M. R. C. Clinical Pharmacology Research group, Department of Clinical Pharmacology, Royal Postgraduate Medical School, London.
Br J Clin Pharmacol. 1974 Apr;1(2):113-8. doi: 10.1111/j.1365-2125.1974.tb00219.x.
1 Methods for the investigation of possible interactions with tricyclic antidepressant drugs are described. These methods have been applied to a new compound, Ciba 34276-Ba, which has been shown to have antidepressant activity. 2 In five normal volunteers tested before and during treatment with Ciba 34276-Ba, no abnormalities of resting or post-exercise electrocardiographs occurred. A three-fold reduction in tyramine-responsiveness was seen in three normal subjects studied, but no potentiation of the noradrenaline pressor effect occurred. One of six patients given Ciba 34276-Ba whilst on long-term treatment with bethanidine showed loss of blood pressure control. 3 The metabolic clearance of antipyrine was unaltered in two subjects studied, showing no evidence of induction or inhibition of hepatic microsomal oxidizing enzymes by Ciba 34276-Ba.
描述了研究与三环类抗抑郁药可能相互作用的方法。这些方法已应用于一种具有抗抑郁活性的新化合物,即汽巴 34276-Ba。
在五名接受汽巴 34276-Ba 治疗前后的正常志愿者中,静息或运动后心电图无异常。在研究的 3 名正常受试者中,发现去甲肾上腺素反应性降低了三倍,但去甲肾上腺素升压作用没有增强。在六名接受汽巴 34276-Ba 治疗的患者中,有 1 名在长期接受贝那替嗪治疗时出现血压控制丧失。
在两名受试者中,安替比林的代谢清除率没有改变,表明汽巴 34276-Ba 没有诱导或抑制肝微粒体氧化酶。