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[磷酸化粘着斑激酶、磷脂酰肌醇3激酶及聚集蛋白聚糖基因和蛋白在软骨细胞中可能参与针刀干预诱导兔膝骨关节炎病情改善]

[Phosphorylated Focal Adhesion Kinase, Phosphinositides 3 Kinase and Aggrecan Genes and Proteins in Cartilage Cells Are Probably Involved in Needle Knife Intervention Induced Improvement of Knee Osteoarthritis in Rabbits].

作者信息

Liu Nai-Gang, Yu Jia-Ni, Hu Bo, Guo Yan, Guo Chang-Qing

机构信息

Department of Acupuncture-moxibustion, China-Japan Friendship Hospital, Beijing 100029, China.

Department of Rehabilitation, Guangdong Hospital of Traditional Chinese Medicine, Guangzhou 510120.

出版信息

Zhen Ci Yan Jiu. 2018 Apr 25;43(4):221-5. doi: 10.13702/j.1000-0607.170890.

Abstract

OBJECTIVE

We have demonstrated that needle knife (acupotomy) treatment can improve knee osteoarthritis (KOA) in rabbits. The present study was designed to examine its effect on expression of phosphorylated focal adhesion kinase (p-FAK), phosphinositides 3 kinase (p-PI 3 K) and Aggrecan genes and proteins in the knee-joint cartilage tissues of KOA rabbits, so as to explore its partial molecular mechanism underlying improvement of KOA.

METHODS

Forty-nine New Zealand male rabbits were randomly divided into normal control, model, model +inhibitor, needle knife, needle knife+ inhibitor, electroacupuncture (EA), EA +inhibitor groups (=7 in each). The KOA model was established by modified Videman method (left hindlimb extension immobilization and ankle dorsal flexion 60°). Acupotomy relaxing manipulation was applied to the lateral collateral ligament and patellar ligament of the left knee-joint, two times a week for 4 weeks, and EA (2 Hz/100 Hz, 3 mA) was applied to the left "Liangmen" (ST 21), "Xuehai" (SP 10), "Neixiyan " (EX-LE 4) and "Dubi" (ST 35) for 20 min, three times a week, for 4 weeks. About 2 h before every needle-knife or EA treatment or at the corresponding time-point, intra-articular cavity injection of PF-562271(a specific antagonist of FAK, 200 μmol/L, 0.5 mL)was performed in the three inhibitor groups. The expression levels of p-FAK, p-PI 3 K, Aggrecan genes and proteins in the cartilage tissues were measured with quantitative Real-time PCR and Western blot, separately.

RESULTS

After modeling, the expression levels of p-FAK and p-PI 3 K genes and proteins were significantly up-regulated (<0.05, <0.01), while those of Aggrecan protein and mRNA considerably down-regulated in the model group in comparison with the normal group (<0.01). Following 4 weeks' needle-knife or EA treatment, the expression levels of p-FAK and p-PI 3 K and Aggrecan proteins in both EA and needle-knife groups, and Aggrecan mRNA in the needle knife group were significantly up-regulated (<0.05, <0.01). After administration of p-FAK antagonist, modeling-induced upregulation of expression of p-FAK mRNA and protein and p-PI 3 K protein, as well as modeling-induced down-regulation of Aggrecan mRNA and protein were significantly suppressed in the model+inhibitor group (<0.05, <0.01), and needle knife-induced and EA-induced up-regulation of expression of p-FAK, p-PI 3 K and Aggrecan mRNAs and proteins was notably suppressed respectively in comparison with the needle knife and EA groups (<0.05, <0.01). The effect of needle knife was significantly superior to that of EA in up-regulating p-PI 3 K and Aggrecan mRNAs as well as p-FAK, p-PI 3 K and Aggrecan proteins (<0.05, <0.01).

CONCLUSION

Needle knife intervention can up-regulate the expression levels of p-FAK, p-PI 3 K and Aggrecan proteins and mRNAs in the cartilage tissue of the knee-joint in KOA rabbits, suggesting an involvement of FAK-PI 3 K signaling in the needle knife-induced improvement of KOA.

摘要

目的

我们已证明针刀(小针刀)治疗可改善兔膝骨关节炎(KOA)。本研究旨在探讨其对KOA兔膝关节软骨组织中磷酸化粘着斑激酶(p-FAK)、磷脂酰肌醇3激酶(p-PI 3 K)及聚集蛋白聚糖基因和蛋白表达的影响,以探究其改善KOA的部分分子机制。

方法

49只新西兰雄性兔随机分为正常对照组、模型组、模型+抑制剂组、针刀组、针刀+抑制剂组、电针(EA)组、EA+抑制剂组(每组7只)。采用改良的Videman法(左后肢伸直固定,踝关节背屈60°)建立KOA模型。对左膝关节外侧副韧带和髌韧带进行针刀松解术,每周2次,共4周;对左侧“梁门”(ST 21)、“血海”(SP 10)、“内膝眼”(EX-LE 4)和“犊鼻”(ST 35)施加电针(2 Hz/100 Hz,3 mA),每次20分钟,每周3次,共4周。在每次针刀或电针治疗前约2小时或相应时间点,对三个抑制剂组进行关节腔内注射PF-562271(FAK的特异性拮抗剂,200 μmol/L,0.5 mL)。分别采用定量实时PCR和蛋白质印迹法检测软骨组织中p-FAK、p-PI 3 K、聚集蛋白聚糖基因和蛋白的表达水平。

结果

建模后,与正常组相比,模型组中p-FAK和p-PI 3 K基因及蛋白表达水平显著上调(<0.05,<0.01),而聚集蛋白聚糖蛋白和mRNA水平显著下调(<0.01)。经过4周的针刀或电针治疗后,电针组和针刀组中p-FAK、p-PI 3 K及聚集蛋白聚糖蛋白表达水平,以及针刀组中聚集蛋白聚糖mRNA水平均显著上调(<0.05,<0.01)。给予p-FAK拮抗剂后,模型+抑制剂组中建模诱导的p-FAK mRNA和蛋白及p-PI 3 K蛋白表达上调,以及建模诱导的聚集蛋白聚糖mRNA和蛋白表达下调均受到显著抑制(<0.05,<0.01),与针刀组和电针组相比,针刀诱导和电针诱导的p-FAK、p-PI 3 K及聚集蛋白聚糖mRNA和蛋白表达上调分别受到显著抑制(<0.05,<0.01)。在上调p-PI 3 K和聚集蛋白聚糖mRNA以及p-FAK、p-PI 3 K和聚集蛋白聚糖蛋白方面,针刀的效果显著优于电针(<0.05,<0.01)。

结论

针刀干预可上调KOA兔膝关节软骨组织中p-FAK、p-PI 3 K及聚集蛋白聚糖蛋白和mRNA的表达水平,提示FAK-PI 3 K信号通路参与了针刀诱导的KOA改善过程。

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