首页> 外文期刊>European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology >Can we increase speed and efficacy of antidepressant treatments? Part I: General aspects and monoamine-based strategies
【24h】

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

机译:我们可以提高抗抑郁药物治疗的速度和功效吗? 第一部分:一般方面和基于单胺的策略

获取原文
获取原文并翻译 | 示例
           

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.
机译:主要抑郁症(MDD)是一种严重的精神综合征,具有普及率和社会经济影响。目前的抗抑郁药物基于血清素(5-羟基特胺,5-HT)和/或去甲肾上腺素转运蛋白的阻断。这些药物表现出临床作用和有限功效的缓慢发作,部分原因是由于通过吸入器(5-HT1A,5-HT1B,Alpha(2) - α(2) - Regectors)和后腹膜受体(例如,5 -ht3)。因此,临床相关剂量的再摄取抑制剂在中脑中核细胞中增加了细胞外(活性)5-HT浓度,但不在前脑中,如啮齿动物微透露研究和灵长类动物/人脑中的PET扫描研究所示。通过上述受体的拮抗剂预防这些自我抑制机制增加了临床前和临床抗抑郁作用。因此,混合的β-肾上腺素依赖者/ 5-HT1A拮抗剂己烯醇加速,在某些情况下,增强了选择性血清素再摄取抑制剂(SSRI)的临床作用。该策略已被纳入两种新的多目标抗抑郁药物,维尔唑酮和涡旋葡萄酒,其在5-HT1A受体中结合了5-Ht再摄取抑制和部分激动。 Vortioxetine表现出对其他5-HT受体的高亲和力,包括位于皮质和海马GABA中间核中的兴奋性5-HT3受体。 Vortioxetine的5-HT3受体阻断增强了前额叶皮质的金字塔神经元活性以及皮质和海马5-HT释放。知道这些新的抗抑郁药是否会代表现有世界中现有药物的真正进展仍然是至早的。然而,他们的发展基于防止衰减单胺活性的局部和远端自我抑制机制,对未来的抗抑郁药物开辟了道路。 (c)2017 Elsevier B.V.和ECNP。版权所有。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号