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右美托咪定通过抑制TLR-4/NF-κB通路改善压力应激小鼠的乳腺肿瘤治疗效果

张楚逸 孟珊 徐鑫 范鹏 冒讯圆 黄玉辉 靳三庆

中山大学学报(医学科学版)2026,Vol.47Issue(4):601-612,12.
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中山大学学报(医学科学版)2026,Vol.47Issue(4):601-612,12.DOI:10.11714/jsysu.med.YX20260018

右美托咪定通过抑制TLR-4/NF-κB通路改善压力应激小鼠的乳腺肿瘤治疗效果

Dexmedetomidine Improves the Therapeutic Efficacy Against Mammary Tumors in Stress-exposed Mice by Inhibiting the TLR4/NF-κB Pathway

张楚逸 1孟珊 1徐鑫 2范鹏 2冒讯圆 2黄玉辉 2靳三庆1

作者信息

  • 1. 中山大学附属第六医院麻醉科,广东 广州 510655||广州市黄埔区中六生物医学创新研究院,广东 广州 510005
  • 2. 苏州大学唐仲英血液学研究中心,江苏 苏州 215123
  • 折叠

摘要

Abstract

[Objective]This study aimed to investigate whether dexmedetomidine(Dex)alleviates stress-induced mammary tumor progression in mice by inhibiting the TLR4/NF-κB signaling pathway,and to examine its effects on anxiety-depression-like behaviors and stress hormone levels.[Methods]An orthotopic EMT6 mammary tumor model was established in mice,and chronic mild stress(CMS)was applied to induce anxiety-depression-like states.The mice were divided into six groups:naive,tumor,CMS,CMS+tumor,CMS+tumor+Dex,and CMS+tumor+Vehicle groups.Behavioral changes were evaluated using the open field test and tail suspension test.Plasma stress hormone levels were measured by high-performance liquid chromatography.Western blot and RT-qPCR were performed to detect the expression of TLR4,p-NF-κB p65,p-IκBα,and inflammatory cytokines(IL-6,IL-1β,TNF-α)in tumor tissues.In vitro,EMT6 cells were treated with cortisol to mimic the stress-related microenvironment,and the effects of Dex on the TLR4/NF-κB pathway were assessed by CCK-8,Western blot,and RT-qPCR.[Results]Tumor-bearing mice exhibited significant anxiety-depression-like behaviors(P<0.05),along with markedly elevated plasma levels of norepinephrine,epinephrine,and cortisol(P<0.05).Chronic stress further aggravated these behavioral abnormalities and promoted tumor growth(P<0.05).Dexmedetomidine intervention significantly improved anxiety-depression-like behaviors(P<0.05)and lowered peripheral stress hormone levels(P<0.05)in stress-exposed tumor-bearing mice.In vitro experiments demonstrated that cortisol treatment activated the TLR4/NF-κB pathway(P<0.001)and upregulated the expression of inflammatory cytokines(P<0.05 in EMT6 cells,whereas dexmedetomidine effectively suppressed this activation(P<0.001).In the in vivo model,dexmedetomidine treatment downregulated the expression of TLR4,p-NF-κB p65,p-IκBα,and pro-inflammatory cytokines in tumor tissues(P<0.001)and significantly inhibited tumor growth(P<0.05).[Conclusion]Dexmedetomidine inhibits the TLR4/NF-κB signaling pathway,alleviates stress-induced inflammatory responses,improves anxiety-and depression-like behaviors,reduces stress hormone levels,and suppresses mammary tumor progression.These findings provide an experimental basis for understanding anxiety-and depression-associated breast tumor progression and suggest that Dexmedetomidine and the TLR4/NF-κB pathway may serve as potential therapeutic targets.

关键词

右美托咪定/TLR4/NF-κB通路/应激/乳腺肿瘤/焦虑-抑郁样行为

Key words

dexmedetomidine/TLR4/NF-κB pathway/stress/mammary tumor/anxiety-and depression-like behavior

分类

医药卫生

引用本文复制引用

张楚逸,孟珊,徐鑫,范鹏,冒讯圆,黄玉辉,靳三庆..右美托咪定通过抑制TLR-4/NF-κB通路改善压力应激小鼠的乳腺肿瘤治疗效果[J].中山大学学报(医学科学版),2026,47(4):601-612,12.

基金项目

国家自然科学基金(82473305) (82473305)

中山大学学报(医学科学版)

1672-3554

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