Rampello L, Nicoletti G, Raffaele R, Drago F
Institute of Neurological Sciences, University of Catania, School of Medicine, Italy.
Neuropsychobiology. 1995;31(3):130-4. doi: 10.1159/000119183.
In a double-blind, placebo-controlled study, the therapeutic efficacy of two antidepressants with different neurochemical mechanisms of action, amitriptyline and amineptine, was investigated in patients affected by anxious depression. Sixty-six patients with the primary diagnosis of major depression or bipolar affective disorder (DSM-III-R) and meeting additional operational clinical criteria such as anxiety, trepidation, restlessness, early and/or late insomnia, impulsivity, hostility, dysphoria, compulsivity, hyperperspiration, palpitation, pollakiuria and phobias were included. They were randomly assigned to three groups (n = 22) and treated either with placebo, amitriptyline (up to 100 mg/day) or amineptine (up to 200 mg/day) for 6 weeks. Patients showed better response to amitriptyline, a preferential inhibitor of serotonin reuptake, than to amineptine, a selective inhibitor of dopamine reuptake. The present results suggest that alterations in serotonergic rather than dopaminergic transmission contribute to the pathophysiology of anxious depression.
在一项双盲、安慰剂对照研究中,对两种具有不同神经化学作用机制的抗抑郁药——阿米替林和阿密曲替林,在患有焦虑性抑郁症的患者中进行了治疗效果研究。纳入了66例初步诊断为重度抑郁症或双相情感障碍(DSM-III-R)且符合其他操作性临床标准的患者,如焦虑、惊恐、烦躁不安、早醒和/或晚睡性失眠、冲动、敌意、烦躁、强迫行为、多汗、心悸、尿频和恐惧症。他们被随机分为三组(每组n = 22),并分别接受安慰剂、阿米替林(最大剂量100毫克/天)或阿密曲替林(最大剂量200毫克/天)治疗6周。与多巴胺再摄取选择性抑制剂阿密曲替林相比,患者对5-羟色胺再摄取优先抑制剂阿米替林的反应更好。目前的结果表明,血清素能而非多巴胺能传递的改变促成了焦虑性抑郁症的病理生理过程。