Suppr超能文献

去甲肾上腺素能蓝斑- CA3激活通过抑制SNI小鼠小胶质细胞神经炎症减轻神经性疼痛及焦虑和抑郁样行为。

Noradrenergic Locus Coeruleus-CA3 Activation Alleviates Neuropathic Pain and Anxiety- and Depression-Like Behaviors by Suppressing Microglial Neuroinflammation in SNI Mice.

作者信息

Zou Helin, Pu Weiyu, Zhou Junli, Li Juan, Ma Lulin, Wang Shuxian, Liu Chengxi, Mou Jing, Liu Xingfeng, Yu Tian, Wei Yiyong, Xie Haihui, Cao Song

机构信息

Department of Anesthesiology, the Tenth Affiliated Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, Guangdong, China.

Dongguan Key Laboratory of Anesthesia and Organ Protection, Dongguan, Guangdong, China.

出版信息

CNS Neurosci Ther. 2025 Mar;31(3):e70360. doi: 10.1111/cns.70360.

Abstract

OBJECTIVE

Neuropathic pain (NP) arises from neuroimmune interactions following nerve injury and is often accompanied by anxiety and depression. The aim of the study is to evaluate the effects of the noradrenergic locus coeruleus (LC), a key regulator of pain and emotional states, projects extensively to the hippocampus.

METHOD

We investigated the effects of chronic NP on LC integrity and its projections to the hippocampal CA3 region in spared nerve injury (SNI) mice with behavioral tests, immunohistochemistry, neurochemical analyses, and Gq-DREADD.

RESULTS

Chronic NP induced LC neuronal loss, reduced hippocampal norepinephrine (NE) release, and triggered microglial activation and neuroinflammation in CA3. Selective activation of LC-CA3 noradrenergic neurons using Gq-DREADD chemogenetics alleviated NP and comorbid anxiety- and depression-like behaviors. This intervention suppressed microglial activation, decreased proinflammatory cytokines (TNF-α and IL-1β), and restored NE levels in CA3.

CONCLUSION

Our findings highlighted the therapeutic potential of targeting LC-CA3 projections to mitigate chronic NP and its neuropsychiatric comorbidities via modulation of hippocampal neuroinflammation.

摘要

目的

神经性疼痛(NP)源于神经损伤后的神经免疫相互作用,常伴有焦虑和抑郁。本研究旨在评估去甲肾上腺素能蓝斑核(LC)的作用,LC是疼痛和情绪状态的关键调节因子,广泛投射至海马体。

方法

我们通过行为测试、免疫组织化学、神经化学分析和Gq-DREADD技术,研究慢性NP对 spared nerve injury(SNI)小鼠LC完整性及其向海马CA3区投射的影响。

结果

慢性NP导致LC神经元丢失,海马去甲肾上腺素(NE)释放减少,并引发CA3区小胶质细胞活化和神经炎症。使用Gq-DREADD化学遗传学选择性激活LC-CA3去甲肾上腺素能神经元可减轻NP以及共病的焦虑和抑郁样行为。该干预措施抑制了小胶质细胞活化,降低了促炎细胞因子(TNF-α和IL-1β)水平,并恢复了CA3区的NE水平。

结论

我们的研究结果突出了靶向LC-CA3投射通过调节海马神经炎症来减轻慢性NP及其神经精神共病的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b919/11933858/9ec380bb61b9/CNS-31-e70360-g004.jpg

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