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
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.
CNS Neurosci Ther. 2025 Mar;31(3):e70360. doi: 10.1111/cns.70360.
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.
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.
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.
Our findings highlighted the therapeutic potential of targeting LC-CA3 projections to mitigate chronic NP and its neuropsychiatric comorbidities via modulation of hippocampal neuroinflammation.
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。
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。
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。
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。