Can we increase speed and efficacy of antidepressant treatments? Part I: General aspects and monoamine-based strategies

被引:77
作者
Artigas, Francesc [1 ,2 ,3 ]
Bortolozzi, Analia [1 ,2 ,3 ]
Celada, Pau [1 ,2 ,3 ]
机构
[1] CSIC, Inst Invest Biomed Barcelona, Dept Neurochem & Neuropharmacol, Barcelona, Spain
[2] CIBERSAM Ctr Invest Biomed Red Salud Mental, Barcelona, Spain
[3] Inst Invest Biomed August Pi & Sunyer IDIBAPS, Barcelona, Spain
关键词
5-hydroxytryptamine (serotonin) receptors; Antidepressant drugs; Autoreceptors; Multi-target agents; SEROTONIN REUPTAKE INHIBITORS; MAJOR DEPRESSIVE DISORDER; DEEP-BRAIN-STIMULATION; QUANTITATIVE ENZYME AUTORADIOGRAPHY; 5-HT1A RECEPTOR ANTAGONIST; MEDIAL PREFRONTAL CORTEX; OF-ONSET DISTRIBUTIONS; MIDBRAIN RAPHE NUCLEI; STAR-ASTERISK-D; RAT-BRAIN;
D O I
10.1016/j.euroneuro.2017.10.032
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Major depressive disorder (MDD) is a severe psychiatric syndrome with high prevalence and socioeconomic impact. Current antidepressant treatments are based on the blockade of serotonin (5-hydroxytryptamine, 5-HT) and/or noradrenaline transporters. These drugs show slow onset of clinical action and limited efficacy, partly due to the activation of physiological negative feed-back mechanisms operating through autoreceptors (5-HT1A, 5-HT1B, alpha(2)-adrenoceptors) and postsynaptic receptors (e.g., 5-HT3 ). As a result, clinically-relevant doses of reuptake inhibitors increase extracellular (active) 5-HT concentrations in the midbrain raphe nuclei but not in forebrain, as indicated by rodent microdialysis studies and by PET-scan studies in primate/human brain. The prevention of these self-inhibitory mechanisms by antagonists of the above receptors augments preclinical and clinical antidepressant effects. Hence, the mixed beta-adrenoceptor/5-HT1A antagonist pindolol accelerated, and in some cases enhanced, the clinical action of selective serotonin reuptake inhibitors (SSRI). This strategy has been incorporated into two new multi-target antidepressant drugs, vilazodone and vortioxetine, which combine 5-HT reuptake inhibition and partial agonism at 5-HT1A receptors. Vortioxetine shows also high affinity for other 5-HT receptors, including excitatory 5-HT3 receptors located in cortical and hippocampal GABA interneurons. 5-HT3 receptor blockade by vortioxetine enhances pyramidal neuron activity in prefrontal cortex as well as cortical and hippocampal 5-HT release. It is still too soon to know whether these new antidepressants will represent a real advance over existing drugs in the real world. However, their development opened the way to future antidepressant drugs based on the prevention of local and distal self-inhibitory mechanisms attenuating monoamine activity. (C) 2017 Elsevier B.V. and ECNP. All rights reserved.
引用
收藏
页码:445 / 456
页数:12
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