时间标签:数据日期 2026-11-05 · 生成时间 2026-11-05 05:30(Asia/Shanghai)| 检索窗口 PubMed edat 2026/11/02 – 2026/11/06 | 情报发生日期 2026-11-05
证据级别:摘要级。本条依据 PubMed 结构化摘要与元数据撰写,付费墙全文未获取、未逐节核验,本站未做任何数值推算补全。
摘要(PubMed 原文节选)
Fibromyalgia (FM) is a chronic pain disorder characterized by widespread musculoskeletal pain accompanied by fatigue, mood disturbances, and sleep abnormalities. Baricitinib, a selective Janus kinase (JAK) 1/2 inhibitor, has potent anti-inflammatory and immunomodulatory effects and is approved for various resistant inflammatory conditions…
对本项目的价值
参考价值:属「营养感知—自噬—蛋白稳态轴」方向;mTOR / 自噬 / 蛋白质稳态栏目可用作本项目文献库与综述素材。 | 价值分 1.8/5(★★☆☆☆)
全文不可及原因
无 PMCID 且 Europe PMC / OpenAlex / Unpaywall 未提供可下载 OA 全文
原文题录
- 中文题名:JAK2/STAT3、PI3K/AKT/mTOR 与 M1/M2 小胶质细胞极化参与巴瑞替尼缓解利血平诱导大鼠纤维肌痛的可能机制
- 英文标题:Involvement of JAK2/STAT3, PI3K/AKT/mTOR, and M1/M2 microglial polarization in the possible effects of baricitinib for mitigating reserpine-induced fibromyalgia in rats.
- 期刊与标识:International immunopharmacology · PMID 42971140 · DOI 10.1016/j.intimp.2026.117637