• 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

脂多糖和慢性不可预知温和应激诱导抑郁模型鼠的比较:行为、炎症和生化改变。

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

机构信息

Department of Anesthesiology, Shengjing Hospital of China Medical University, No. 36 Sanhao Street, Shenyang, Liaoning, 110004, P. R. China.

Department of Forensic Pathology, School of Forensic Medicine, China Medical University, Shenyang, Liaoning, 110012, P. R. China.

出版信息

BMC Psychiatry. 2022 Sep 5;22(1):590. doi: 10.1186/s12888-022-04233-2.

DOI:10.1186/s12888-022-04233-2
PMID:36064335
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9443001/
Abstract

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.

摘要

抑郁症是一种涉及复杂病理生理机制的精神疾病,有许多方法可以建立抑郁小鼠模型。本研究旨在全面比较两种不同模型引起的行为变化及其机制。本研究通过母体分离(MS)或脂多糖(LPS)给药分别建立了两种抑郁小鼠模型,并分别添加氟西汀治疗组进行比较。MS 诱导出更明显的焦虑样行为,而 LPS 诱导出更明显的抑郁样行为。LPS 增加外周炎症因子更明显,氟西汀减轻了这种作用。MS 更明显地抑制 5-HT 系统,氟西汀缓解了这种作用。LPS 在海马体和前额叶皮层(PFC)中引发更强的免疫反应。MS 显著降低神经营养蛋白的表达,氟西汀缓解了这一现象。总的来说,LPS 诱导更强的系统炎症,而 MS 损害 HPA 轴和 5-HT 系统的功能。我们的研究结果将有助于更深入地了解不同应激诱导的抑郁症的病理生理学,并将有助于研究人员根据自身需求选择合适的抑郁症模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/64c232ab0c93/12888_2022_4233_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/f2fe23575643/12888_2022_4233_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/cc819c636cb8/12888_2022_4233_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/8f70dce01be4/12888_2022_4233_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/5b7068f3de17/12888_2022_4233_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/6f33f1f18484/12888_2022_4233_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/64c232ab0c93/12888_2022_4233_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/f2fe23575643/12888_2022_4233_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/cc819c636cb8/12888_2022_4233_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/8f70dce01be4/12888_2022_4233_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/5b7068f3de17/12888_2022_4233_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/6f33f1f18484/12888_2022_4233_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c52/9443001/64c232ab0c93/12888_2022_4233_Fig6_HTML.jpg

