Novel melatonin-based therapies: potential advances in the treatment of major depression

被引:229
作者
Hickie, Ian B. [1 ]
Rogers, Naomi L. [1 ,2 ]
机构
[1] Univ Sydney, Brain & Mind Res Inst, Camperdown, NSW 2050, Australia
[2] Cent Queensland Univ, Sch Management & Mkt, Inst Hlth & Social Sci Res, Mackay, Qld, Australia
基金
英国医学研究理事会;
关键词
PROLONGED-RELEASE MELATONIN; CHRONIC SLEEP RESTRICTION; DOUBLE-BLIND; LIGHT THERAPY; CIRCADIAN GENES; ANTIDEPRESSANT AGOMELATINE; AGONIST AGOMELATINE; RAMELTEON TAK-375; BODY-TEMPERATURE; MOOD DISORDERS;
D O I
10.1016/S0140-6736(11)60095-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Major depression is one of the leading causes of premature death and disability. Although available drugs are effective, they also have substantial limitations. Recent advances in our understanding of the fundamental links between chronobiology and major mood disorders, as well as the development of new drugs that target the circadian system, have led to a renewed focus on this area. In this review, we summarise the associations between disrupted chronobiology and major depression and outline new antidepressant treatment strategies that target the circadian system. In particular, we highlight agomelatine, a melatonin-receptor agonist and selective serotonergic receptor subtype (ie, 5-HT2C) antagonist that has chronobiotic, antidepressant, and anxiolytic effects. In the short-term, agomelatine has similar antidepressant efficacy to venlafaxine, fluoxetine, and sertraline and, in the longer term, fewer patients on agomelatine relapse (23.9%) than do those receiving placebo (50.0%). Patients with depression treated with agomelatine report improved sleep quality and reduced waking after sleep onset. As agomelatine does not raise serotonin levels, it has less potential for the common gastrointestinal, sexual, or metabolic side-effects that characterise many other antidepressant compounds.
引用
收藏
页码:621 / 631
页数:11
相关论文
共 105 条
  • [1] [Anonymous], AG SEARCH
  • [2] [Anonymous], NOV CLIN TRIAL RES D
  • [3] [Anonymous], VALDOXAN PRODUCT INF
  • [4] [Anonymous], AG SEARCH
  • [5] Patterns of performance degradation and restoration during sleep restriction and subsequent recovery: a sleep dose-response study
    Belenky, G
    Wesensten, NJ
    Thorne, DR
    Thomas, ML
    Sing, HC
    Redmond, DP
    Russo, MB
    Balkin, TJ
    [J]. JOURNAL OF SLEEP RESEARCH, 2003, 12 (01) : 1 - 12
  • [6] Brunner P, 2006, EUR J HISTOCHEM, V50, P311
  • [7] Melatonin and S-20098 increase REM sleep and wake-up propensity without modifying NREM sleep homeostasis
    Cajochen, C
    Krauchi, K
    Mori, D
    Graw, P
    WirzJustice, A
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1997, 272 (04) : R1189 - R1196
  • [8] CARMAN JS, 1976, AM J PSYCHIAT, V133, P1181
  • [9] Comparative efficacy and acceptability of 12 new-generation antidepressants: a multiple-treatments meta-analysis
    Cipriani, Andrea
    Furukawa, Toshiaki A.
    Salanti, Georgia
    Geddes, John R.
    Higgins, Julian P. T.
    Churchill, Rachel
    Watanabe, Norio
    Nakagawa, Atsuo
    Omori, Ichiro M.
    McGuire, Hugh
    Tansella, Michele
    Barbui, Corrado
    [J]. LANCET, 2009, 373 (9665) : 746 - 758
  • [10] Czeisler CA., 2005, PRINCIPLES PRACTICE, P375, DOI 10.1016/b0-72-160797-7/50038-0