首页> 美国卫生研究院文献>Psychopharmacology Bulletin >Treatment Resistant Depression with Loss of Antidepressant Response: Rapid—Acting Antidepressant Action of Dextromethorphan A Possible Treatment Bridging Molecule
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Treatment Resistant Depression with Loss of Antidepressant Response: Rapid—Acting Antidepressant Action of Dextromethorphan A Possible Treatment Bridging Molecule

机译:抗抑郁反应丧失的抗治疗性抑郁症:右美沙芬的速效抗抑郁作用一种可能的治疗桥联分子

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摘要

Dextromethorphan (DM) may have ketamine—like rapid—acting, treatment—resistant, and conventional antidepressant effects., This reports our initial experience with DM in unipolar Major Depressive Disorder (MDD). A patient with treatment—resistant MDD (failing adequate trials of citalopram and vortioxetine) with loss of antidepressant response (to fluoxetine and bupropion) twice experienced a rapid—acting antidepressant effect within 48 hours of DM administration and lasting 7 days, sustained up to 20 days with daily administration, then gradually developing labile loss of antidepressant response over the ensuing 7 days. Upon full relapse in DSM-5 MDD while taking 600 mg/day of the strong CYP2D6 inhibitor bupropion XL, a 300 mg oral loading dose of DM was given, followed by 60 mg po bid after an additional dose—finding period, without side effects. DM exhibited a ketamine—like rapid—acting antidepressant effect, thought to be mediated by mTOR activation (related to NMDA PCP site antagonism, sigma-1 and beta adrenergic receptor stimulation) and 5HTT inhibition, resulting in AMPA receptor trafficking, and dendritogenesis, spinogenesis, synaptogenesis, and increased neuronal survival (related to NMDA antagonism and sigma-1 and mTOR signaling). This report appears to be the first report of a rapid—acting effect in unipolar MDD and adds to antidepressant effects observed in the retrospective chart review of 77 patients with Bipolar II Disorder (Kelly and Lieberman 2014). If replicated, there is some reason to think that the administration of other agents with DM, such as lithium or D-cycloserine, might prolong the duration of the rapid-antidepressant effect.
机译:右美沙芬(DM)可能具有氯胺酮,如速效,抗药性和常规抗抑郁作用。这报告了我们在单相严重抑郁症(MDD)中使用DM的初步经验。患有抗药性MDD(西酞普兰和伏替西汀的充分试验失败)且抗抑郁药反应(对氟西汀和安非他酮)丧失的患者在DM给药48小时内持续7天经历了快速的抗抑郁药作用,持续长达20天每天服用1天,然后在随后的7天内逐渐发展出不稳定的抗抑郁药反应。当在DSM-5 MDD中完全复发并同时服用600 mg /天的强效CYP2D6抑制剂安非他酮XL时,给予300 mg口服DM口服剂量,随后在追加剂量后60 mg po bid-查找期,无副作用。 DM表现出氯胺酮(如速效)一样的抗抑郁作用,被认为是由mTOR激活(与NMDA PCP位点拮抗作用,sigma-1和β肾上腺素能受体刺激有关)和5HTT抑制介导的,导致AMPA受体运输,树突形成,自旋发生,突触发生和神经元存活增加(与NMDA拮抗作用以及sigma-1和mTOR信号传导有关)。该报告似乎是单相MDD迅速起效的第一份报告,并增加了对77例Bipolar II障碍患者的回顾性图表回顾中观察到的抗抑郁作用(Kelly和Lieberman 2014)。如果被复制,则有理由认为,将其他药物与DM一起给药(例如锂或D-环丝氨酸)可能会延长快速抗抑郁药作用的持续时间。

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