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本文引用的文献

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Elevated tph2 mRNA expression in a rat model of chronic anxiety.慢性焦虑大鼠模型中 tph2 mRNA 表达升高。
Depress Anxiety. 2012 Apr;29(4):307-19. doi: 10.1002/da.21925.
2
Effects of continuously enhanced corticotropin releasing factor expression within the bed nucleus of the stria terminalis on conditioned and unconditioned anxiety.终纹床核内持续增强的促肾上腺皮质释放因子表达对条件性和非条件性焦虑的影响。
Mol Psychiatry. 2013 Mar;18(3):308-19. doi: 10.1038/mp.2011.188. Epub 2012 Jan 31.
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5-HT and mechanisms of defence.5-羟色胺与防御机制
J Psychopharmacol. 1991 Jan;5(4):305-15. doi: 10.1177/026988119100500414.
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Projections and interconnections of genetically defined serotonin neurons in mice.在小鼠中,遗传定义的血清素神经元的投射和连接。
Eur J Neurosci. 2012 Jan;35(1):85-96. doi: 10.1111/j.1460-9568.2011.07936.x. Epub 2011 Dec 13.
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Development of raphe serotonin neurons from specification to guidance.中缝核 5-羟色胺神经元的发育:从特化到导向。
Eur J Neurosci. 2011 Nov;34(10):1553-62. doi: 10.1111/j.1460-9568.2011.07910.x.
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Uncontrollable, but not controllable, stress desensitizes 5-HT1A receptors in the dorsal raphe nucleus.无法控制但并非不可控制的压力会使中缝背核的 5-HT1A 受体脱敏。
J Neurosci. 2011 Oct 5;31(40):14107-15. doi: 10.1523/JNEUROSCI.3095-11.2011.
7
Swim stress activates serotonergic and nonserotonergic neurons in specific subdivisions of the rat dorsal raphe nucleus in a temperature-dependent manner.游泳应激以温度依赖的方式激活大鼠中缝背核特定亚区的 5-羟色胺能和非 5-羟色胺能神经元。
Neuroscience. 2011 Dec 1;197:251-68. doi: 10.1016/j.neuroscience.2011.09.011. Epub 2011 Sep 16.
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Development by environment interactions controlling tryptophan hydroxylase expression.环境相互作用控制色氨酸羟化酶表达的发展。
J Chem Neuroanat. 2011 Jul;41(4):219-26. doi: 10.1016/j.jchemneu.2011.05.002. Epub 2011 May 25.
9
Shifting topographic activation and 5-HT1A receptor-mediated inhibition of dorsal raphe serotonin neurons produced by nicotine exposure and withdrawal.尼古丁暴露和戒断引起的背缝核 5-羟色胺神经元的拓扑激活和 5-HT1A 受体介导的抑制作用的改变。
Eur J Neurosci. 2011 May;33(10):1866-75. doi: 10.1111/j.1460-9568.2011.07677.x. Epub 2011 Apr 19.
10
A genetically defined morphologically and functionally unique subset of 5-HT neurons in the mouse raphe nuclei.在小鼠中,5-HT 神经元在基因上定义、形态上和功能上独特的亚群。
J Neurosci. 2011 Feb 23;31(8):2756-68. doi: 10.1523/JNEUROSCI.4080-10.2011.

与应激相关的 5-羟色胺能系统:对焦虑和情感障碍症状学的影响。

Stress-related serotonergic systems: implications for symptomatology of anxiety and affective disorders.

机构信息

School of Psychological Science, La Trobe University, Melbourne, Australia.

出版信息

Cell Mol Neurobiol. 2012 Jul;32(5):695-708. doi: 10.1007/s10571-012-9827-1. Epub 2012 Apr 7.

DOI:10.1007/s10571-012-9827-1
PMID:22484834
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3378822/
Abstract

Previous studies have suggested that serotonergic neurons in the midbrain raphe complex have a functional topographic organization. Recent studies suggest that stimulation of a bed nucleus of the stria terminalis-dorsal raphe nucleus pathway by stress- and anxiety-related stimuli modulates a subpopulation of serotonergic neurons in the dorsal part of the dorsal raphe nucleus (DRD) and caudal part of the dorsal raphe nucleus (DRC) that participates in facilitation of anxiety-like responses. In contrast, recent studies suggest that activation of a spinoparabrachial pathway by peripheral thermal or immune stimuli excites subpopulations of serotonergic neurons in the ventrolateral part of the dorsal raphe nucleus/ventrolateral periaqueducal gray (DRVL/VLPAG) region and interfascicular part of the dorsal raphe nucleus (DRI). Studies support a role for serotonergic neurons in the DRVL/VLPAG in inhibition of panic-like responses, and serotonergic neurons in the DRI in antidepressant-like effects. Thus, data suggest that while some subpopulations of serotonergic neurons in the dorsal raphe nucleus play a role in facilitation of anxiety-like responses, others play a role in inhibition of anxiety- or panic-like responses, while others play a role in antidepressant-like effects. Understanding the anatomical and functional properties of these distinct serotonergic systems may lead to novel therapeutic strategies for the prevention and/or treatment of affective and anxiety disorders. In this review, we describe the anatomical and functional properties of subpopulations of serotonergic neurons in the dorsal raphe nucleus, with a focus on those implicated in symptoms of anxiety and affective disorders, the DRD/DRC, DRVL/VLPAG, and DRI.

摘要

先前的研究表明,中脑中缝核复合体中的 5-羟色胺能神经元具有功能上的拓扑组织。最近的研究表明,应激和焦虑相关刺激对终纹床核-中缝背核通路的刺激调节了中缝背核(DRD)背侧部和尾部(DRC)的一个亚群 5-羟色胺能神经元,这些神经元参与促进焦虑样反应。相比之下,最近的研究表明,外周热或免疫刺激对中缝背核腹外侧部/腹外侧导水管周围灰质(DRVL/VLPAG)区域和中缝背核间束部(DRI)的 5-羟色胺能神经元亚群的激活,由脊髓-脑桥旁通路的激活引起。研究支持 DRVL/VLPAG 中的 5-羟色胺能神经元在抑制惊恐样反应中的作用,以及 DRI 中的 5-羟色胺能神经元在抗抑郁样效应中的作用。因此,数据表明,虽然中缝背核中的一些 5-羟色胺能神经元亚群在促进焦虑样反应中起作用,但其他亚群在抑制焦虑或惊恐样反应中起作用,而其他亚群在抗抑郁样效应中起作用。了解这些不同的 5-羟色胺能系统的解剖和功能特性可能会导致预防和/或治疗情感和焦虑障碍的新的治疗策略。在这篇综述中,我们描述了中缝背核中 5-羟色胺能神经元亚群的解剖和功能特性,重点介绍了与焦虑和情感障碍症状有关的亚群,即 DRD/DRC、DRVL/VLPAG 和 DRI。