Sun Yanfei, Cao Jing, Xu Chunpeng, Sun Jiangtao, Liu Xiaofeng, Shi Zhenguang, An SiMeng, Zhao Danyang, Sun Dongjie, Wang Xuxin, Zhao Guoyan, Zhang Chi, Li Guangjian, Xiao Jinyu, Yang Jing, Zhao Hua
School of Life Sciences, Changchun Normal University, Changchun, 130021, China.
Department of Physiology, College of Basic Medical Sciences, Jilin University, Changchun, 130021, China.
J Headache Pain. 2025 May 6;26(1):105. doi: 10.1186/s10194-025-02052-w.
The monoamine system, particularly the serotonergic neurons in the dorsal raphe nucleus (DRN), associated with the synthesis and release of 5-hydroxytryptamine, is crucial for regulating pain. The lateral habenula (LHb) modulates DRN neurons by acting through GABAergic neurons located in the rostromedial tegmental nucleus (RMTg). However, the role of RMTg in mediating the LHb and regulating pain remains unclear. Thus, we aimed to assess the role of the LHb-RMTg pathway in inflammatory pain.
Male C57BL/6 mice were used in the chemogenetic experiments, while male and female Vglut2-ires-cre mice were used in the optogenetic experiments; in both experiments, inflammatory pain model and control groups were established. We performed the Hargreaves and Von Frey tests to assess nociceptive behavior as well as immunohistochemistry staining after chemogenetic activation experiments. Statistical analyses were performed using a t-test, one-way analysis of variance (normally distributed data) or Kruskal-Wallis test (non-normally distributed data) and two-way analysis of variance.
Chemogenetic activation/inhibition of RMTg-projecting LHb excitatory neurons was sufficient to decrease or increase heat sensitivity thresholds. Additionally, inhibition of the LHb-RMTg circuit reversed the decreased heat sensitivity thresholds under inflammatory pain conditions using chemogenetic and optogenetic approaches. However, this circuit did not affect mechanical allodynia thresholds, and chemogenetic activation of the circuit decreased c-Fos immunoreactivity in the DRN.
Our results indicate that activating glutamatergic neurons within the LHb heightens pain sensitivity by triggering GABAergic neurons in the RMTg, which in turn influences neuronal activity in the DRN. This research offers fresh perspectives on the pain mechanism, potentially revealing new therapeutic avenues for managing inflammatory pain.
单胺系统,尤其是中缝背核(DRN)中的5-羟色胺能神经元,与5-羟色胺的合成和释放相关,对疼痛调节至关重要。外侧缰核(LHb)通过作用于位于嘴内侧被盖核(RMTg)的GABA能神经元来调节DRN神经元。然而,RMTg在介导LHb和调节疼痛中的作用仍不清楚。因此,我们旨在评估LHb-RMTg通路在炎性疼痛中的作用。
化学遗传学实验使用雄性C57BL/6小鼠,光遗传学实验使用雄性和雌性Vglut2-ires-cre小鼠;在两个实验中均建立炎性疼痛模型和对照组。我们进行了热辐射甩尾试验和von Frey试验以评估伤害性感受行为,并在化学遗传学激活实验后进行免疫组织化学染色。使用t检验、单因素方差分析(正态分布数据)或Kruskal-Wallis检验(非正态分布数据)以及双因素方差分析进行统计分析。
化学遗传学激活/抑制投射到RMTg的LHb兴奋性神经元足以降低或提高热敏感性阈值。此外,使用化学遗传学和光遗传学方法抑制LHb-RMTg回路可逆转炎性疼痛条件下降低的热敏感性阈值。然而,该回路不影响机械性异常性疼痛阈值,并且该回路的化学遗传学激活降低了DRN中的c-Fos免疫反应性。
我们的结果表明,激活LHb内的谷氨酸能神经元通过触发RMTg中的GABA能神经元来提高疼痛敏感性,进而影响DRN中的神经元活动。这项研究为疼痛机制提供了新的视角,可能揭示治疗炎性疼痛的新途径。