首页|期刊导航|福建中医药|基于Fas信号通路探讨荣筋拈痛方改善骨关节炎软骨退变的作用机制

基于Fas信号通路探讨荣筋拈痛方改善骨关节炎软骨退变的作用机制OA

Mechanism of Rongjin Niantong Formula in Improving Cartilage Degeneration in Osteoarthritis Based on Fas Signaling Pathway

中文摘要英文摘要

目的 基于Fas信号通路探讨荣筋拈痛方改善骨关节炎(OA)软骨退变的作用机制.方法 将24只SD雄性大鼠分为对照组8只和造模组16只.造模组采用改良Hulth法建立OA大鼠模型,对照组在右膝关节内侧皮肤切开1 cm,完成切开即缝合.将造模成功的大鼠随机分为模型组和荣筋拈痛方组各8只,荣筋拈痛方组按4.6 g/(kg·d)给予荣筋拈痛方药液灌胃,对照组和模型组按体质量4 mL/(kg·d)给予0.9%生理盐水灌胃.每日灌胃1次,均连续灌胃12周.实验期间观察3组大鼠外观和日常行为,每周在固定时间测量3组大鼠体质量.检测3组血清丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、总胆红素(TBIL)、总蛋白(TP)、球蛋白(GLB)、肌酐(Cr)、尿素氮(BUN)和尿酸(UA)含量;HE染色观察软骨组织病理形态学变化;Western blot检测软骨组织Fas、Fas相关死亡结构域蛋白(FADD)、p-FADD、p53蛋白表达量.结果 实验期间大鼠整体生理状态良好,进食及进水正常,行为活动未见异常改变.HE染色观察发现,对照组软骨结构完整;模型组软骨各层结构破坏明显;荣筋拈痛方组软骨层次相对清晰.3组相同干预时间体质量以及干预后血清ALT、AST、TBIL、TP、GLB、Cr、BUN和UA含量比较,差异均无统计学意义(P>0.05).与对照组比较,模型组软骨组织Fas、p53、FADD蛋白表达量均明显升高(P<0.05),p-FADD蛋白表达量和p-FADD/FADD均明显降低(P<0.05);与模型组比较,荣筋拈痛方组Fas、p53、FADD蛋白表达量均明显降低(P<0.05),p-FADD蛋白表达量和p-FADD/FADD均明显升高(P<0.05).结论 荣筋拈痛方可通过调节Fas信号通路抑制软骨细胞凋亡,改善OA大鼠软骨退变.

Objective:To investigate the mechanism of Rongjin Niantong formula in improving cartilage degeneration in osteo-arthritis(OA)based on the Fas signaling pathway.Methods:Twenty-four male SD rats were divided into a control group of 8 rats and a modeling group of 16 rats.The OA rat model was established using the modified Hulth method in the modeling group,while a 1 cm incision was made on the skin of the medial side of the right knee joint in the control group,which was sutured immediately after incision.The successfully modeled rats were randomly divided into model group and Rongjin Niantong formula group,with 8 rats in each group.The Rongjin Niantong formula group was administered with Rongjin Niantong formula solution by gavage at a dosage of 4.6 g/(kg·d),while the control and model groups were administered with physiological saline by gavage at a dosage of 4 mL/(kg·d).Gavage was performed once daily,and the treatment was continued for 12 consecutive weeks.The appearance and daily behavior of the three groups of rats were observed,and their body weight was measured at a fixed time each week during the experi-mental period.The serum levels of alanine aminotransferase(ALT),aspartate aminotransferase(AST),total bilirubin(TBIL),total protein(TP),globulin(GLB),creatinine(CR),blood urea nitrogen(BUN),and uric acid(UA)were measured in three groups.HE staining was used to observe the pathological morphological changes of cartilage tissue.Western blot was used to detect the protein expressions of Fas,Fas-associated death domain protein(FADD),p-FADD and p53 in cartilage tissue.Results:The overall physio-logical state of the rats was good,with normal food and water intake,and no abnormal changes in behavioral activities were observed during the experimental period.HE staining revealed that the cartilage structure in the control group was intact;the structure of each layer of cartilage in the model group was significantly damaged,while the layers of cartilage in the Rongjin Niantong formula group were relatively clear.There were no statistically significant differences in body weight and post-intervention serum levels of ALT,AST,TBIL,TP,GLB,CR,BUN,and UA among the three groups with the same intervention duration(P>0.05).Compared with the control group,the protein expressions of Fas,p53,and FADD in the cartilage tissue of the model group significantly increased(P<0.05),while the protein expression of p-FADD and the ratio of p-FADD/FADD significantly decreased(P<0.05).Compared with the model group,the protein expressions of Fas,p53,and FADD in the Rongjin Niantong formula group significantly decreased(P<0.05),while the protein expression of p-FADD and the ratio of p-FADD/FADD significantly increased(P<0.05).Conclusion:Rongjin Niantong Formula can inhibit chondrocyte apoptosis and improve cartilage degeneration in OA rats by regulating the Fas sig-naling pathway.

涂斯婉;李家乐;孙少华;段辛威;勾伟颖;王丽丽

福建中医药大学中西医结合学院 中西医结合研究院,福建 福州 350122福建中医药大学中西医结合学院 中西医结合研究院,福建 福州 350122福建中医药大学中西医结合学院 中西医结合研究院,福建 福州 350122福建中医药大学中西医结合学院 中西医结合研究院,福建 福州 350122福建中医药大学中西医结合学院 中西医结合研究院,福建 福州 350122福建中医药大学中西医结合学院 中西医结合研究院,福建 福州 350122||福建省中西医结合老年性疾病重点实验室,福建 福州 350122

骨关节炎荣筋拈痛方软骨退变细胞凋亡Fas信号通路

osteoarthritisRongjin Niantong formulacartilage degenerationapoptosisFas signaling pathway

《福建中医药》 2026 (3)

35-39,5

国家自然科学基金青年科学基金项目(82305267)福建省自然科学基金项目(2022J01371)

10.13260/j.cnki.jfjtcm.2026.03007

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