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首页> 外文期刊>Journal of Hainan Medical University >Study on the relationship between PI3K/AKT signaling pathway and apoptosis in cartilage tissue of rats with osteoarthritis
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Study on the relationship between PI3K/AKT signaling pathway and apoptosis in cartilage tissue of rats with osteoarthritis

机译:PI3K / AKT信号通路与骨关节炎大鼠软骨组织细胞凋亡关系的研究

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Objective: To study the relationship between PI3K/AKT signaling pathway and apoptosis incartilage tissue of rats with osteoarthritis (OA). Methods: The clean male Wistar rats wereselected as experimental animals and randomly divided into OA model group and controlgroup. The OA model was established by intra-articular injection of papain solution andL-cysteine. Fourth weeks and eighth weeks after model establishment, the expression ofPI3K/AKT signaling molecules, inflammatory mediators, apoptosis marker molecules andautophagy marker molecules in articular cartilage were determined. Results: p-PI3K andp-AKT expression in articular cartilage of OA group were significantly lower than those ofcontrol group; IL-1β, IL-6, IL-17, IL-18, eIF4E, Bax, Caspase-3, mTOR, Beclin1, Atg5and Atg7 expression in articular cartilage of OA group were significantly higher than thoseof control group and negatively correlated with p-PI3K and p-AKT expression while Bcl-2expression in articular cartilage of OA group was significantly lower than that of control groupand positively correlated with p-PI3K and p-AKT expression. Conclusion: The inhibition ofPI3K/AKT signaling pathway in cartilage tissue of OA rat model can promote chondrocyteapoptosis and autophagy.
机译:目的:探讨PI3K / AKT信号通路与骨关节炎(OA)大鼠软骨组织凋亡的关系。方法:选择干净的雄性Wistar大鼠为实验动物,随机分为OA模型组和对照组。通过关节内注射木瓜蛋白酶溶液和L-半胱氨酸建立OA模型。建立模型后第4周和第8周,测定关节软骨中PI3K / AKT信号分子,炎症介质,细胞凋亡标记分子和自噬标记分子的表达。结果:OA组关节软骨中p-PI3K和p-AKT的表达明显低于对照组。 OA组关节软骨中IL-1β,IL-6,IL-17,IL-18,eIF4E,Bax,Caspase-3,mTOR,Beclin1,Atg5和Atg7的表达明显高于对照组,与p-负相关。 OA组关节软骨中PI3K和p-AKT的表达而Bcl-2的表达明显低于对照组,且与p-PI3K和p-AKT的表达呈正相关。结论:抑制OA大鼠模型软骨组织中PI3K / AKT信号通路可促进软骨细胞凋亡和自噬。

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