基础医学与临床 ›› 2026, Vol. 46 ›› Issue (8): 1096-1102.doi: 10.16352/j.issn.1001-6325.2026.08.1096

• 研究论文 • 上一篇    下一篇

艾司氯胺酮缓解膝骨关节炎大鼠疼痛

杜金知1, 倪文洋1, 朱荣宇1, 孟治寿2, 杨建新2*   

  1. 1.山西医科大学 麻醉学院,山西 太原 030000;
    2.山西医科大学第二医院 疼痛科,山西 太原 030000
  • 收稿日期:2025-04-03 修回日期:2025-10-12 发布日期:2026-07-22
  • 通讯作者: *yangjxin66@163.com
  • 基金资助:
    山西省中医药管理局科研课题任务(2023ZYYB2024)

Esketamine alleviates pain in rats with knee osteoarthritis

DU Jinzhi1, NI Wenyang1, ZHU Rongyu1, MENG Zhishou2, YANG Jianxin2*   

  1. 1. College of Anesthesiology, Shanxi Medical University, Taiyuan 030000;
    2. Department of Pain, the Second Hospital of Shanxi Medical University, Taiyuan 030000, China
  • Received:2025-04-03 Revised:2025-10-12 Published:2026-07-22
  • Contact: *yangjxin66@163.com

摘要: 目的 探讨艾司氯胺酮(S-KET)调节TLR4/TNF-α/MMP-9信号通路对膝骨关节炎(KOA)大鼠疼痛的影响。方法 采用关节内注入木瓜蛋白酶法构建KOA大鼠模型,并将建模成功的大鼠按照随机数字表法分为KOA组、L-S-KET、M-S-KET、H-S-KET(腹腔注射10、20、40 mg/kg的S-KET)、H-S-KET+LPS组(腹腔注射40 mg/kg的S-KET+关节内注射0.25 mg/kg的TLR4激活剂LPS),每组各10只。另取10只正常大鼠为对照(Control)组,对照组与KOA组给予等量生理盐水,1次/d,连续28 d。热辐射法与痛阈测量仪检测大鼠疼痛阈值;HE染色观察大鼠软骨组织病理变化并进行病理学评分;TUNEL染色观察大鼠软骨组织细胞凋亡情况;ELISA检测大鼠血清IL-6、TNF-α、IL-1β水平;Western blot检测大鼠关节组织中TLR4/TNF-α/MMP-9信号通路蛋白表达。结果 与对照组相比,KOA组大鼠软骨组织失去正常结构,Mankin评分升高(P<0.05);与KOA组相比,L-S-KET组、M-S-KET组、H-S-KET组大鼠软骨受损程度减轻,细胞排列相对均匀,Mankin评分降低(P<0.05);与H-S-KET组相比,H-S-KET+LPS组大鼠软骨组织有裂隙,细胞排列不均匀,Mankin评分升高(P<0.05)。与对照组相比,KOA组大鼠热痛阈值(PWTL)、机械痛阈值(PWMT)降低,软骨组织细胞凋亡率、IL-6、TNF-α、IL-1β水平及TLR4、TNF-α、MMP-9蛋白表达升高(P<0.05)。与KOA组相比,L-S-KET组、M-S-KET组、H-S-KET组大鼠PWTL、PWMT升高,大鼠软骨组织细胞凋亡率、IL-6、TNF-α、IL-1β水平及TLR4、TNF-α、MMP-9蛋白表达降低(P<0.05)。与H-S-KET组相比,H-S-KET+LPS组大鼠PWTL、PWMT降低,大鼠软骨组织细胞凋亡率、IL-6、TNF-α、IL-1β水平及TLR4、TNF-α、MMP-9蛋白表达升高(P<0.05)。结论 S-KET可降低炎性因子水平,缓解大鼠KOA疼痛,这可能是通过调节TLR4/TNF-α/MMP-9信号通路实现的。

关键词: 艾司氯胺酮(S-KET), Toll样受体4(TLR4), 肿瘤坏死因子-α(TNF-α), 基质金属蛋白酶-9(MMP-9), 膝骨关节炎(KOA)

Abstract: Objective To investigate the effect of esketamine (S-KET) on pain in knee osteoarthritis (KOA) rats by modulating the TLR4/TNF-α/MMP-9 signaling pathway. Methods A KOA rat model was established by intra-articular injection of papain. Successfully modeled rats were assigned into KOA group, L-S-KET, M-S-KET, H-S- KET groups (intraperitoneal injection of 10, 20, and 40 mg/kg S-KET), and H-S-KET+LPS group (intraperitoneal injection of 40 mg/kg S-KET+intra-articular injection of 0.25 mg/kg TLR4 activator LPS) according to the random number table method, with 10 rats in each group. Another 10 normal rats served as control group. The control group and KOA group were given equal amounts of physiological saline once a day for 28 consecutive days. The thermal radiation method and pain threshold measurement instrument were used to detect the pain threshold of rats. HE staining was used to observe pathological changes in rat cartilage tissue, and the pathological scoring was performed. TUNEL staining was used to observe the apoptosis of chondrocytes in cartilage tissue. ELISA was performed to detect IL-6, TNF-α, and IL-1β in serum. Western blot was performed to detect changes in the expression of TLR4/TNF-α/MMP-9 signaling pathway proteins in joint tissues. Results Compared with the control group, the cartilage tissue of rats in KOA group lost normal structure and the Mankin score increased (P<0.05). Compared with KOA group, the L-S-KET group, M-S-KET group, and H-S-KET group showed reduced cartilage damage, relatively uniform cell arrangement, and decreased Mankin score(P<0.05). Compared with the H-S-KET group, the H-S-KET+LPS group showed cracks in the cartilage tissue of rats, uneven cell arrangement, and an increase in Mankin score (P<0.05). Compared with the control group, the KOA group had lower thermal pain threshold and mechanical pain threshold, higher chondrocyte apoptosis rate, IL-6, TNF-α, IL-1β levels, and TLR4, TNF-α, MMP-9 protein expression (P<0.05). Compared with the KOA group, the L-S-KET group, M-S-KET group, and H-S-KET group had higher thermal pain threshold and mechanical pain threshold, lower chondrocyte apoptosis rate, IL-6, TNF-α, IL-1β levels, and TLR4, TNF-α, MMP-9 protein expression(P<0.05). Compared with the H-S-KET group, the H-S-KET+LPS group had lower thermal pain threshold and mechanical pain threshold, higher chondrocyte apoptosis rate, IL-6, TNF-α, IL-1β levels, and TLR4, TNF-α, MMP-9 protein expression(P<0.05). Conclusions S-KET can reduce inflammatory factors and alleviate KOA pain in rats. This may be achieved by modulating the TLR4/TNF-α/MMP-9 signaling pathway.

Key words: esketamine(S-KET), toll-like receptor 4(TLR4), tumor necrosis factor-α(TNF-α), matrix metalloproteinase-9(MMP-9), knee osteoarthritis(KOA)

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