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Comparison of LPS and MS-induced depressive mouse model: behavior, inflammation and biochemical changes

Depression is a mental disease involving complex pathophysiological mechanisms, and there are many ways to establish depressive mouse models. The purpose of this study is to comprehensively compare the behavioral changes and its mechanism induced by two different models. This study established two d...

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Autores principales: Yu, Xiaojin, Yao, Hui, Zhang, Xiaohui, Liu, Lulu, Liu, Shuangmei, Dong, Youjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443001/
https://www.ncbi.nlm.nih.gov/pubmed/36064335
http://dx.doi.org/10.1186/s12888-022-04233-2
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author Yu, Xiaojin
Yao, Hui
Zhang, Xiaohui
Liu, Lulu
Liu, Shuangmei
Dong, Youjing
author_facet Yu, Xiaojin
Yao, Hui
Zhang, Xiaohui
Liu, Lulu
Liu, Shuangmei
Dong, Youjing
author_sort Yu, Xiaojin
collection PubMed
description Depression is a mental disease involving complex pathophysiological mechanisms, and there are many ways to establish depressive mouse models. The purpose of this study is to comprehensively compare the behavioral changes and its mechanism induced by two different models. This study established two depressive mouse models by maternal separation (MS) or lipopolysaccharide (LPS) administration, and added fluoxetine treatment group respectively for comparison. MS induced more apparent anxiety-like behavior while LPS induced more apparent depressive-like behavior. LPS increased peripheral inflammatory factors more apparent, which were mitigated by fluoxetine. MS inhibited the 5-HT system more obviously and was relieved by fluoxetine. LPS triggered stronger immune response in the hippocampus and prefrontal cortex (PFC). MS significantly reduced the expression of neurotrophic proteins and was alleviated by fluoxetine. Overall, LPS induced stronger system inflammation, while MS impaired the function of HPA axis and 5-HT system. Our results will contribute to a deeper understanding of the pathophysiology of different stress-induced depression and will also help researchers select appropriate models of depression for their own needs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12888-022-04233-2.
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spelling pubmed-94430012022-09-06 Comparison of LPS and MS-induced depressive mouse model: behavior, inflammation and biochemical changes Yu, Xiaojin Yao, Hui Zhang, Xiaohui Liu, Lulu Liu, Shuangmei Dong, Youjing BMC Psychiatry Research Depression is a mental disease involving complex pathophysiological mechanisms, and there are many ways to establish depressive mouse models. The purpose of this study is to comprehensively compare the behavioral changes and its mechanism induced by two different models. This study established two depressive mouse models by maternal separation (MS) or lipopolysaccharide (LPS) administration, and added fluoxetine treatment group respectively for comparison. MS induced more apparent anxiety-like behavior while LPS induced more apparent depressive-like behavior. LPS increased peripheral inflammatory factors more apparent, which were mitigated by fluoxetine. MS inhibited the 5-HT system more obviously and was relieved by fluoxetine. LPS triggered stronger immune response in the hippocampus and prefrontal cortex (PFC). MS significantly reduced the expression of neurotrophic proteins and was alleviated by fluoxetine. Overall, LPS induced stronger system inflammation, while MS impaired the function of HPA axis and 5-HT system. Our results will contribute to a deeper understanding of the pathophysiology of different stress-induced depression and will also help researchers select appropriate models of depression for their own needs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12888-022-04233-2. BioMed Central 2022-09-05 /pmc/articles/PMC9443001/ /pubmed/36064335 http://dx.doi.org/10.1186/s12888-022-04233-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yu, Xiaojin
Yao, Hui
Zhang, Xiaohui
Liu, Lulu
Liu, Shuangmei
Dong, Youjing
Comparison of LPS and MS-induced depressive mouse model: behavior, inflammation and biochemical changes
title Comparison of LPS and MS-induced depressive mouse model: behavior, inflammation and biochemical changes
title_full Comparison of LPS and MS-induced depressive mouse model: behavior, inflammation and biochemical changes
title_fullStr Comparison of LPS and MS-induced depressive mouse model: behavior, inflammation and biochemical changes
title_full_unstemmed Comparison of LPS and MS-induced depressive mouse model: behavior, inflammation and biochemical changes
title_short Comparison of LPS and MS-induced depressive mouse model: behavior, inflammation and biochemical changes
title_sort comparison of lps and ms-induced depressive mouse model: behavior, inflammation and biochemical changes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443001/
https://www.ncbi.nlm.nih.gov/pubmed/36064335
http://dx.doi.org/10.1186/s12888-022-04233-2
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