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Agomelatine: Antidepressant with a New Mechanism of Action / 대한정신약물학회지
Article in Ko | WPRIM | ID: wpr-78815
Responsible library: WPRO
ABSTRACT
Currently available pharmacotherapies for depression still have a limited antidepressant efficacy with a delayed onset of several weeks, and still cause side effects. These unmet needs represent important reasons to continue to search for novel treatment options. A disorganization of circadian rhythms has been suggested to play an important role in the pathophysiology of major depression. Agomelatine is a new agent with a unique pharmacological profile. Agomelatine is both an agonist of melatonergic MT(1) and MT(2) receptors and a serotonergic 5-HT(2C) receptor antagonist. Many clinical trials have demonstrated the superior efficacy of agomelatine in comparison with placebo in the treatment major depressive disorder at the standard dose of 25 mg/day, with the possibility of increasing doses to 50 mg/day in those patients with insufficient improvement. Agomelatine was even effective in severely depressed patients. The safety and tolerability of agomelatine was comparable to placebo. It does not induce the side effects including serotonin syndrome and sexual dysfunction or discontinuation syndrome typical to other therapies, such as selective serotonin reuptake inhibitors. These properties give agomelatine a definite clinical advantage in the treatment of depression.
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Full text: 1 Index: WPRIM Main subject: Circadian Rhythm / Selective Serotonin Reuptake Inhibitors / Serotonin Syndrome / Receptor, Serotonin, 5-HT2C / Depression / Depressive Disorder, Major / Imidazoles / Acetamides / Nitro Compounds Type of study: Clinical_trials Limits: Humans Language: Ko Journal: Korean Journal of Psychopharmacology Year: 2009 Type: Article
Full text: 1 Index: WPRIM Main subject: Circadian Rhythm / Selective Serotonin Reuptake Inhibitors / Serotonin Syndrome / Receptor, Serotonin, 5-HT2C / Depression / Depressive Disorder, Major / Imidazoles / Acetamides / Nitro Compounds Type of study: Clinical_trials Limits: Humans Language: Ko Journal: Korean Journal of Psychopharmacology Year: 2009 Type: Article