• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Depression, antidepressants, and peripheral blood components.

作者信息

Fisar Zdenek, Raboch Jirí

机构信息

Department of Psychiatry, 1st Faculty of Medicine, Charles University, Prague, Czech Republic.

出版信息

Neuro Endocrinol Lett. 2008 Feb;29(1):17-28.

PMID:18283265
Abstract

The biological attributes of affective disorders and factors which are able to predict a response to treatment with antidepressants have not been identified sufficiently. A number of biochemical variables in peripheral blood constituents have been tested for this purpose, as a consequence of the lack of availability of human brain tissue. At first, the biological attributes of mental disorders were sought at the level of concentrations of neurotransmitters and their metabolites or precursors. Later on, attention shifted to receptor systems. Since the 1990s, intracellular processes influenced by an illness or its treatment with psychopharmaceuticals have been at the forefront of interest. Interest in biological predictors of treatment with antidepressants has reappeared in recent years, thanks to new laboratory techniques which make it possible to monitor cellular processes associated with the transmission of nerve signals in the brain. These processes can also be studied in plasma and blood elements, especially lymphocytes and platelets. The selection of the qualities to which attention is paid can be derived from today's most widely discussed biochemical hypotheses of affective disorders, especially the monoamine hypothesis and the molecular and cellular theory of depression. Mitochondrial enzymes can also play an important role in the pathophysiology of depression and the effects of antidepressants. In this paper, we sum up the cellular, neurochemical, neuroendocrine, genetic, and neuroimmunological qualities which can be measured in peripheral blood and which appear to be indicators of affective disorders, or parameters which make it possible to predict therapeutic responses to antidepressant administration.

摘要

相似文献

1
Depression, antidepressants, and peripheral blood components.
Neuro Endocrinol Lett. 2008 Feb;29(1):17-28.
2
[Neuroplasticity and depression].[神经可塑性与抑郁症]
Psychiatr Hung. 2005;20(1):4-17.
3
[Predictors of prophylactic response to lithium].[锂预防性反应的预测因素]
Encephale. 2008 Sep;34(4):394-9. doi: 10.1016/j.encep.2007.05.002. Epub 2007 Nov 26.
4
[Somatic and biological factors predicting a response to antidepressive agents].
Encephale. 1991 Dec;17 Spec No 3:387-90.
5
The therapeutic potential of the endocannabinoid system for the development of a novel class of antidepressants.内源性大麻素系统在开发新型抗抑郁药方面的治疗潜力。
Trends Pharmacol Sci. 2009 Sep;30(9):484-93. doi: 10.1016/j.tips.2009.06.006. Epub 2009 Sep 3.
6
[Advances in the molecular treatment of depression].[抑郁症分子治疗的进展]
Rev Neurol. 2003;37(5):459-70.
7
[Biomarkers of depression].[抑郁症的生物标志物]
Rev Neurol. 2010 Apr 16;50(8):470-6.
8
Antiapoptotic and neurotrophic effects of antidepressants: a review of clinical and experimental studies.抗抑郁药的抗凋亡和神经营养作用:临床与实验研究综述
Brain Res Bull. 2009 Jun 30;79(5):248-57. doi: 10.1016/j.brainresbull.2009.03.009. Epub 2009 Apr 5.
9
[Affective disorders and antidepressant drugs: Therapeutic innovations].[情感障碍与抗抑郁药物:治疗创新]
Encephale. 2010 Dec;36 Suppl 6:S183-7. doi: 10.1016/S0013-7006(10)70055-5.
10
Therapeutic implication of cocaine- and amphetamine-regulated transcript (CART) in the treatment of depression.可卡因和苯丙胺调节转录物(CART)在抑郁症治疗中的治疗意义。
Med Hypotheses. 2007;69(1):132-5. doi: 10.1016/j.mehy.2006.11.009. Epub 2006 Dec 29.

引用本文的文献

1
Investigating aberrantly expressed microRNAs in peripheral blood mononuclear cells from patients with treatment‑resistant schizophrenia using miRNA sequencing and integrated bioinformatics.采用 miRNA 测序和综合生物信息学方法研究治疗抵抗性精神分裂症患者外周血单个核细胞中异常表达的 microRNAs。
Mol Med Rep. 2020 Nov;22(5):4340-4350. doi: 10.3892/mmr.2020.11513. Epub 2020 Sep 15.
2
MicroRNA-Based Biomarkers in the Diagnosis and Monitoring of Therapeutic Response in Patients with Depression.基于微小RNA的生物标志物在抑郁症患者诊断及治疗反应监测中的应用
Neuropsychiatr Dis Treat. 2019 Dec 27;15:3583-3597. doi: 10.2147/NDT.S237116. eCollection 2019.
3
Co-Expression Network Analysis Revealed That the Gene Is Associated With Major Depressive Disorder.
共表达网络分析表明该基因与重度抑郁症有关。
Front Genet. 2019 Aug 2;10:703. doi: 10.3389/fgene.2019.00703. eCollection 2019.
4
exerts an antidepressive effect by downregulating miR-124 and releasing inhibition of the MAPK14 and Gria3 signaling pathways.通过下调miR-124并解除对MAPK14和Gria3信号通路的抑制来发挥抗抑郁作用。
Neural Regen Res. 2018 May;13(5):837-845. doi: 10.4103/1673-5374.232478.
5
The Neurobiology of Depression: an Integrated Overview from Biological Theories to Clinical Evidence.抑郁症的神经生物学:从生物学理论到临床证据的综合概述。
Mol Neurobiol. 2017 Sep;54(7):4847-4865. doi: 10.1007/s12035-016-0032-y. Epub 2016 Aug 10.
6
Risk assessment and predicting outcomes in patients with depressive symptoms: a review of potential role of peripheral blood based biomarkers.抑郁症状患者的风险评估与预后预测:基于外周血生物标志物潜在作用的综述
Front Hum Neurosci. 2015 Feb 2;9:18. doi: 10.3389/fnhum.2015.00018. eCollection 2015.
7
Altered microRNA Expression in Peripheral Blood Mononuclear Cells from Young Patients with Schizophrenia.精神分裂症年轻患者外周血单个核细胞中微小RNA表达的改变
J Mol Neurosci. 2015 Jul;56(3):562-71. doi: 10.1007/s12031-015-0503-z. Epub 2015 Feb 11.
8
Trajectories of depression severity in clinical trials of duloxetine: insights into antidepressant and placebo responses.度洛西汀临床试验中抑郁严重程度的轨迹:对抗抑郁药和安慰剂反应的见解
Arch Gen Psychiatry. 2011 Dec;68(12):1227-37. doi: 10.1001/archgenpsychiatry.2011.132.
9
Regulation of glycogen synthase kinase-3 during bipolar mania treatment.双相情感障碍治疗期间糖原合酶激酶-3 的调节。
Bipolar Disord. 2010 Nov;12(7):741-52. doi: 10.1111/j.1399-5618.2010.00866.x.