Literature DB >> 23876404

Quetiapine add-on therapy improves the depressive behaviors and hippocampal neurogenesis in fluoxetine treatment resistant depressive rats.

Ying Wang1, Ting Chang, Yun-Chun Chen, Rui-Guo Zhang, Hua-Ning Wang, Wen-Jun Wu, Zheng-Wu Peng, Qing-Rong Tan.   

Abstract

Quetiapine, an atypical antipsychotic, may have efficacy as augmentation therapy in treatment resistant depression (TRD), but evidence is limited and the underlying mechanism remains poorly understood. Therefore, this study was aimed to investigate whether and how quetiapine can be served as an augmentation agent in fluoxetine treatment resistant depressive rats induced by chronic unpredictable mild stress (CUMS). In this study, the effects of CUMS regimen and antidepressant treatment were assessed by behavioral tests and hippocampal neurogenesis. Approximately 20-30% of depressive rats respond poorly to fluoxetine treatment. In their hippocampus, a significant decrease of neurogenesis was also observed. However, quetiapine add-on therapy significantly improved the depressive behaviors and increased the number of the newborn neurons in the hippocampus of fluoxetine treatment resistant depressive rats. Thus, our results suggest that quetiapine may be used as an augmentation agent in the treatment resistant depression partly mediated by increasing the number of newborn neurons in the hippocampus.
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Chronic unpredictable mild stress; Hippocampus; Neurogenesis; Quetiapine; Treatment resistant depression

Mesh:

Substances:

Year:  2013        PMID: 23876404     DOI: 10.1016/j.bbr.2013.07.021

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  7 in total

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Journal:  Mol Neuropsychiatry       Date:  2019-05-21

2.  Acute and chronic treatment with quetiapine induces antidepressant-like behavior and exerts antioxidant effects in the rat brain.

Authors:  Zuleide M Ignácio; Gislaine Z Réus; Helena M Abelaira; Airam B de Moura; Thays G de Souza; Danyela Matos; Mariana P Goldim; Khiany Mathias; Leandro Garbossa; Fabricia Petronilho; João Quevedo
Journal:  Metab Brain Dis       Date:  2017-05-06       Impact factor: 3.584

Review 3.  Rodent models of treatment-resistant depression.

Authors:  Barbara J Caldarone; Venetia Zachariou; Sarah L King
Journal:  Eur J Pharmacol       Date:  2014-11-21       Impact factor: 4.432

4.  Lack of association of FKBP5 SNPs and haplotypes with susceptibility and treatment response phenotypes in Han Chinese with major depressive disorder: A pilot case-control study (STROBE).

Authors:  Chenghao Yang; Shen Li; Yanyan Ma; Bing Chen; Meijuan Li; Fokko J Bosker; Jie Li; Ilja M Nolte
Journal:  Medicine (Baltimore)       Date:  2021-09-10       Impact factor: 1.817

Review 5.  Adult Hippocampal Neurogenesis: Regulation and Possible Functional and Clinical Correlates.

Authors:  Pedro Baptista; José P Andrade
Journal:  Front Neuroanat       Date:  2018-06-05       Impact factor: 3.856

6.  Characterization of gut microbiome in mice model of depression with divergent response to escitalopram treatment.

Authors:  Jiajia Duan; Yu Huang; Xunmin Tan; Tingjia Chai; Jing Wu; Hanping Zhang; Yifan Li; Xi Hu; Peng Zheng; Ping Ji; Libo Zhao; Deyu Yang; Liang Fang; Jinlin Song; Peng Xie
Journal:  Transl Psychiatry       Date:  2021-05-20       Impact factor: 6.222

7.  Transcriptional Effects of Psychoactive Drugs on Genes Involved in Neurogenesis.

Authors:  Chiara C Bortolasci; Briana Spolding; Srisaiyini Kidnapillai; Timothy Connor; Trang T T Truong; Zoe S J Liu; Bruna Panizzutti; Mark F Richardson; Laura Gray; Michael Berk; Olivia M Dean; Ken Walder
Journal:  Int J Mol Sci       Date:  2020-11-06       Impact factor: 5.923

  7 in total

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