Psychopharmacological Agents and Suicide Risk Reduction: Ketamine and Other Approaches

被引:17
作者
Al Jurdi, Rayan K. [1 ,2 ]
Swann, Alan [1 ,2 ]
Mathew, Sanjay J. [1 ,2 ]
机构
[1] Michael E DeBakey VA Med Ctr, Houston, TX 77030 USA
[2] Baylor Coll Med, Menninger Dept Psychiat & Behav Sci, Houston, TX 77030 USA
关键词
Suicide; Ketamine; Depression; Pharmacotherapy; NMDA receptor; DEXAMETHASONE-SUPPRESSION TEST; FAILED MEDICATION TREATMENTS; RANDOMIZED CONTROLLED-TRIAL; MAJOR DEPRESSIVE DISORDER; D-ASPARTATE ANTAGONIST; ANTIDEPRESSANT EFFICACY; LITHIUM AUGMENTATION; FLUOXETINE; BEHAVIOR; BORDERLINE;
D O I
10.1007/s11920-015-0614-9
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Suicide is a major global public health problem and the leading cause of injury mortality in the USA. Suicide is a complex phenomenon involving several systems and neurobiological pathways, with interacting genetic and environmental mechanisms. The literature on the neurobiology and pharmacotherapy of suicide has been limited. To date, no medications have proven efficacious for treating acute suicidal crises. There is an emerging literature supporting a rapid anti-suicidal effect of ketamine, a non-competitive N-methyl-D-aspartate (NMDA) glutamate receptor antagonist, among depressed patients with suicidal ideation. Potential ketamine's anti-suicidal effect mechanisms are linked to interruption of the kynurenine pathway and modulating pro-inflammatory cytokines exacerbation. However, available data are not sufficient for its routine integration in clinical practice, and larger and replicated randomized control studies are needed.
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页数:10
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