Volume 44 Issue 7
Jul.  2023
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Shaoyou DENG, Rong LI, Jintao LI, Yulan ZHAO, Peijin WANG, Hong ZHENG. Mechanism of Osteoking Improving Osteoarthritis based on Network Pharmacology and DDM Rats[J]. Journal of Kunming Medical University, 2023, 44(7): 34-39. doi: 10.12259/j.issn.2095-610X.S20230701
Citation: Shaoyou DENG, Rong LI, Jintao LI, Yulan ZHAO, Peijin WANG, Hong ZHENG. Mechanism of Osteoking Improving Osteoarthritis based on Network Pharmacology and DDM Rats[J]. Journal of Kunming Medical University, 2023, 44(7): 34-39. doi: 10.12259/j.issn.2095-610X.S20230701

Mechanism of Osteoking Improving Osteoarthritis based on Network Pharmacology and DDM Rats

doi: 10.12259/j.issn.2095-610X.S20230701
  • Received Date: 2023-03-27
    Available Online: 2023-07-17
  • Publish Date: 2023-07-25
  •   Objective   To explore the potential mechanism of Osteoking (OK) in the treatment of Osteoarthritis (OA) and preliminarily verify it with DMM rats.   Methods   TCMSP database was used to collect potential targets of OK, GeneCards database and OMIM were used to screen target genes related to OA, and Cytoscape 3.8.2 software was used to establish a regulatory network for interaction between OK Active ingredient and OA target genes. The STRING database was used to construct protein interaction maps and GO and KECG were analyzed. In addition, OA rats were constructed using medial meniscus instability surgery (DMM) to observe knee joint cartilage lesions, and ELISA was used to detect inflammation and oxidative stress levels after OK treatment.   Results  Network pharmacology results showed that 80 core genes were involved in OK therapy for OA, including serum albumin (ALB) and interleukin-6 (IL6), mainly involving biological processes such as immunity, inflammatory response, oxidative stress, and metabolism. Animal experiments showed that compared with the model group, the surface structure of the articular cartilage in the OK group of rats tended to be normal, with less detachment of chondrocytes; OK reduced serum inflammatory factors IL-6 (P < 0.01), VEGF (P < 0.01), and oxidative stress factor MDA (P < 0.05), improved ALB levels and SOD activity (P < 0.01).   Conclusion  OK can alleviate OA cartilage tissue damage, enhance immunity, and inhibit inflammation and oxidative stress reactions, preliminarily verifying the results of network pharmacology.
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