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本文引用的文献

1
Pharmacological profile of lurasidone, a novel antipsychotic agent with potent 5-hydroxytryptamine 7 (5-HT7) and 5-HT1A receptor activity.新型抗精神病药物鲁拉西酮的药理学特性,其对 5-羟色胺 7(5-HT7)受体和 5-羟色胺 1A(5-HT1A)受体具有强大的活性。
J Pharmacol Exp Ther. 2010 Jul;334(1):171-81. doi: 10.1124/jpet.110.167346. Epub 2010 Apr 19.
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Role of cortical and striatal 5-HT1A receptors in alleviating antipsychotic-induced extrapyramidal disorders.皮质和纹状体 5-HT1A 受体在缓解抗精神病药引起的锥体外系疾病中的作用。
Prog Neuropsychopharmacol Biol Psychiatry. 2010 Aug 16;34(6):877-81. doi: 10.1016/j.pnpbp.2010.04.005. Epub 2010 Apr 14.
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Lurasidone in the treatment of acute schizophrenia: a double-blind, placebo-controlled trial.鲁拉西酮治疗急性精神分裂症:一项双盲、安慰剂对照试验。
J Clin Psychiatry. 2009 Jun;70(6):829-36. doi: 10.4088/JCP.08m04905. Epub 2009 Jun 2.
4
The serotonin-1A receptor in anxiety disorders.焦虑症中的5-羟色胺-1A受体。
Biol Psychiatry. 2009 Oct 1;66(7):627-35. doi: 10.1016/j.biopsych.2009.03.012. Epub 2009 May 7.
5
Cognitive effects of antipsychotic drugs in first-episode schizophrenia and schizophreniform disorder: a randomized, open-label clinical trial (EUFEST).抗精神病药物对首发精神分裂症和精神分裂症样障碍的认知影响:一项随机、开放标签的临床试验(EUFEST)
Am J Psychiatry. 2009 Jun;166(6):675-82. doi: 10.1176/appi.ajp.2008.08060806. Epub 2009 Apr 15.
6
Effects of tandospirone, a 5-HT1A agonistic anxiolytic agent, on haloperidol-induced catalepsy and forebrain Fos expression in mice.5-HT1A 激动剂抗焦虑药坦度螺酮对小鼠氟哌啶醇诱导的僵住症及前脑 Fos 表达的影响。
J Pharmacol Sci. 2009 Apr;109(4):593-9. doi: 10.1254/jphs.08313fp. Epub 2009 Apr 7.
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Contribution of the striatum to the effects of 5-HT1A receptor stimulation in L-DOPA-treated hemiparkinsonian rats.纹状体对5-羟色胺1A受体刺激在左旋多巴治疗的偏侧帕金森病大鼠中所产生效应的作用。
J Neurosci Res. 2009 May 15;87(7):1645-58. doi: 10.1002/jnr.21978.
8
A role for the 5-HT(1A), 5-HT4 and 5-HT6 receptors in learning and memory.5-羟色胺(5-HT)1A、5-HT4和5-HT6受体在学习和记忆中的作用。
Trends Pharmacol Sci. 2008 Sep;29(9):482-92. doi: 10.1016/j.tips.2008.07.001.
9
Striatal 5-HT1A receptor stimulation reduces D1 receptor-induced dyskinesia and improves movement in the hemiparkinsonian rat.纹状体5-HT1A受体刺激可减轻D1受体诱导的异动症,并改善偏侧帕金森病大鼠的运动。
Neuropharmacology. 2008 Dec;55(8):1321-8. doi: 10.1016/j.neuropharm.2008.08.031. Epub 2008 Sep 10.
10
Does stimulation of 5-HT(1A) receptors improve cognition in schizophrenia?刺激5-羟色胺(1A)受体能否改善精神分裂症患者的认知功能?
Behav Brain Res. 2008 Dec 16;195(1):98-102. doi: 10.1016/j.bbr.2008.05.016. Epub 2008 May 29.

5-HT1A 受体在治疗精神分裂症和帕金森病中的治疗作用。

Therapeutic role of 5-HT1A receptors in the treatment of schizophrenia and Parkinson's disease.

机构信息

Laboratory of Pharmacology, Osaka University of Pharmaceutical Sciences, Nasahara, Takatsuki, Osaka, Japan.

出版信息

CNS Neurosci Ther. 2011 Feb;17(1):58-65. doi: 10.1111/j.1755-5949.2010.00211.x. Epub 2010 Nov 21.

DOI:10.1111/j.1755-5949.2010.00211.x
PMID:21091640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6493836/
Abstract

5-HT(1A) receptors have long been implicated in the pathogenesis and treatment of anxiety and depressive disorders. Recently, several lines of studies have revealed new insights into the therapeutic role of 5-HT(1A) receptors in treating schizophrenia and Parkinson's disease. Specifically, 5-HT(1A) receptors seem to be a promising target for alleviating antipsychotic-induced extrapyramidal side effects (EPS) and cognitive/affective disorders in schizophrenia. In the treatment of patients with Parkinson's disease, 5-HT(1A) agonists are expected to improve not only affective symptoms (e.g., anxiety and depression), but also the core parkinsonian symptoms as well as antiparkinsonian agents-induced side effects (e.g., L-DOPA-induced dyskinesia). Here, the therapeutic mechanisms mediated by 5-HT(1A) receptors in schizophrenia and Parkinson's disease are reviewed. This evidence should encourage discovery of new 5-HT(1A) ligands, which can resolve the unmet clinical needs in the current therapy.

摘要

5-HT(1A) 受体长期以来一直与焦虑和抑郁障碍的发病机制和治疗有关。最近,几条研究线揭示了 5-HT(1A)受体在治疗精神分裂症和帕金森病中的治疗作用的新见解。具体来说,5-HT(1A)受体似乎是缓解精神分裂症中抗精神病药引起的锥体外系副作用 (EPS) 和认知/情感障碍的有希望的靶点。在帕金森病患者的治疗中,预计 5-HT(1A)激动剂不仅能改善情感症状(如焦虑和抑郁),还能改善核心帕金森病症状以及抗帕金森病药物引起的副作用(如 L-DOPA 诱导的运动障碍)。在这里,综述了 5-HT(1A)受体在精神分裂症和帕金森病中的治疗机制。这一证据应该鼓励发现新的 5-HT(1A)配体,以解决当前治疗中未满足的临床需求。