Chinese Journal of Tissue Engineering Research ›› 2020, Vol. 24 ›› Issue (8): 1188-1194.doi: 10.3969/j.issn.2095-4344.2014

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Effect of Psammosilene gavage on the expression of apoptosis-related proteins in chondrocytes of a rabbit osteoarthritis model  

Peng Xu1, Yang Jibin2, You Qi2, Jin Ying2, Zhang Jun2, Ge Zhen2, Zou Gang2, Jiang Kongjun2, Liu Yi2   

  1. 1Department of Joint Surgery, Suining Central Hospital, Suining 629000, Sichuan Province, China; 2First Department of Orthopedics, the Affiliated Hospital of Zunyi Medical University, Zunyi 563000, Guizhou Province, China
  • Received:2019-05-07 Revised:2019-05-21 Accepted:2019-06-27 Online:2020-03-18 Published:2020-01-20
  • Contact: Liu Yi, Professor, Master’s supervisor, First Department of Orthopedics, the Affiliated Hospital of Zunyi Medical University, Zunyi 563000, Guizhou Province, China
  • About author:Peng Xu, Master, Department of Joint Surgery, Suining Central Hospital, Suining 629000, Sichuan Province, China
  • Supported by:
    the Combined Project of Science and Technology Department of Guizhou Province, No. [2017]7015; a grant from the Administration of Traditional Chinese Medicine of Guizhou Province, No. QYZZ-2016-029

Abstract:

BACKGROUND: Psammosilene Capsule is a traditional Miao medicine formula that consists of Psammosilene tunicoides and Schefflera kwangsiensis. Psammosilene Capsule has been shown to hold protective effect on cartilage, but the underlying mechanism remains unclear.

OBJECTIVE: To explore the possible mechanism of Psammosilene gavage in the treatment of osteoarthritis.

METHODS: Ten of the 40 rabbits were randomly selected as the blank control group. The remaining 30 rabbits were used to establish the osteoarthritis model in the right hind knee of the rabbit by the modified Hulth method, and then were randomly divided into model (n=10), Psammosilene gavage (n=10), and p38 inhibitor (n=10) groups. At 7 days after modeling, the Psammosilene gavage group was fed with Psammosilene (57.5 mg/kg per day, p38 inhibitor group was injected with p38 inhibitor into the right hind knee joint (SB203580, 10 μmol/L, 0.5 mL), once weekly. The blank control and model groups were given the same amount of clean water, once daily. After 8 weeks, all animals were sacrificed to remove the right hind knee femoral condyle and tibial plateau. Severity of cartilage injury was evaluated by Pelletier score. Cartilage degeneration was examined by hematoxylin-eosin staining, saffron O staining and Mankin score. The expression levels of P-p38 and Cleaved Caspase-3 protein in cartilage tissue were detected by western blot assay. The expression levels of Bcl-2 and Bax mRNA in cartilage tissues were detected by quantitative real-time PCR.

RESULTS AND CONCLUSION: (1) Compared with the Psammosilene gavage group, the model and p38 inhibitor groups had significantly increased Pelletier and Mankin scores (P < 0.05). (2) Compared with the Psammosilene gavage group, the expression levels of Bax mRNA and Cleaved Caspase-3 protein in the cartilage tissue in the model and p38 inhibitor groups were significantly increased (P < 0.05). (3) Compared with the Psammosilene gavage group, the expression level of Bcl-2 mRNA in the cartilage tissue in the model and p38 inhibitor groups was significantly decreased (P < 0.05). (4) Compared with the Psammosilene gavage group, the expression level of P-p38 protein in the model and p38 inhibitor groups was significantly increased (< 0.05). (5) Our findings suggest that Psammosilene can inhibit the expression of apoptosis-related proteins and P-p38 protein in cartilage tissue, and then delay the degeneration of articular cartilage in the rabbit osteoarthritis model.

Key words: osteoarthiritis, cartilage injury, Psammosilene, cell apoptosis, mitogen-activated protein kinases

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