相似文献

1
Comparison of LPS and MS-induced depressive mouse model: behavior, inflammation and biochemical changes.脂多糖和慢性不可预知温和应激诱导抑郁模型鼠的比较:行为、炎症和生化改变。
BMC Psychiatry. 2022 Sep 5;22(1):590. doi: 10.1186/s12888-022-04233-2.
2
Fluoxetine combined with swimming exercise synergistically reduces lipopolysaccharide-induced depressive-like behavior by normalizing the HPA axis and brain inflammation in mice.氟西汀联合游泳运动通过调节 HPA 轴和脑内炎症发挥协同作用,减轻脂多糖诱导的小鼠抑郁样行为。
Pharmacol Biochem Behav. 2023 Nov;232:173640. doi: 10.1016/j.pbb.2023.173640. Epub 2023 Sep 21.
3
Exercise and fluoxetine treatment during adolescence protect against early life stress-induced behavioral abnormalities in adult rats.青春期锻炼和氟西汀治疗可预防成年大鼠早期生活应激诱导的行为异常。
Pharmacol Biochem Behav. 2021 Jun;205:173190. doi: 10.1016/j.pbb.2021.173190. Epub 2021 Apr 15.
4
Inhibition of JNK ameliorates depressive-like behaviors and reduces the activation of pro-inflammatory cytokines and the phosphorylation of glucocorticoid receptors at serine 246 induced by neuroinflammation.抑制 JNK 可改善抑郁样行为,并减少神经炎症引起的促炎细胞因子的激活和糖皮质激素受体丝氨酸 246 的磷酸化。
Psychoneuroendocrinology. 2020 Mar;113:104580. doi: 10.1016/j.psyneuen.2019.104580. Epub 2019 Dec 27.
5
Chronic activation of NPFFR2 stimulates the stress-related depressive behaviors through HPA axis modulation.NPFFR2的慢性激活通过下丘脑-垂体-肾上腺(HPA)轴调节刺激与应激相关的抑郁行为。
Psychoneuroendocrinology. 2016 Sep;71:73-85. doi: 10.1016/j.psyneuen.2016.05.014. Epub 2016 May 18.
6
Jmjd3 is involved in the susceptibility to depression induced by maternal separation via enhancing the neuroinflammation in the prefrontal cortex and hippocampus of male rats.Jmjd3 通过增强雄性大鼠前额叶皮层和海马体的神经炎症,参与了母体分离诱导的抑郁易感性。
Exp Neurol. 2020 Jun;328:113254. doi: 10.1016/j.expneurol.2020.113254. Epub 2020 Feb 19.
7
Mitochondrial signaling in inflammation-induced depressive behavior in female and male rats: The role of glucocorticoid receptor.线粒体信号在雌性和雄性大鼠炎症诱导的抑郁行为中的作用:糖皮质激素受体的作用。
Brain Res Bull. 2019 Aug;150:317-327. doi: 10.1016/j.brainresbull.2019.06.016. Epub 2019 Jun 25.
8
Male-specific effects of lipopolysaccharide on glucocorticoid receptor nuclear translocation in the prefrontal cortex of depressive rats.脂多糖对抑郁大鼠前额叶皮质糖皮质激素受体核转位的雄性特异性影响。
Psychopharmacology (Berl). 2016 Sep;233(18):3315-30. doi: 10.1007/s00213-016-4374-y. Epub 2016 Jul 7.
9
Atorvastatin prevents lipopolysaccharide-induced depressive-like behaviour in mice.阿托伐他汀可预防脂多糖诱导的小鼠抑郁样行为。
Brain Res Bull. 2019 Mar;146:279-286. doi: 10.1016/j.brainresbull.2019.01.018. Epub 2019 Jan 25.
10
Potential Role of Bmal1 in Lipopolysaccharide-Induced Depression-Like Behavior and its Associated "Inflammatory Storm".Bmal1 在脂多糖诱导的抑郁样行为及其相关“炎症风暴”中的潜在作用
J Neuroimmune Pharmacol. 2024 Feb 2;19(1):4. doi: 10.1007/s11481-024-10103-3.

引用本文的文献

1
Progress in Molecular Mechanisms of Depression Induced by Mother-Infant Separation and Intervention of Traditional Chinese Medicine.母婴分离所致抑郁症的分子机制研究进展及中医药干预
Alpha Psychiatry. 2025 Aug 11;26(4):45684. doi: 10.31083/AP45684. eCollection 2025 Aug.
2
Antidepressant Activity of Agarwood Essential Oil: A Mechanistic Study on Inflammatory and Neuroprotective Signaling Pathways.沉香精油的抗抑郁活性:关于炎症和神经保护信号通路的机制研究
Pharmaceuticals (Basel). 2025 Feb 14;18(2):255. doi: 10.3390/ph18020255.
3
Tofacitinib prevents depressive-like behaviors through decreased hippocampal microgliosis and increased BDNF levels in both LPS-induced and CSDS-induced mice.

