 175 mg/kg, antagonises from 50 mg/kg on hypothermia induced by a high dose of apomorphine and is active on the behavioural despair test at 125 mg/kg. These effects are those observed with classical antidepressants. Since phenytoin has an antidepressant profile in mice, carbamazepine is active on manic-depressive illness and beta-mimetic drugs are antidepressants, the question presents itself whether isopropylation or anticonvulsive activity is more important for the antidepressant psychopharmacological spectrum, or whether both are of equal importance.
在对小鼠进行测试前30分钟,腹腔注射巴比妥的异丙基衍生物(5,5 - 二乙基 - 2 -(异丙氧基)嘧啶 - 4,6 - 二酮,O2IB)。先前的实验研究表明,O2IB具有抗抑郁的精神药理谱。它在175毫克/千克时增加小鼠体内育亨宾的毒性,从50毫克/千克起拮抗高剂量阿扑吗啡诱导的体温过低,并且在125毫克/千克时对行为绝望试验有活性。这些效应是经典抗抑郁药所观察到的。由于苯妥英在小鼠中有抗抑郁特征,卡马西平对躁狂抑郁症有活性,β - 拟交感神经药物是抗抑郁药,于是出现了这样一个问题:异丙基化或抗惊厥活性对于抗抑郁精神药理谱来说哪个更重要,或者两者是否同等重要。