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安徽中医药大学针灸推拿学院,合肥 230012
淮北市人民医院中医科,安徽淮北 235099
经脉脏腑相关安徽省重点实验室,合肥 230038
湖北中医药高等专科学校
安徽省中医药科学院针灸经络研究所,合肥 230038
✉吴子建,教授。E-mail:wuzijian@ahtcm.edu.cn
收稿:2025-08-05,
网络首发:2025-11-26,
纸质出版:2026-02-12
移动端阅览
刘磊, 魏霞, 高子瞻, 等. 艾灸“足三里”对KOA模型大鼠膝关节软骨氨基酸代谢的影响[J]. 中国针灸, 2026,46(2):251-260.
LIU Lei, WEI Xia, GAO Zizhan, et al. Effect of moxibustion at "Zusanli" (ST36) on amino acid metabolism of knee cartilage in KOA rats[J]. Chinese Acupuncture & Moxibustion, 2026, 46(2): 251-260.
刘磊, 魏霞, 高子瞻, 等. 艾灸“足三里”对KOA模型大鼠膝关节软骨氨基酸代谢的影响[J]. 中国针灸, 2026,46(2):251-260. DOI: 10.13703/j.0255-2930.20250805-k0004.
LIU Lei, WEI Xia, GAO Zizhan, et al. Effect of moxibustion at "Zusanli" (ST36) on amino acid metabolism of knee cartilage in KOA rats[J]. Chinese Acupuncture & Moxibustion, 2026, 46(2): 251-260. DOI: 10.13703/j.0255-2930.20250805-k0004.
目的:
2
观察艾灸“足三里”对膝关节骨关节炎(KOA)大鼠膝关节软骨氨基酸代谢的影响,探讨艾灸缓解KOA膝关节软骨损伤的机制。
方法:
2
将30只雄性SD大鼠随机分为正常组、模型组与艾灸组,每组10只。模型组与艾灸组大鼠予双侧膝关节腔内注射L-半胱氨酸与木瓜蛋白酶混合液制备KOA模型。艾灸组予艾灸双侧“足三里”,每次30 min,每日1次,连续30 d。造模前后及干预后,测量大鼠膝关节直径;干预后,检测大鼠机械性痛阈值,HE染色法观察大鼠膝关节软骨组织形态,透射电镜观察大鼠膝关节软骨细胞超微结构,ELISA法检测大鼠膝关节滑膜组织基质金属蛋白酶-13(MMP-13)与白细胞介素-1β(IL-1β)含量,液相色谱-质谱联用(LC-MS)技术检测大鼠膝关节软骨氨基酸代谢物表达。
结果:
2
与正常组比较,模型组膝关节软骨面粗糙,色泽暗沉,细胞出现簇集、核固缩及空泡样变性,内质网明显减少且结构异常,膝关节直径增加(
P
<
0.01),机械性痛阈值降低(
P
<
0.05),膝关节滑膜组织MMP-13和IL-1β含量均升高(
P
<
0.01),膝关节软骨脯氨酸、甘氨酸、赖氨酸、天冬氨酸、丙氨酸、甲硫氨酸、丝氨酸表达量升高(
P
<
0.05)。与模型组比较,艾灸组膝关节软骨组织损伤改善,膝关节直径降低(
P
<
0.01),机械性痛阈值升高(
P
<
0.05),膝关节滑膜组织MMP-13和IL-1β含量均降低(
P
<
0.05),膝关节软骨脯氨酸、甘氨酸、赖氨酸、天冬氨酸、组氨酸、谷氨酸表达量降低(
P
<
0.05)。
结论:
2
艾灸“足三里”能改善KOA模型大鼠膝关节肿胀、疼痛、软骨细胞损伤和滑膜炎症反应,可能通过甘氨酸、脯氨酸、赖氨酸和天冬氨酸等氨基酸代谢途径调控KOA免疫反应和软骨的合成与分解,发挥抗炎镇痛和软骨保护作用。
Objective
2
To observe the effect of moxibustion at "Zusanli" (ST36) on amino acid metabolism of knee cartilage in the rats with knee osteoarthritis (KOA)
and explore the mechanism of moxibustion for alleviating KOA cartilage injury.
Methods
2
Thirty male SD rats were randomly divided into a normal group
a model group
and a moxibustion group
10 rats in each one. The KOA models were prepared by injecting the mixed solution of L-cysteine and papain into the bilateral knee joint cavities of rats in the model group and the moxibustion group. In the moxibustion group
moxibustion was applied to bilateral "Zusanli" (ST36)
30 min each time
once daily and for consecutive 30 days. Before and after modeling
as well as after intervention
the knee joint diameter was measured. After intervention
the mechanical pain threshold was detected
the morphology of the cartilage tissue in the knee joint was observed using HE staining
and the ultrastructure of chondrocytes was observed under transmission electron microscopy; the levels of matrix metalloproteinase-13 (MMP-13) and interleukin-1β (IL-1β) in synovial tissue were detected using ELISA and the expression of cartilage amino acid metabolites was detected using liquid chromatography-mass spectrometry (LC-MS).
Results
2
Compared with the normal group
in the model group
the cartilage surface of the knee joint was rough and dark
the cells appeared clustering
nuclear pyknosis and vacuolar degeneration
the endoplasmic reticulum was obviously reduced and abnormal in structure; the diameter of the knee joint increased (
P
<
0.01)
the mechanical pain threshold decreased (
P
<
0.05)
the contents of MMP-13 and IL-1β in the knee joint synovium were elevated (
P
<
0.01)
and the expression levels of proline
glycine
lysine
aspartate
alanine
methionine
and seri
ne in the knee joint cartilage rose (
P
<
0.05). When compared with the model group
in the moxibustion group
the injury of knee cartilage tissue was alleviated
the diameter of knee joint was reduced (
P
<
0.01)
and the mechanical pain threshold was elevated (
P
<
0.05); the contents of MMP-13 and IL-1β in knee joint synovium decreased (
P
<
0.05)
and the expression levels of proline
glycine
lysine
aspartate
histidine
glutamate in knee joint cartilage decreased (
P
<
0.05).
Conclusion
2
Moxibustion at "Zusanli" (ST36) alleviates joint swelling
pain
chondrocyte injury
and synovitis in KOA model rats; and exerts its anti-inflammatory
analgesic
and cartilage protective effect by modulating immune response and synthesis and degradation of cartilage in KOA through metabolic pathways of amino acids such as glycine
proline
aspartate and lysine.
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