本文引用的文献

1
Chronic ethanol exposure induced anxiety-like behaviour by altering gut microbiota and GABA system.慢性乙醇暴露通过改变肠道微生物群和 GABA 系统引起焦虑样行为。
Addict Biol. 2022 Sep;27(5):e13203. doi: 10.1111/adb.13203.
2
Preventive effects of the AMPA receptor potentiator LY450108 in an LPS-induced depressive mouse model.AMPA 受体增强剂 LY450108 在脂多糖诱导的抑郁小鼠模型中的预防作用
Behav Brain Res. 2022 Apr 29;424:113813. doi: 10.1016/j.bbr.2022.113813. Epub 2022 Feb 22.
3
AMPAkine CX516 alleviated chronic ethanol exposure-induced neurodegeneration and depressive-like behavior in mice.
托法替布通过降低脂多糖诱导和慢性社会挫败应激诱导的小鼠海马小胶质细胞增生以及提高脑源性神经营养因子水平来预防抑郁样行为。
Acta Pharmacol Sin. 2025 Feb;46(2):353-365. doi: 10.1038/s41401-024-01384-8. Epub 2024 Sep 30.
4
Exploring the similarities between risk factors triggering depression in humans and elevated in-cage "inactive but awake" behavior in laboratory mice.探索引发人类抑郁症的风险因素与实验室小鼠笼内“不活动但清醒”行为增加之间的相似性。
Front Vet Sci. 2024 Mar 28;11:1348928. doi: 10.3389/fvets.2024.1348928. eCollection 2024.
5
Targeting Large-Conductance Calcium-Activated Potassium Channels to Ameliorate Lipopolysaccharide-Induced Depressive-Like Behavior in Mice.靶向大电导钙激活钾通道改善脂多糖诱导的小鼠抑郁样行为。
Neurochem Res. 2024 May;49(5):1239-1253. doi: 10.1007/s11064-024-04111-1. Epub 2024 Feb 21.
6
Currently Used Methods to Evaluate the Efficacy of Therapeutic Drugs and Kidney Safety.目前用于评估治疗药物疗效和肾脏安全性的方法。
Biomolecules. 2023 Oct 26;13(11):1581. doi: 10.3390/biom13111581.
7
Global research trends on maternal separation paradigms as an early life stress model: A bibliometric analysis.作为早期生活应激模型的母婴分离范式的全球研究趋势:文献计量分析
Heliyon. 2023 Jul 20;9(8):e18469. doi: 10.1016/j.heliyon.2023.e18469. eCollection 2023 Aug.
8
Gut microbiota regulates chronic ethanol exposure-induced depressive-like behavior through hippocampal NLRP3-mediated neuroinflammation.肠道微生物群通过海马 NLRP3 介导体炎性神经炎症调节慢性乙醇暴露诱导的抑郁样行为。
Mol Psychiatry. 2023 Feb;28(2):919-930. doi: 10.1038/s41380-022-01841-y. Epub 2022 Oct 24.
AMPA 受体激动剂 CX516 减轻了慢性乙醇暴露诱导的小鼠神经退行性变和抑郁样行为。
Toxicol Appl Pharmacol. 2022 Mar 15;439:115924. doi: 10.1016/j.taap.2022.115924. Epub 2022 Feb 15.
4
Chronic ethanol exposure induced depressive-like behavior in male C57BL/6 N mice by downregulating GluA1.慢性乙醇暴露通过下调 GluA1 诱导雄性 C57BL/6N 小鼠出现抑郁样行为。
Physiol Behav. 2021 May 15;234:113387. doi: 10.1016/j.physbeh.2021.113387. Epub 2021 Mar 11.
5
Ibrutinib alleviates LPS-induced neuroinflammation and synaptic defects in a mouse model of depression.依鲁替尼可减轻 LPS 诱导的抑郁模型中小鼠的神经炎症和突触缺陷。
Brain Behav Immun. 2021 Feb;92:10-24. doi: 10.1016/j.bbi.2020.11.008. Epub 2020 Nov 10.
6
Chronic ethanol exposure induces neuroinflammation in H4 cells through TLR3 / NF-κB pathway and anxiety-like behavior in male C57BL/6 mice.慢性乙醇暴露通过 TLR3/NF-κB 通路诱导 H4 细胞神经炎症和雄性 C57BL/6 小鼠焦虑样行为。
Toxicology. 2020 Dec 15;446:152625. doi: 10.1016/j.tox.2020.152625. Epub 2020 Nov 5.
7
Effects of Early-Life Stress on the Brain and Behaviors: Implications of Early Maternal Separation in Rodents.早期生活应激对大脑和行为的影响:啮齿动物中早期母婴分离的影响。
Int J Mol Sci. 2020 Sep 29;21(19):7212. doi: 10.3390/ijms21197212.
8
The Bidirectional Relationship of Depression and Inflammation: Double Trouble.抑郁和炎症的双向关系:双重麻烦。
Neuron. 2020 Jul 22;107(2):234-256. doi: 10.1016/j.neuron.2020.06.002. Epub 2020 Jun 17.
9
The microbiota and the hypothalamus-pituitary-adrenocortical (HPA) axis, implications for anxiety and stress disorders.肠道微生物群与下丘脑-垂体-肾上腺皮质轴:与焦虑和应激障碍的关系。
Curr Opin Neurobiol. 2020 Jun;62:76-82. doi: 10.1016/j.conb.2019.12.003. Epub 2020 Jan 20.
10
Epigenetics and depression
.表观遗传学与抑郁症
Dialogues Clin Neurosci. 2019 Dec;21(4):397-405. doi: 10.31887/DCNS.2019.21.4/ebinder.