Dextromethorphan as a potential rapid-acting antidepressant

被引:46
作者
Lauterbach, Edward C. [1 ,2 ]
机构
[1] Mercer Univ, Sch Med, Dept Psychiat & Behav Sci, Macon, GA 31201 USA
[2] Mercer Univ, Sch Med, Neurol Sect, Dept Internal Med, Macon, GA 31201 USA
关键词
METHYL-D-ASPARTATE; PSYCHOTIC MAJOR DEPRESSION; INTRAVENOUS KETAMINE TEST; NMDA/GLUTAMATE MECHANISM; ANTAGONIST; MAGNESIUM; MEMANTINE; NMDA; ASSOCIATION; INHIBITION;
D O I
10.1016/j.mehy.2011.02.003
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Dextromethorphan shares pharmacological properties in common with antidepressants and, in particular, ketamine, a drug with demonstrated rapid-acting antidepressant activity. Pharmacodynamic similarities include actions on NMDA, mu. opiate, sigma-1, calcium channel, serotonin transporter, and muscarinic sites. Additional unique properties potentially contributory to an antidepressant effect include actions at beta, alpha-2, and serotonin1b/d receptors. It is therefore, hypothesized that dextromethorphan may have antidepressant efficacy in bipolar, unipolar, major depression, psychotic, and treatment-resistant depressive disorders, and may display rapid-onset of antidepressant response. An antidepressant response may be associated with a positive family history of alcoholism, prediction of ketamine response, increased AMPA-to-NMDA receptor activity ratio, antidepressant properties in animal models of depression, reward system activation, enhanced erythrocyte magnesium concentration, and correlation with frontal mu receptor binding potential. Clinical trials of dextromethorphan in depressive disorders, especially treatment-resistant depression, now seem warranted. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:717 / 719
页数:3
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