{"title":"红核IL-15通过诱导炎症因子促进雄性大鼠神经性疼痛的发生,提示NF-κB和p38 MAPK的参与。","authors":"Miao-Miao Zhang, Wen-Tao Wang, Yue-Jia Li, Xiao-Xia Tao, Ke Li, Jia-Min Chen, Qing-Qing Yang, Xue Tian, Jian Yang, Yan-Li Yu, Ya-Li Xu, Ji-Bo Wu, Jun-Yang Wang, Xiao-Yan Zeng","doi":"10.1016/j.bbi.2025.106137","DOIUrl":null,"url":null,"abstract":"<p><p>Our recent studies have identified that the red nucleus (RN), a prominent motor regulatory nucleus situated in the midbrain tegmentum, is involved in the development of neuropathic pain. However, the molecular mechanisms by which the RN mediates pain regulation are still far from clear. Here, we report that the RN modulates neuropathic pain through secreting IL-15, a member of the immunomodulatory cytokine family. Following spared nerve injury (SNI) of male rats, IL-15 and its receptor IL-15Rα were boosted in the RN, especially within neurons and microglia, during the development stage of neuropathic pain. Knockdown of red nucleus IL-15 alleviated SNI-induced neuropathic pain, whereas intrarubral administration of exogenous IL-15 evoked abnormal pain in naive rats. Further studies indicated that red nucleus IL-15 exerted algesic effect by inducing the production of inflammatory factors, including cytokines TNF-α and IL-1β, chemokine CXCL11, and complement component C4a. Blockade of these inflammatory factors alleviated IL-15-mediated neuropathic pain. Additionally, our data demonstrated that NF-κB and p38 MAPK signaling pathways were involved in red nucleus IL-15-mediated neuropathic pain, in which p38 MAPK pathway contributed to IL-15-induced release of TNF-α and IL-1β, while both NF-κB and p38 MAPK pathways contributed to IL-15-induced secretion of CXCL11 and C4a. Inhibition of red nucleus NF-κB or p38 MAPK suppressed the upregulation of TNF-α, IL-1β, CXCL11 and/or C4a, and alleviated red nucleus IL-15-mediated neuropathic pain. These findings provide mechanistic insights by which red nucleus IL-15 facilitates the development of neuropathic pain and highlight its potential as a therapeutic target for refractory neuropathic pain.</p>","PeriodicalId":9199,"journal":{"name":"Brain, Behavior, and Immunity","volume":" ","pages":"106137"},"PeriodicalIF":7.6000,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Red nucleus IL-15 facilitates the development of neuropathic pain in male rats by inducing inflammatory factors: implying the involvement of NF-κB and p38 MAPK.\",\"authors\":\"Miao-Miao Zhang, Wen-Tao Wang, Yue-Jia Li, Xiao-Xia Tao, Ke Li, Jia-Min Chen, Qing-Qing Yang, Xue Tian, Jian Yang, Yan-Li Yu, Ya-Li Xu, Ji-Bo Wu, Jun-Yang Wang, Xiao-Yan Zeng\",\"doi\":\"10.1016/j.bbi.2025.106137\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Our recent studies have identified that the red nucleus (RN), a prominent motor regulatory nucleus situated in the midbrain tegmentum, is involved in the development of neuropathic pain. However, the molecular mechanisms by which the RN mediates pain regulation are still far from clear. Here, we report that the RN modulates neuropathic pain through secreting IL-15, a member of the immunomodulatory cytokine family. Following spared nerve injury (SNI) of male rats, IL-15 and its receptor IL-15Rα were boosted in the RN, especially within neurons and microglia, during the development stage of neuropathic pain. Knockdown of red nucleus IL-15 alleviated SNI-induced neuropathic pain, whereas intrarubral administration of exogenous IL-15 evoked abnormal pain in naive rats. Further studies indicated that red nucleus IL-15 exerted algesic effect by inducing the production of inflammatory factors, including cytokines TNF-α and IL-1β, chemokine CXCL11, and complement component C4a. Blockade of these inflammatory factors alleviated IL-15-mediated neuropathic pain. Additionally, our data demonstrated that NF-κB and p38 MAPK signaling pathways were involved in red nucleus IL-15-mediated neuropathic pain, in which p38 MAPK pathway contributed to IL-15-induced release of TNF-α and IL-1β, while both NF-κB and p38 MAPK pathways contributed to IL-15-induced secretion of CXCL11 and C4a. Inhibition of red nucleus NF-κB or p38 MAPK suppressed the upregulation of TNF-α, IL-1β, CXCL11 and/or C4a, and alleviated red nucleus IL-15-mediated neuropathic pain. These findings provide mechanistic insights by which red nucleus IL-15 facilitates the development of neuropathic pain and highlight its potential as a therapeutic target for refractory neuropathic pain.</p>\",\"PeriodicalId\":9199,\"journal\":{\"name\":\"Brain, Behavior, and Immunity\",\"volume\":\" \",\"pages\":\"106137\"},\"PeriodicalIF\":7.6000,\"publicationDate\":\"2025-10-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain, Behavior, and Immunity\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.bbi.2025.106137\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain, Behavior, and Immunity","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.bbi.2025.106137","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
Red nucleus IL-15 facilitates the development of neuropathic pain in male rats by inducing inflammatory factors: implying the involvement of NF-κB and p38 MAPK.
Our recent studies have identified that the red nucleus (RN), a prominent motor regulatory nucleus situated in the midbrain tegmentum, is involved in the development of neuropathic pain. However, the molecular mechanisms by which the RN mediates pain regulation are still far from clear. Here, we report that the RN modulates neuropathic pain through secreting IL-15, a member of the immunomodulatory cytokine family. Following spared nerve injury (SNI) of male rats, IL-15 and its receptor IL-15Rα were boosted in the RN, especially within neurons and microglia, during the development stage of neuropathic pain. Knockdown of red nucleus IL-15 alleviated SNI-induced neuropathic pain, whereas intrarubral administration of exogenous IL-15 evoked abnormal pain in naive rats. Further studies indicated that red nucleus IL-15 exerted algesic effect by inducing the production of inflammatory factors, including cytokines TNF-α and IL-1β, chemokine CXCL11, and complement component C4a. Blockade of these inflammatory factors alleviated IL-15-mediated neuropathic pain. Additionally, our data demonstrated that NF-κB and p38 MAPK signaling pathways were involved in red nucleus IL-15-mediated neuropathic pain, in which p38 MAPK pathway contributed to IL-15-induced release of TNF-α and IL-1β, while both NF-κB and p38 MAPK pathways contributed to IL-15-induced secretion of CXCL11 and C4a. Inhibition of red nucleus NF-κB or p38 MAPK suppressed the upregulation of TNF-α, IL-1β, CXCL11 and/or C4a, and alleviated red nucleus IL-15-mediated neuropathic pain. These findings provide mechanistic insights by which red nucleus IL-15 facilitates the development of neuropathic pain and highlight its potential as a therapeutic target for refractory neuropathic pain.
期刊介绍:
Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals.
As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.