Evidence of subchondral bone’s effects on articular cartilage damage in OVX-OA rat
Evidence of subchondral bone’s effects on articular cartilage damage in OVX-OA rat
复制标题
软骨下骨对 OVX-OA 大鼠关节软骨损伤影响的证据
DOI:
10.1016/j.engfracmech.2020.107081
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发表时间:
2020-06
影响因子:
5.4
通讯作者:
Huijie Leng
中科院分区:
文献类型:
--
作者:
Zhenda Zhao;Qizhao Tan;Ai Jiang;Shang Sun;Zhongjun Liu;Weishi Li;Chunli Song;Huijie Leng
The role of subchondral bone in cartilage damage attracts increasing interests in osteoarthritis (OA) research. Subchondral bone might play more important roles in cartilage damage for postmenopausal women due to estrogen’s remarkable influence on bone metabolism. However, it still lacks direct evidence on the role of subchondral bone since estrogen can influence metabolisms of cartilage and subchondral bone at the same time. This study adopted the OVX-OA rat model. Damage scores and mechanical properties of cartilage and trabecular parameters of subchondral bone were evaluated. Change ratios of all the parameters at week 9 relative to week 3 which represented alterations after OVX were calculated. The results showed that change ratios of subchondral bone and cartilage damage in femur unit were both significantly lower than those in tibia unit. The two units were under the same estrogen level. That lower cartilage damage responded to lower subchondral bone change in femur unit provided evidence that articular cartilage damage might directly be affected by mechanical environmental changes induced by subchondral bone alteration in OVX-OA. Thus, for clinics, subchondral bone might be an new treatment target for this type of OA; for numerical simulation of articular joint, subchondral bone and cartilage shouldn’t be modeled as two independent parts.
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影响因子:
3.2
作者:
Stewart HL;Kawcak CE
通讯作者:
Kawcak CE
影响因子:
7
作者:
Srikanth, VK;Fryer, JL;Jones, G
通讯作者:
Jones, G
影响因子:
2.8
作者:
Alexandersen, P.;Karsdal, M. A.;Christiansen, C.
通讯作者:
Christiansen, C.
影响因子:
13.8
作者:
Zhen, Gehua;Cao, Xu
通讯作者:
Cao, Xu
影响因子:
2.3
作者:
Rieger R;Boulocher C;Kaderli S;Hoc T
通讯作者:
Hoc T