GLYX-13, an NMDA receptor glycine site functional partial agonist enhances cognition and produces antidepressant effects without the psychotomimetic side effects of NMDA receptor antagonists

被引:130
作者
Moskal, Joseph R. [1 ]
Burch, Ronald [2 ]
Burgdorf, Jeffrey S. [1 ]
Kroes, Roger A. [1 ]
Stanton, Patric K. [3 ]
Disterhoft, John F. [1 ]
Leander, J. David [2 ]
机构
[1] Northwestern Univ, McCormick Sch Engn & Appl Sci, Falk Ctr Mol Therapeut, Dept Biomed Engn, Evanston, IL 60201 USA
[2] Naurex Inc, Evanston, IL USA
[3] New York Med Coll, Dept Cell Biol & Anat, Valhalla, NY 10595 USA
关键词
antidepressant; depression; glycine site; major depressive disorder; NMDA receptor; rapid-acting; METHYL-D-ASPARTATE; LONG-TERM POTENTIATION; TARGETED POINT MUTATIONS; PROTEIN-KINASE-II; SYNAPTIC PLASTICITY; MONOCLONAL-ANTIBODY; D-CYCLOSERINE; HIPPOCAMPAL-NEURONS; SUBUNIT COMPOSITION; PREFRONTAL CORTEX;
D O I
10.1517/13543784.2014.852536
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: The N-methyl-D-aspartate receptor-ionophore complex plays a key role in learning and memory and has efficacy in animals and humans with affective disorders. GLYX-13 is an N-methyl-D-aspartate receptor (NMDAR) glycine-site functional partial agonist and cognitive enhancer that also shows rapid antidepressant activity without psychotomimetic side effects. Areas covered: The authors review the mechanism of action of GLYX-13 that was investigated in preclinical studies and evaluated in clinical studies. Specifically, the authors review its pharmacology, pharmacokinetics, and drug safety that were demonstrated in clinical studies. Expert opinion: NMDAR full antagonists can produce rapid antidepressant effects in treatment-resistant subjects; however, they are often accompanied by psychotomimetic effects that make chronic use outside of a clinical trial inpatient setting problematic. GLYX-13 appears to exert its antidepressant effects in the frontal cortex via NMDAR-triggered synaptic plasticity. Understanding the mechanistic underpinning of GLYX-13's antidepressant action should provide both novel insights into the role of the glutamatergic system in depression and identify new targets for therapeutic development.
引用
收藏
页码:243 / 254
页数:12
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