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本文引用的文献

1
Musculoskeletal changes following non-invasive knee injury using a novel mouse model of post-traumatic osteoarthritis.使用一种新型创伤后骨关节炎小鼠模型研究非侵入性膝关节损伤后的肌肉骨骼变化。
Osteoarthritis Cartilage. 2012 Jul;20(7):773-82. doi: 10.1016/j.joca.2012.04.014. Epub 2012 Apr 21.
2
Changes in subchondral bone early in the development of osteoarthritis.骨关节炎早期软骨下骨的变化。
Arthritis Rheum. 2011 Sep;63(9):2561-3. doi: 10.1002/art.30306.
3
Osteoporotic changes of subchondral trabecular bone in osteoarthritis of the knee: a 3-T MRI study.膝关节骨关节炎中软骨下骨小梁的骨质疏松变化:3T MRI 研究。
Osteoporos Int. 2012 Feb;23(2):589-97. doi: 10.1007/s00198-011-1585-2. Epub 2011 Feb 26.
4
Multimodal imaging demonstrates concomitant changes in bone and cartilage after destabilisation of the medial meniscus and increased joint laxity.多模态成像显示内侧半月板不稳定和关节松弛增加后,骨和软骨同时发生变化。
Osteoarthritis Cartilage. 2011 Feb;19(2):163-70. doi: 10.1016/j.joca.2010.11.006. Epub 2010 Nov 19.
5
Characterizing a novel and adjustable noninvasive murine joint loading model.表征一种新型可调节的无创小鼠关节加载模型。
Arthritis Rheum. 2011 Jan;63(1):137-47. doi: 10.1002/art.27765.
6
The OARSI histopathology initiative - recommendations for histological assessments of osteoarthritis in the mouse.骨关节炎研究协会组织病理学倡议——推荐用于评估小鼠骨关节炎的组织学评估方法。
Osteoarthritis Cartilage. 2010 Oct;18 Suppl 3:S17-23. doi: 10.1016/j.joca.2010.05.025.
7
Guidelines for assessment of bone microstructure in rodents using micro-computed tomography.骨组织形态计量学分析的鼠类骨骼microCT 评估指南
J Bone Miner Res. 2010 Jul;25(7):1468-86. doi: 10.1002/jbmr.141.
8
Knee osteoarthritis after anterior cruciate ligament injury: a systematic review.前交叉韧带损伤后膝关节骨关节炎:一项系统评价
Am J Sports Med. 2009 Jul;37(7):1434-43. doi: 10.1177/0363546509338827.
9
Avulsion fractures of the knee: imaging findings and clinical significance.膝关节撕脱骨折:影像学表现及临床意义
Radiographics. 2008 Oct;28(6):1755-70. doi: 10.1148/rg.286085503.
10
Radiographic evaluation of arthritis: degenerative joint disease and variations.关节炎的影像学评估:退行性关节病及变异
Radiology. 2008 Sep;248(3):737-47. doi: 10.1148/radiol.2483062112.

加载率依赖性损伤模式在创伤后骨关节炎小鼠模型中的比较。

Comparison of loading rate-dependent injury modes in a murine model of post-traumatic osteoarthritis.

机构信息

Department of Orthopaedic Surgery, University of California-Davis Medical Center, 4635 2nd Ave, Suite 2000, Sacramento, California, 95817.

出版信息

J Orthop Res. 2014 Jan;32(1):79-88. doi: 10.1002/jor.22480. Epub 2013 Sep 9.

DOI:10.1002/jor.22480
PMID:24019199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4140447/
Abstract

Post-traumatic osteoarthritis (PTOA) is a common long-term consequence of joint injuries such as anterior cruciate ligament (ACL) rupture. In this study we used a tibial compression overload mouse model to compare knee injury induced at low speed (1 mm/s), which creates an avulsion fracture, to injury induced at high speed (500 mm/s), which induces midsubstance tear of the ACL. Mice were sacrificed at 0 days, 10 days, 12 weeks, or 16 weeks post-injury, and joints were analyzed with micro-computed tomography, whole joint histology, and biomechanical laxity testing. Knee injury with both injury modes caused considerable trabecular bone loss by 10 days post-injury, with the Low Speed Injury group (avulsion) exhibiting a greater amount of bone loss than the High Speed Injury group (midsubstance tear). Immediately after injury, both injury modes resulted in greater than twofold increases in total AP joint laxity relative to control knees. By 12 and 16 weeks post-injury, total AP laxity was restored to uninjured control values, possibly due to knee stabilization via osteophyte formation. This model presents an opportunity to explore fundamental questions regarding the role of bone turnover in PTOA, and the findings of this study support a biomechanical mechanism of osteophyte formation following injury.

摘要

创伤后骨关节炎(PTOA)是关节损伤(如前交叉韧带(ACL)断裂)的常见长期后果。在这项研究中,我们使用胫骨压缩过载小鼠模型比较了低速(1mm/s)引起的膝关节损伤,这种损伤会导致撕脱性骨折,以及高速(500mm/s)引起的 ACL 中段撕裂。小鼠在损伤后 0 天、10 天、12 周或 16 周时被处死,并用微计算机断层扫描、全关节组织学和生物力学松弛度测试对关节进行分析。两种损伤模式都在损伤后 10 天内导致了相当大的小梁骨丢失,低速损伤组(撕脱)比高速损伤组(中段撕裂)表现出更多的骨丢失。损伤后立即,与对照膝关节相比,两种损伤模式的总 AP 关节松弛度增加了两倍以上。到损伤后 12 周和 16 周时,总 AP 松弛度恢复到未受伤的对照值,这可能是由于骨赘形成导致膝关节稳定。该模型为探索骨转换在 PTOA 中的作用的基本问题提供了机会,本研究的结果支持损伤后骨赘形成的生物力学机制。