医学
巨噬细胞极化
背根神经节
痛觉过敏
肿瘤坏死因子α
炎症
促炎细胞因子
M2巨噬细胞
内分泌学
弗氏佐剂
巨噬细胞
内科学
脊髓
下调和上调
小胶质细胞
药理学
免疫学
伤害
受体
化学
生物化学
体外
精神科
基因
作者
Md. Mahbubur Rahman,Sung-Min Hwang,Eun Jin Go,Yong Ho Kim,Chul‐Kyu Park
标识
DOI:10.1016/j.biopha.2024.117157
摘要
Although the potent anti-inflammatory effects of irisin have been documented in various inflammatory disorders, its efficacy against inflammatory pain remains unexplored. Herein, we examined the therapeutic effects of irisin in a mouse model of inflammatory pain induced by complete Freund's adjuvant (CFA). Mice were divided into three groups: normal control, CFA-injected (CFA), and CFA plus irisin-treated (CFA+Irisin). The irisin-treated group exhibited a gradual reduction in mechanical allodynia and thermal hyperalgesia when compared with the CFA group. Moreover, treatment with irisin significantly upregulated the expression of M2 macrophage markers (interleukin [IL]-4 and IL-10) and downregulated M1 macrophage markers (IL-1β, IL-6, and tumor necrosis factor-α) in the local paw tissue, dorsal root ganglion, and spinal cord tissue. However, there was no significant difference in the total number of F4/80
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