Suppr超能文献

血清素相关通路与发育可塑性:对精神疾病的相关性

Serotonin-related pathways and developmental plasticity: relevance for psychiatric disorders.

作者信息

Dayer Alexandre

机构信息

Departments of Mental Health and Psychiatry and Basic Neurosciences, University of Geneva Medical School, Geneva, Switzerland.

出版信息

Dialogues Clin Neurosci. 2014 Mar;16(1):29-41. doi: 10.31887/DCNS.2014.16.1/adayer.

Abstract

Risk for adult psychiatric disorders is partially determined by early-life alterations occurring during neural circuit formation and maturation. In this perspective, recent data show that the serotonin system regulates key cellular processes involved in the construction of cortical circuits. Translational data for rodents indicate that early-life serotonin dysregulation leads to a wide range of behavioral alterations, ranging from stress-related phenotypes to social deficits. Studies in humans have revealed that serotonin-related genetic variants interact with early-life stress to regulate stress-induced cortisol responsiveness and activate the neural circuits involved in mood and anxiety disorders. Emerging data demonstrate that early-life adversity induces epigenetic modifications in serotonin-related genes. Finally, recent findings reveal that selective serotonin reuptake inhibitors can reinstate juvenile-like forms of neural plasticity, thus allowing the erasure of long-lasting fear memories. These approaches are providing new insights on the biological mechanisms and clinical application of antidepressants.

摘要

成人精神疾病的风险部分由神经回路形成和成熟过程中发生的早期生命改变所决定。从这个角度来看,最近的数据表明,血清素系统调节参与皮质回路构建的关键细胞过程。啮齿动物的转化数据表明,早期生命中的血清素失调会导致广泛的行为改变,从与压力相关的表型到社交缺陷。对人类的研究表明,与血清素相关的基因变异与早期生命压力相互作用,以调节压力诱导的皮质醇反应性,并激活参与情绪和焦虑障碍的神经回路。新出现的数据表明,早期生命逆境会诱导血清素相关基因的表观遗传修饰。最后,最近的研究结果表明,选择性血清素再摄取抑制剂可以恢复类似幼年的神经可塑性形式,从而消除长期的恐惧记忆。这些方法为抗抑郁药的生物学机制和临床应用提供了新的见解。

相似文献

1
Serotonin-related pathways and developmental plasticity: relevance for psychiatric disorders.
Dialogues Clin Neurosci. 2014 Mar;16(1):29-41. doi: 10.31887/DCNS.2014.16.1/adayer.
2
Long-Term Impact of Early-Life Stress on Hippocampal Plasticity: Spotlight on Astrocytes.
Int J Mol Sci. 2020 Jul 15;21(14):4999. doi: 10.3390/ijms21144999.
3
Early life adversity shapes neural circuit function during sensitive postnatal developmental periods.
Transl Psychiatry. 2022 Aug 1;12(1):306. doi: 10.1038/s41398-022-02092-9.
4
GPCR signaling: role in mediating the effects of early adversity in psychiatric disorders.
FEBS J. 2021 Apr;288(8):2602-2621. doi: 10.1111/febs.15738. Epub 2021 Feb 16.
5
Excess of serotonin affects neocortical pyramidal neuron migration.
Transl Psychiatry. 2011 Oct 11;1(10):e47. doi: 10.1038/tp.2011.49.
6
[Neurogenesis. Relevance for pathophysiology and pharmacotherapy of psychiatric diseases].
Nervenarzt. 2005 Jan;76(1):11-9. doi: 10.1007/s00115-004-1775-7.
7
Interaction between BDNF and serotonin: role in mood disorders.
Neuropsychopharmacology. 2008 Jan;33(1):73-83. doi: 10.1038/sj.npp.1301571. Epub 2007 Sep 19.
8
Long-term effects of early environment on the brain: Lesson from rodent models.
Semin Cell Dev Biol. 2018 May;77:81-92. doi: 10.1016/j.semcdb.2017.09.039. Epub 2017 Oct 7.
10
Rodent models of social stress and neuronal plasticity: Relevance to depressive-like disorders.
Behav Brain Res. 2019 Sep 2;369:111900. doi: 10.1016/j.bbr.2019.111900. Epub 2019 Apr 22.

引用本文的文献

1
Wiring and Volume Transmission: An Overview of the Dual Modality for Serotonin Neurotransmission.
ACS Chem Neurosci. 2023 Dec 6;14(23):4093-4104. doi: 10.1021/acschemneuro.3c00648. Epub 2023 Nov 15.
2
Anxiety and depression: A top-down, bottom-up model of circuit function.
Ann N Y Acad Sci. 2023 Jul;1525(1):70-87. doi: 10.1111/nyas.14997. Epub 2023 May 2.
3
Increased left dorsolateral prefrontal cortex density following escitalopram intake during relearning: a randomized, placebo-controlled trial in healthy humans.
Ther Adv Psychopharmacol. 2022 Nov 17;12:20451253221132085. doi: 10.1177/20451253221132085. eCollection 2022.
6
9
Role of the Serotonin Receptor 7 in Brain Plasticity: From Development to Disease.
Int J Mol Sci. 2020 Jan 13;21(2):505. doi: 10.3390/ijms21020505.

本文引用的文献

3
Childhood maltreatment and methylation of the glucocorticoid receptor gene NR3C1 in bipolar disorder.
Br J Psychiatry. 2014 Jan;204(1):30-5. doi: 10.1192/bjp.bp.112.120055. Epub 2013 Jun 6.
4
High rate of disease-related copy number variations in childhood onset schizophrenia.
Mol Psychiatry. 2014 May;19(5):568-72. doi: 10.1038/mp.2013.59. Epub 2013 May 21.
6
Genetic and epigenetic associations of MAOA and NR3C1 with depression and childhood adversities.
Int J Neuropsychopharmacol. 2013 Aug;16(7):1513-28. doi: 10.1017/S1461145713000102. Epub 2013 Mar 1.
7
Postnatal growth defects in mice with constitutive depletion of central serotonin.
ACS Chem Neurosci. 2013 Jan 16;4(1):171-81. doi: 10.1021/cn300165x. Epub 2012 Dec 15.
9
Perseverative instrumental and Pavlovian responding to conditioned stimuli in serotonin transporter knockout rats.
Neurobiol Learn Mem. 2013 Feb;100:48-55. doi: 10.1016/j.nlm.2012.12.004. Epub 2012 Dec 20.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验