Recent developments in the psychobiology and pharmacotherapy of depression: optimising existing treatments and novel approaches for the future

被引:20
作者
Farvolden, P
Kennedy, SH
Lam, RW
机构
[1] Ctr Addict & Mental Hlth, Toronto, ON M5T 1R8, Canada
[2] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[3] Univ British Columbia, Univ Hlth Network, Vancouver, BC V5Z 1M9, Canada
[4] Univ British Columbia, Dept Psychiat, Vancouver, BC, Canada
[5] Dept Clin Res, Toronto, ON M5T 1R8, Canada
关键词
affective disorders; agonists; antagonists; antiglucocorticoids; benzodiazepines; brain-derived neurotrophic factor; corticotropin-releasing factor; dopamine; depression; GABA; glutamate; monoamine oxidase inhibitors; neuropeptides; nicotine; noradrenaline; psychopharmacology; serotonin blockers; serotonin re-uptake inhibitors; serotonin; substance P; treatment; tropic factors;
D O I
10.1517/13543784.12.1.65
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Effective antidepressants include monoamine oxiclase inhibitors and tricyclic antidepressants, selective serotonin re-uptake inhibitors and novel agents, including serotonin and noradrenaline re-uptake inhibitors. Although effective, current treatments most often produce partial symptomatic improvement (response) rather than symptom resolution and optimal functioning (remission). While current pharmacotherapies target monoaminergic systems, different symptoms of major depressive disorder (MDD) may have distinct neurobiological underpinnings and other neurobiological systems are likely involved in the pathogenesis of MDD. In this article a review of current pharmacotherapeutic options for MDD, current understanding of the neurobiology and pathogenesis of MDD and a review of new and promising directions in pharmacological research will be provided. It is generally accepted that no single neurotransmitter or system is responsible for the dysregulation found in MDD. While agents that affect monoaminergic systems will likely continue to be first-line treatments for MDD for the foreseeable future, a number of new and novel agents, including corticotropin-releasing factor antagonists, substance P antagonists and antiglucocorticoids show considerable promise for refining treatment options. In order to better understand the neurobiology and treatment response of MDD, it is probable that more sophisticated theory-driven typologies of MDD will have to be developed.
引用
收藏
页码:65 / 86
页数:22
相关论文
共 266 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]  
AMSTERDAM JP, 2000, M 40 ANN NEW CLIN DR, P15
[3]  
Anderson I M, 1998, Depress Anxiety, V7 Suppl 1, P11, DOI 10.1002/(SICI)1520-6394(1998)7:1+<11::AID-DA4>3.3.CO
[4]  
2-O
[5]   Selective serotonin reuptake inhibitors versus tricyclic antidepressants: a meta-analysis of efficacy and tolerability [J].
Anderson, IM .
JOURNAL OF AFFECTIVE DISORDERS, 2000, 58 (01) :19-36
[6]   THE EFFICACY OF SELECTIVE SEROTONIN REUPTAKE INHIBITORS IN DEPRESSION - A METAANALYSIS OF STUDIES AGAINST TRICYCLIC ANTIDEPRESSANTS [J].
ANDERSON, IM ;
TOMENSON, BM .
JOURNAL OF PSYCHOPHARMACOLOGY, 1994, 8 (04) :238-249
[7]   Central 5-HT2A and D-2 dopamine receptor occupancy after sublingual administration of ORG 5222 in healthy men [J].
Andree, B ;
Halldin, C ;
VrijmoeddeVries, M ;
Farde, L .
PSYCHOPHARMACOLOGY, 1997, 131 (04) :339-345
[8]   EFFICACY OF MOCLOBEMIDE IN DIFFERENT PATIENT GROUPS - A METAANALYSIS OF STUDIES [J].
ANGST, J ;
STABL, M .
PSYCHOPHARMACOLOGY, 1992, 106 :S109-S113
[9]   Triiodothyronine augmentation in the treatment of refractory depression - A meta-analysis [J].
Aronson, R ;
Offman, HJ ;
Joffe, RT ;
Naylor, CD .
ARCHIVES OF GENERAL PSYCHIATRY, 1996, 53 (09) :842-848
[10]  
AUERBACH SB, 1995, N-S ARCH PHARMACOL, V352, P597