Yu Wen-Ying, Xiu Zhong-Biao, Lin Ze-Hao, Liu Hong, Zhang Liang-Zhi, Li Yu-Lin, Feng Xiang-Long, Liu Jing
The First Clinical College of Fujian University of Traditional Chinese Medicine, Fuzhou 350122, China.
The Affiliated People's Hospital of Fujian University of Traditional Chinese Medicine, Fuzhou 350004.
Zhen Ci Yan Jiu. 2025 Jun 25;50(6):649-657. doi: 10.13702/j.1000-0607.20240962.
To observe the effects of acupotomy therapy on synovial inflammation, macrophage polarization, and protein expressions of drosophila double-wing edge notch homologous gene 1 (Notch1)/Jagged typical Notch ligand 1 (Jagged1)/Hes family BHLH transcription factor 1 (Hes1) signaling pathway, so as to explore its mechanisms underlying improvement of knee osteoarthritis (KOA).
Male New Zealand rabbits were randomly divided into the blank, model and acupotomy groups (8 rabbits in each group). The KOA model was established by immobilizing the left hind limb in an extended position using a modified Videman method with a plaster cast for 6 weeks. After modeling, 3 meridian lesion points with significant reactions were selected from "Hedingci", "Binwaishang" "Binneishang" "Chengfeijian" "Weiyangci" and "Yinlingci" for acupotomy treatment, once a week for a total of 4 times. X-ray detection was performed after modeling. Behavioral changes in the affected knee joint of the rabbits were observed before and after the intervention and the Lequesne MG scores were recorded. Histopathological changes in the synovial tissue of the left knee joint of rabbits were observed and pathological scores were recorded after HE staining. The positive expressions of cluster differentiation 86 (CD86) and macrophage mannose receptor-1 (CD206) in the synovial tissue were detected by immunohistochemical staining. The mRNA expression levels of inducible nitric oxide synthase (iNOS), CD206, Jagged1, Notch1, arginase-1 (Arg-1) and Hes1 in the synovial tissue were detected by real-time qPCR, and the protein expression levels of Jagged1, Notch1, Arg-1, and Hes1 were detected by Western blot.
Compared with the blank group, the knee joint space of rabbits in the modeling group was significantly narrowed. Compared to the blank group, the model group showed significant increase in Lequesne MG scores (<0.01), pathological scores (<0.01), the positive expressions of CD86 and the mRNA expression levels of iNOS (<0.01), the mRNA and protein expression levels of Notch1, Jagged1 and Hes1 (<0.01, <0.05) in synovial tissue;and a decrease in the positive expression of CD206 (<0.01), the expression levels of CD206 mRNA, and Arg-1 mRNA and protein (<0.01, <0.05). After acupotomy intervention, modeling induced increase and decrease indexes mentioned above were reversed (<0.01, <0.05).
Acupotomy can reduce the inflammatory response in synovial tissue of KOA rabbits by regulating the Notch1/Jagged1/Hes1 signaling pathway and promoting the polarization shift of synovial macrophages from M1-type to M2-type. This may be one of the mechanisms by which acupotomy treats KOA.
观察针刀疗法对滑膜炎症、巨噬细胞极化以及果蝇双翅边缘缺刻同源基因1(Notch1)/锯齿状典型Notch配体1(Jagged1)/Hes家族BHLH转录因子1(Hes1)信号通路蛋白表达的影响,以探讨其改善膝骨关节炎(KOA)的作用机制。
将雄性新西兰兔随机分为空白组、模型组和针刀组(每组8只)。采用改良的Videman法,用石膏固定左后肢于伸直位6周,建立KOA模型。造模后,从“鹤顶刺”“膑外上”“膑内上”“承飞健”“委阳刺”“阴陵刺”中选取3个有明显反应的经络病变点进行针刀治疗,每周1次,共4次。造模后进行X线检测。观察干预前后兔患侧膝关节的行为变化并记录Lequesne MG评分。观察兔左膝关节滑膜组织的组织病理学变化,HE染色后记录病理评分。采用免疫组织化学染色检测滑膜组织中分化簇86(CD86)和巨噬细胞甘露糖受体-1(CD206)的阳性表达。采用实时荧光定量PCR检测滑膜组织中诱导型一氧化氮合酶(iNOS)、CD206、Jagged1、Notch1、精氨酸酶-1(Arg-1)和Hes1的mRNA表达水平,采用蛋白质印迹法检测Jagged1、Notch1、Arg-1和Hes1的蛋白表达水平。
与空白组相比,模型组兔膝关节间隙明显变窄。与空白组相比,模型组Lequesne MG评分(<0.01)、病理评分(<0.01)、CD86阳性表达及滑膜组织中iNOS的mRNA表达水平(<0.01)、Notch1、Jagged1和Hes1的mRNA及蛋白表达水平(<0.01,<0.05)均显著升高;CD206阳性表达(<0.01)、CD206 mRNA表达水平以及Arg-1 mRNA和蛋白表达水平(<0.01,<0.05)降低。针刀干预后,上述造模诱导的升高和降低指标均得到逆转(<0.01,<0.05)。
针刀可通过调节Notch1/Jagged1/Hes1信号通路,促进KOA兔滑膜巨噬细胞从M1型向M2型极化转变,从而减轻滑膜组织的炎症反应。这可能是针刀治疗KOA的机制之一。