Comments on "an innovative design to establish proof of concept of the antidepressant effects of the NR2B subunit selective n-methyl-d-aspartate antagonist, CP-101,606, in patients with treatment-refractory major depressive disorder"
ABNORMAL BEHAVIOR;
ABNORMAL LABORATORY RESULT;
CLINICAL TRIAL;
DIZZINESS;
DRUG EFFECT;
DRUG EFFICACY;
DRUG MECHANISM;
HAMILTON SCALE;
HUMAN;
LETTER;
MAJOR DEPRESSION;
PARESTHESIA;
PRIORITY JOURNAL;
SIDE EFFECT;
SOMNOLENCE;
TREATMENT OUTCOME;
UNSPECIFIED SIDE EFFECT;
URINE ODOR;
XEROSTOMIA;
ANTIDEPRESSIVE AGENTS;
DEPRESSIVE DISORDER, MAJOR;
DOUBLE-BLIND METHOD;
DRUG RESISTANCE;
EXCITATORY AMINO ACID ANTAGONISTS;
HUMANS;
INFUSIONS, INTRAVENOUS;
PAROXETINE;
PIPERIDINES;
PSYCHIATRIC STATUS RATING SCALES;
RANDOMIZED CONTROLLED TRIALS AS TOPIC;
RECEPTORS, N-METHYL-D-ASPARTATE;
RECEPTORS, SIGMA;
RESEARCH DESIGN;
TREATMENT OUTCOME;
EID: 68449103046PISSN: 02710749EISSN: NoneSource Type: Journal DOI: 10.1097/JCP.0b013e3181ace848Document Type: Letter
An innovative design to establish proof of concept of the antidepressant effects of the NR2B subunit selective N-methyl-D-aspartate antagonist, CP-101,606, in patients with treatment-refractory major depressive disorder
Preskorn SH, Baker B, Kolluri S, et al. An innovative design to establish proof of concept of the antidepressant effects of the NR2B subunit selective N-methyl-D-aspartate antagonist, CP-101,606, in patients with treatment-refractory major depressive disorder. J Clin Psychopharmacol. 2008;28:631-637.
Targeting the glutamatergic system to develop novel, improved therapeutics for mood disorders
Sanacora G, Zarate CA, Krystal JH, et al. Targeting the glutamatergic system to develop novel, improved therapeutics for mood disorders. Nature Rev Drug Discov. 2008;7:426-437.
A randomized trial of an N-methyl-D-aspartate antagonist in treatment-resistant major depression
Zarate CA Jr, Singh JB, Carlson PJ, et al. A randomized trial of an N-methyl-D-aspartate antagonist in treatment-resistant major depression. Arch Gen Psychiatry. 2006;63:856-864.
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses
Krystal JH, Karper LP, Seibyl JP, et al. Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses. Arch Gen Psychiatry. 1994;51:199-214.
3H]ifenprodil binding site in rat brain membranes with the pharmacology of the voltage-independent ifenprodil site on N-methyl-D- aspartate receptors containing NR2B subunits
3H]ifenprodil binding site in rat brain membranes with the pharmacology of the voltage-independent ifenprodil site on N-methyl-D- aspartate receptors containing NR2B subunits. J Pharmacol Exp Ther. 2001;296:150-159.
Sigma receptor ligands: Possible application as therapeutic drugs and as radiopharmaceuticals
Hashimoto K, Ishiwata K. Sigma receptor ligands: possible application as therapeutic drugs and as radiopharmaceuticals. Curr Pharm Des. 2006;12:3857-3876.
Hashimoto K. Sigma-1 receptors and selective serotonin reuptake inhibitors: clinical implications of their relationship. CNS Agents - Med Chem. 2009; in press.
Hashimoto K. Sigma-1 receptors and selective serotonin reuptake inhibitors: clinical implications of their relationship. CNS Agents - Med Chem. 2009; in press.
* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.