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社交恐惧症的心理药理学治疗:选择性单胺氧化酶-A抑制剂溴法罗明的临床及生化效应

Psychopharmacological treatment of social phobia: clinical and biochemical effects of brofaromine, a selective MAO-A inhibitor.

作者信息

van Vliet I M, den Boer J A, Westenberg H G

机构信息

Department of Biological Psychiatry, Academic Hospital Utrecht, The Netherlands.

出版信息

Eur Neuropsychopharmacol. 1992 Mar;2(1):21-9. doi: 10.1016/0924-977x(92)90032-4.

Abstract

There is circumstantial evidence that antidepressants, particularly monoamine oxidase inhibitors (MAOIs) and beta-blockers, may have some beneficial effects in social phobia. In this study 30 patients with social phobia (DSM-IIIR) were treated with the selective and reversible MAO-A inhibitor brofaromine, using a 12-week double-blind placebo controlled design. A clinical relevant improvement was seen in 80% of the patients treated with brofaromine (150 mg daily). A significant improvement was found on measures of social anxiety, phobic avoidance, general (or anticipatory) anxiety and interpersonal sensitivity in patients on brofaromine, but not on placebo. Biochemical measurements revealed a decrease in turnover of noradrenaline, serotonin and dopamine as assessed by the plasma metabolite levels, and an increase in nocturnal release of melatonin. Most prominent side-effect was middle sleep disturbance. No changes in blood pressure were observed. During a follow-up period of 12 weeks a further improvement was found in patients treated with brofaromine.

摘要

有间接证据表明,抗抑郁药,尤其是单胺氧化酶抑制剂(MAOIs)和β受体阻滞剂,可能对社交恐惧症有一些有益效果。在本研究中,采用为期12周的双盲安慰剂对照设计,对30例社交恐惧症(DSM-IIIR)患者使用选择性可逆MAO-A抑制剂溴法罗明进行治疗。接受溴法罗明(每日150毫克)治疗的患者中,80%出现了临床相关改善。在接受溴法罗明治疗的患者中,社交焦虑、恐惧回避、一般(或预期)焦虑和人际敏感性测量指标有显著改善,但安慰剂组未见改善。生化测量显示,通过血浆代谢物水平评估,去甲肾上腺素、血清素和多巴胺的周转率下降,褪黑素夜间释放增加。最突出的副作用是中度睡眠障碍。未观察到血压变化。在为期12周的随访期内,接受溴法罗明治疗的患者有进一步改善。

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