Efficacy of zoledronic acid in treatment of teoarthritis is dependent on the disease progression stage in rat medial meniscal tear model
Efficacy of zoledronic acid in treatment of teoarthritis is dependent on the disease progression stage in rat medial meniscal tear model
复制标题
唑来膦酸治疗骨关节炎的疗效取决于大鼠内侧半月板撕裂模型中的疾病进展阶段
DOI:
10.1038/aps.2012.28
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发表时间:
2012-05
影响因子:
8.2
通讯作者:
Nie, Shao-bo
中科院分区:
文献类型:
--
作者:
Yu, De-gang;Liu, Shen;Zhu, Zhen-an;Yu, Bo;Mao, Yuan-qing;Zhao, Xin;Wang, Xiao-qing;Ding, Hui-feng;Cao, Lei;Liu, Guang-wang;Nie, Shao-bo
Aim:To investigate whether the stage of osteoarthritis (OA) progression influenced the efficacy of the third-generation bisphosphonate zoledronic acid in a rat medial meniscal tear model.Methods:Medial meniscal tear (MMT) was surgically induced in adult male Sprague Dawley rats. Zoledronic acid (ZOL, 100 μg/kg, sc, twice a week) was administered starting immediately, early (from 4 weeks) or late (from 8 weeks) after OA induction. The degeneration of articular cartilage was evaluated with toluidine blue O staining. Subchondral bone remodeling was evaluated with X-ray micro-CT scanning. Joint pain was measured with respect to weight-bearing asymmetry. Calcitonin gene-related peptide (CGRP) expression in dorsal root ganglia (DRGs) was examined using immunofluorescence analysis. The afferent neurons in DRGs innervating the joint were identified by retrograde labeling with fluorogold.Results:Progressive cartilage loss was observed during 12 weeks after OA induction. Subchondral bone remodeling manifested as increased bone resorption at early stage (4 weeks), but as increased bone accretion at advanced stages (8 weeks). Immediately and early ZOL administration significantly improved subchondral microstructural parameters, attenuated cartilage degeneration, reduced weight-bearing asymmetry and CGRP expression, whereas the late ZOL administration had no significant effects.Conclusion:The stage of OA progression influences the efficacy of ZOL in treating joint degeneration and pain. To obtain the maximum efficacy, bisphosphonate treatment should be initiated in rat with early stages of OA pathogenesis.
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影响因子:
--
作者:
Moisio, Kirsten;Eckstein, Felix;Chmiel, Joan S.;Guermazi, Ali;Prasad, Pottumarthi;Almagor, Orit;Song, Jing;Dunlop, Dorothy;Hudelmaier, Martin;Kothari, Ami;Sharma, Leena
通讯作者:
Sharma, Leena
DOI:
10.1016/j.berh.2009.08.004
发表时间:
2010-02-01
影响因子:
5.2
作者:
Tat, Steeve Kwan;Lajeunesse, Daniel;Martel-Pelletier, Johanne
通讯作者:
Martel-Pelletier, Johanne
DOI:
--
发表时间:
1997-10
期刊:
The Western journal of medicine
影响因子:
--
作者:
H. Holman;K. Lorig
通讯作者:
H. Holman;K. Lorig
影响因子:
7
作者:
Lindsey, CT;Narasimhan, A;Majumdar, S
通讯作者:
Majumdar, S
DOI:
10.1002/art.1790060105
发表时间:
1993-03
期刊:
Arthritis care and research : the official journal of the Arthritis Health Professions Association
影响因子:
--
作者:
Sarah E. Hampson;Russell E. Glasgow;Antonette M. Zeiss;Stephen F Birskovich;Lyn S. Foster;Alana Lines
通讯作者:
Sarah E. Hampson;Russell E. Glasgow;Antonette M. Zeiss;Stephen F Birskovich;Lyn S. Foster;Alana Lines