Zarate Carlos A, Singh Jaskaran B, Quiroz Jorge A, De Jesus Georgette, Denicoff Kirk K, Luckenbaugh David A, Manji Husseini K, Charney Dennis S
Mood and Anxiety Disorders Program, National Institute of Mental Health, Department of Human Health Services, Bethesda, MD, USA.
Am J Psychiatry. 2006 Jan;163(1):153-5. doi: 10.1176/appi.ajp.163.1.153.
This study was designed to assess possible antidepressant effects of memantine, a selective N-methyl-D-aspartate (NMDA) receptor antagonist in humans.
In a double-blind, placebo-controlled study, 32 subjects with major depression were randomly assigned to receive memantine (5-20 mg/day) (N=16) or placebo (N=16) for 8 weeks. Primary efficacy was assessed by performance on the Montgomery-Asberg Depression Rating Scale (MADRS).
The linear mixed models for total MADRS scores showed no treatment effect.
In an 8-week trial, the low-to-moderate-affinity NMDA antagonist memantine in doses of 5-20 mg/day was not effective in the treatment of major depressive disorder.
本研究旨在评估美金刚(一种选择性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂)对人类可能的抗抑郁作用。
在一项双盲、安慰剂对照研究中,32名重度抑郁症患者被随机分配接受美金刚(5-20毫克/天)(N=16)或安慰剂(N=16)治疗8周。主要疗效通过蒙哥马利-阿斯伯格抑郁评定量表(MADRS)的表现进行评估。
MADRS总分的线性混合模型显示无治疗效果。
在一项为期8周的试验中,剂量为5-20毫克/天的低至中等亲和力NMDA拮抗剂美金刚对重度抑郁症无效。