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本文引用的文献

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Posttraumatic osteoarthritis caused by battlefield injuries: the primary source of disability in warriors.战争创伤性骨关节炎:战士致残的首要原因。
J Am Acad Orthop Surg. 2012;20 Suppl 1(0 1):S64-9. doi: 10.5435/JAAOS-20-08-S64.
2
A polarized light microscopy method for accurate and reliable grading of collagen organization in cartilage repair.一种用于准确可靠地评估软骨修复中胶原组织分级的偏光显微镜方法。
Osteoarthritis Cartilage. 2011 Jan;19(1):126-35. doi: 10.1016/j.joca.2010.10.010. Epub 2010 Oct 16.
3
Organ-level histological and biomechanical responses from localized osteoarticular injury in the rabbit knee.兔膝关节局灶性骨关节炎损伤的组织学和生物力学反应。
J Orthop Res. 2011 Mar;29(3):340-6. doi: 10.1002/jor.21259. Epub 2010 Sep 30.
4
Histopathology atlas of animal model systems - overview of guiding principles.动物模型系统的组织病理学图谱 - 指导原则概述。
Osteoarthritis Cartilage. 2010 Oct;18 Suppl 3:S2-6. doi: 10.1016/j.joca.2010.07.013.
5
Basic methods in histopathology of joint tissues.关节组织病理组织学的基本方法。
Osteoarthritis Cartilage. 2010 Oct;18 Suppl 3:S113-6. doi: 10.1016/j.joca.2010.05.026.
6
Cartilage, bone and synovial histomorphometry in animal models of osteoarthritis.骨关节炎动物模型中的软骨、骨和滑膜组织形态计量学。
Osteoarthritis Cartilage. 2010 Oct;18 Suppl 3:S106-12. doi: 10.1016/j.joca.2010.05.024.
7
The OARSI histopathology initiative - the tasks and limitations.骨关节炎研究学会国际联盟(OARSI)组织病理学倡议——任务与局限性
Osteoarthritis Cartilage. 2010 Oct;18 Suppl 3:S1. doi: 10.1016/j.joca.2010.04.018.
8
Oxidant conditioning protects cartilage from mechanically induced damage.氧化剂预处理能保护软骨免受机械损伤。
J Orthop Res. 2010 Jul;28(7):914-20. doi: 10.1002/jor.21072.
9
N-acetylcysteine inhibits post-impact chondrocyte death in osteochondral explants.N-乙酰半胱氨酸可抑制骨软骨外植体撞击后软骨细胞的死亡。
J Bone Joint Surg Am. 2009 Aug;91(8):1890-7. doi: 10.2106/JBJS.H.00545.
10
Biomechanical, biochemical and structural correlations in immature and mature rabbit articular cartilage.未成熟和成熟兔关节软骨的生物力学、生化和结构相关性。
Osteoarthritis Cartilage. 2009 Dec;17(12):1628-38. doi: 10.1016/j.joca.2009.07.002. Epub 2009 Jul 8.

人类与常见骨关节炎模型的数字化软骨组织学比较

Comparative digital cartilage histology for human and common osteoarthritis models.

作者信息

Pedersen Douglas R, Goetz Jessica E, Kurriger Gail L, Martin James A

机构信息

Department of Orthopaedics and Rehabilitation, University of Iowa, Iowa City, IA, USA.

出版信息

Orthop Res Rev. 2013 Feb 12;2013(5):13-20. doi: 10.2147/ORR.S38400.

DOI:10.2147/ORR.S38400
PMID:24465137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3899351/
Abstract

PURPOSE

This study addresses the species-specific and site-specific details of weight-bearing articular cartilage zone depths and chondrocyte distributions among humans and common osteoarthritis (OA) animal models using contemporary digital imaging tools. Histological analysis is the gold-standard research tool for evaluating cartilage health, OA severity, and treatment efficacy. Historically, evaluations were made by expert analysts. However, state-of-the-art tools have been developed that allow for digitization of entire histological sections for computer-aided analysis. Large volumes of common digital cartilage metrics directly complement elucidation of trends in OA inducement and concomitant potential treatments.

MATERIALS AND METHODS

Sixteen fresh human knees, 26 adult New Zealand rabbit stifles, and 104 bovine lateral plateaus were measured for four cartilage zones and the cell densities within each zone. Each knee was divided into four weight-bearing sites: the medial and lateral plateaus and femoral condyles.

RESULTS

One-way analysis of variance followed by pairwise multiple comparisons (Holm-Sidak method at a significance of 0.05) clearly confirmed the variability between cartilage depths at each site, between sites in the same species, and between weight-bearing articular cartilage definitions in different species.

CONCLUSION

The present study clearly demonstrates multisite, multispecies differences in normal weight-bearing articular cartilage, which can be objectively quantified by a common digital histology imaging technique. The clear site-specific differences in normal cartilage must be taken into consideration when characterizing the pathoetiology of OA models. Together, these provide a path to consistently analyze the volume and variety of histologic slides necessarily generated by studies of OA progression and potential treatments in different species.

摘要

目的

本研究使用当代数字成像工具,探讨人类和常见骨关节炎(OA)动物模型中负重关节软骨区域深度和软骨细胞分布的物种特异性及部位特异性细节。组织学分析是评估软骨健康状况、OA严重程度和治疗效果的金标准研究工具。以往,评估由专家分析师进行。然而,现已开发出先进工具,可将整个组织学切片数字化以进行计算机辅助分析。大量常见的数字软骨指标直接有助于阐明OA诱发趋势及相关潜在治疗方法。

材料与方法

对16个新鲜人类膝关节、26个成年新西兰兔膝关节和104个牛外侧平台的四个软骨区域及其每个区域内的细胞密度进行测量。每个膝关节分为四个负重部位:内侧和外侧平台以及股骨髁。

结果

采用单因素方差分析,随后进行两两多重比较(Holm-Sidak方法,显著性水平为0.05),明确证实了各部位软骨深度之间、同一物种不同部位之间以及不同物种负重关节软骨定义之间的变异性。

结论

本研究清楚地表明正常负重关节软骨存在多部位、多物种差异,可通过一种常见的数字组织学成像技术进行客观量化。在描述OA模型的病理病因时,必须考虑正常软骨中明显的部位特异性差异。这些共同为持续分析不同物种OA进展和潜在治疗研究必然产生的组织学切片的数量和种类提供了途径。