Animal models of osteonecrosis

被引:10
作者
Jones L.C. [1 ]
Allen M.R. [2 ]
机构
[1] Department of Orthopaedic Surgery, Johns Hopkins Orthopaedics at Good Samaritan Hospital, Smyth Building, Baltimore, MD 21239
[2] Department of Anatomy and Cell Biology, Indiana University School of Medicine, Indianapolis, IN
来源
Clinical Reviews in Bone and Mineral Metabolism | 2011年 / 9卷 / 1期
关键词
Animal models; Corticosteroids; Legg-Calve-Perthes disease; ONJ; Osteonecrosis; Osteonecrosis of the jaw;
D O I
10.1007/s12018-011-9090-x
中图分类号
学科分类号
摘要
Osteonecrosis is an uncommon but significant musculoskeletal disease characterized by focal areas of dead bone that often fail to heal even with intervention and has the potential to negatively impact a patient's quality of life. The knee and hip seem to be most susceptible to osteonecrosis although certain conditions, such as bisphosphonate treatment, have been associated with the development of osteonecrosis that is confined to the jaw. For most types of osteonecrosis, there remains much to be learned about either the pathophysiology of disease or the best course of treatment-questions that are best approached using an animal model. The different etiologies of the subclasses of osteonecrosis have led to a diverse number of animal models within the field. While no one animal model completely simulates all aspects of a particular type of osteonecrosis, models do exist that mimic various clinical aspects of osteonecrosis. This review discusses aspects of the common and novel animal models used to study juvenile osteonecrosis (Legg-Calvé-Perthes), trauma-induced osteonecrosis, alcohol- and corticosteroid-induced osteonecrosis, and osteonecrosis of the jaw associated with anti-remodeling drug treatment. © 2011 Springer Science+Business Media, LLC.
引用
收藏
页码:63 / 80
页数:17
相关论文
共 138 条
[11]  
Zahir A., Freeman M.A., Experimental stimulation of Perthes' disease in the puppy, Proc R Soc Med, 64, 6, pp. 641-642, (1971)
[12]  
Freeman M.A., England J.P., Experimental infarction of the immature canine femoral head, Proc R Soc Med, 62, 5, pp. 431-433, (1969)
[13]  
Mizuno S., Et al., Pathological histology of the Legg-Calve-Perthes disease with a special reference to its experimental production, Med J Osaka Univ, 17, 2, pp. 177-209, (1966)
[14]  
Li W., Et al., An animal model of Perthes disease and an experimental research of VEGF expression, Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi, 22, 7, pp. 814-819, (2008)
[15]  
Kamegaya M., Shinada Y., Akita T., Ogata S., Someya M., Tsuchiya K., Experimental avascular necrosis of the femoral capital epiphysis and induced subluxation of the hip in young rabbits, Journal of Pediatric Orthopaedics, 10, 1, pp. 1-5, (1990)
[16]  
Rowe S.M., Et al., The effects of subluxation of the femoral head with avascular necrosis in growing rabbits, J Pediatr Orthop, 24, 6, pp. 645-650, (2004)
[17]  
Kim H.K., Su P.H., Qiu Y.S., Histopathologic changes in growth-plate cartilage following ischemic necrosis of the capital femoral epiphysis. An experimental investigation in immature pigs, J Bone Joint Surg Am, 83, 5, pp. 688-697, (2001)
[18]  
Kim H.K.W., Bian H., Randall T., Garces A., Gerstenfeld L.C., Einhorn T.A., Increased VEGF expression in the epiphyseal cartilage after ischemic necrosis of the capital femoral epiphysis, Journal of Bone and Mineral Research, 19, 12, pp. 2041-2048, (2004)
[19]  
Kim H.K., Et al., Effects of disruption of epiphyseal vasculature on the proximal femoral growth plate, J Bone Joint Surg Am, 91, 5, pp. 1149-1158, (2009)
[20]  
Rowe S.M., Et al., Deformity of the femoral head following vascular infarct in piglets, Acta Orthop, 77, 1, pp. 33-38, (2006)