首页> 外文期刊>BioMed research international >Subchondral Bone Plate Thickening Precedes Chondrocyte Apoptosis and Cartilage Degradation in Spontaneous Animal Models of Osteoarthritis
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Subchondral Bone Plate Thickening Precedes Chondrocyte Apoptosis and Cartilage Degradation in Spontaneous Animal Models of Osteoarthritis

机译:骨关节炎自发动物模型中软骨下骨板增厚先于软骨细胞凋亡和软骨降解

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Osteoarthritis (OA) is the most common joint disorder characterised by bone remodelling and cartilage degradation and associated with chondrocyte apoptosis. These processes were investigated at 10, 16, 24, and 30 weeks in Dunkin Hartley (DH) and Bristol Strain 2 (BS2) guinea pigs that develop OA spontaneously. Both strains had a more pronounced chondrocyte apoptosis, cartilage degradation, and subchondral bone changes in the medial than the lateral side of the tibia, and between strains, the changes were always greater and faster in DH than BS2. In the medial side, a significant increase of chondrocyte apoptosis and cartilage degradation was observed in DH between 24 and 30 weeks of age preceded by a progressive thickening and stiffening of subchondral bone plate (Sbp). The Sbp thickness consistently increased over the 30-week study period but the bone mineral density (BMD) of the Sbp gradually decreased after 16 weeks. The absence of these changes in the medial side of BS2 may indicate that the Sbp of DH was undergoing remodelling. Chondrocyte apoptosis was largely confined to the deep zone of articular cartilage and correlated with thickness of the subchondral bone plate suggesting that cartilage degradation and chondrocyte apoptosis may be a consequence of continuous bone remodelling during the development of OA in these animal models of OA.
机译:骨关节炎(OA)是最常见的关节疾病,其特征是骨骼重塑和软骨降解,并伴有软骨细胞凋亡。在第10、16、24和30周时对自然发展为OA的Dunkin Hartley(DH)和Bristol Strain 2(BS2)豚鼠进行了研究。与胫骨外侧相比,这两种菌株在内侧的软骨细胞凋亡,软骨降解和软骨下骨变化都更为明显,并且菌株之间,DH的变化总是比BS2更大,更快。在内侧,在24至30周龄的DH中观察到软骨细胞凋亡和软骨降解显着增加,然后软骨下骨板(Sbp)逐渐变厚和变硬。在30周的研究期内,Sbp的厚度持续增加,但16周后,Sbp的骨矿物质密度(BMD)逐渐降低。 BS2内侧没有这些变化可能表明DH的Sbp正在重塑。软骨细胞凋亡在很大程度上局限在关节软骨的深部,并且与软骨下骨板的厚度相关,这表明在这些OA动物模型中,OA发育过程中软骨降解和软骨细胞凋亡可能是连续骨重塑的结果。

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