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北京中医药大学针灸推拿学院,北京 100029
孙丽丽,北京中医药大学硕士研究生。E-mail:18655881329@163.com
✉朱翔宇,副教授。E-mail:116491992@qq.com
收稿:2025-05-13,
网络首发:2026-07-30,
纸质出版:2026-09-12
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孙丽丽, 朱翔宇, 高海南, 等. 从生物力学角度探讨针刀干预膝关节骨关节炎兔膝关节软骨退化的作用机制[J]. 中国针灸, 2026,46(9):1497-1503.
SUN Lili, ZHU Xiangyu, GAO Hainan, et al. Biomechanical effect of acupotomy on cartilage degeneration in rabbits with knee osteoarthritis[J]. Chinese Acupuncture & Moxibustion, 2026, 46(9): 1497-1503.
孙丽丽, 朱翔宇, 高海南, 等. 从生物力学角度探讨针刀干预膝关节骨关节炎兔膝关节软骨退化的作用机制[J]. 中国针灸, 2026,46(9):1497-1503. DOI: 10.13703/j.0255-2930.20250513-k0005.
SUN Lili, ZHU Xiangyu, GAO Hainan, et al. Biomechanical effect of acupotomy on cartilage degeneration in rabbits with knee osteoarthritis[J]. Chinese Acupuncture & Moxibustion, 2026, 46(9): 1497-1503. DOI: 10.13703/j.0255-2930.20250513-k0005.
目的:
2
观察针刀对膝关节骨关节炎(KOA)兔膝关节生物力学特性及软骨退化的影响,探讨针刀治疗KOA的作用机制。
方法:
2
将24只6月龄新西兰雄兔随机分为空白组、模型组和针刀组,每组8只。除空白组外,其余组均采用改良Videman法左后肢伸直位固定制动6周,制备KOA兔模型。针刀组于左后肢膝关节股内侧肌肌腱止点、股外侧肌肌腱止点、股直肌肌腱止点、股二头肌肌腱止点及鹅足腱囊行针刀干预,每周1次,共3周。干预前后,观察兔左后肢膝关节奎森功能障碍指数(Lequesne MG)评分和被动活动度(PROM)。干预结束后,检测兔左后肢膝关节屈伸肌群表面肌电信号均方根振幅(RMS),采集兔起跳瞬间左后肢膝关节作用力,免疫荧光染色法检测兔左后肢膝关节软骨Ⅱ型胶原蛋白(Col-Ⅱ)荧光强度,ELISA法检测兔血清软骨寡聚基质蛋白(COMP)和Ⅱ型胶原羧基端肽(CTX-Ⅱ)含量。
结果:
2
干预后,与空白组比较,模型组Lequesne MG评分升高(
P
<
0.05);PROM降低(
P
<
0.05);左后肢膝关节屈肌肌群和伸肌肌群RMS降低(
P
<
0.05);左后肢膝关节作用力降低(
P
<
0.05);左后肢膝关节软骨Col-Ⅱ荧光强度降低(
P
<
0.05);血清COMP、CTX-Ⅱ含量均升高(
P
<
0.05)。干预后,与模型组比较,针刀组Lequesne MG评分降低(
P
<
0.05);PROM升高(
P
<
0.05);左后肢膝关节屈肌肌群和伸肌肌群RMS升高(
P
<
0.05);左后肢膝关节作用力升高(
P
<
0.05);左后肢膝关节软骨Col-Ⅱ荧光强度升高(
P
<
0.05);血清COMP、CTX-Ⅱ含量均降低(
P
<
0.05)。
结论:
2
针刀干预通过调节膝关节屈伸肌群的激活程度恢复膝关节作用力,抑制细胞外基质降解,进而延缓KOA软骨退化。
Objective
2
To observe the effects of acupotomy on the biomechanical characteristics and cartilage degeneration of knee joint in rabbits with knee osteoarthritis (KOA)
and to explore the therapeutic mechanism of acupotomy in treatment of KOA.
Methods
2
Twenty-four 6-month-old male New Zealand rabbits were randomly assigned to a normal group
a model group and an acupotomy group
8 rabbits in each group. Except the normal group
all other groups underwent the modified Videman method to induce KOA by immobilizing the left hind limb in extension for 6 weeks. In the acupotomy group
acupotomy was operated at the left knee on the tendon insertions of the vastus medialis
vastus lateralis
rectus femoris
and biceps femoris
and on the pes anserine bursa
once a week for 3 weeks. Before and after intervention
the score of Lequesne MG and passive range of motion (PROM) were observed in the knee joint of the rabbit′s left hind limb. After intervention completion
the root mean square (RMS) of surface electromyographic signals from the flexor and extensor muscle groups of the knee joint of the rabbit′s left hind limb was evaluated
the knee joint force exerted by the left hind limb at the moment of takeoff was collected. Immunofluorescence staining was used to detect the fluorescence intensity of type Ⅱcollagen (Col-Ⅱ) in the knee cartilage of rabbit left hind limb
while ELISA was employed to determine the levels of cartilage oligomeric matrix protein (COMP) and type Ⅱ collagen carboxyl-terminal peptide (CTX-Ⅱ) in rabbit serum.
Results
2
After intervention
compared with the normal group
the model group showed the increase in the Lequesne MG score (
P
<
0.05)
and the decrease in PROM
RMS of the flexor and extensor muscle groups
knee joint force of the left hind limb
fluorescence intensi
ty of Col-Ⅱ in the cartilage of the knee joint of the left hind limb (
P
<
0.05)
and the elevation in serum COMP and CTX-Ⅱ(
P
<
0.05). When compared with the model group
the acupotomy group exhibited the decrease in the Lequesne MG score (
P
<
0.05)
and the increase in PROM
RMS in the flexor and extensor muscle groups
knee joint force of the left hind limb
fluorescence intensity of Col-Ⅱ in cartilage of the knee joint of the left hind limb (
P
<
0.05)
and the decline of serum COMP and CTX-Ⅱ(
P
<
0.05).
Conclusion
2
Acupotomy can retard cartilage degeneration in KOA by modulating the activation of flexor and extensor muscle groups of knee joint
strengthening knee joint force
and suppressing extracellular matrix degradation.
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