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机构地区:[1]上海交通大学附属第一人民医院,上海200080
出 处:《现代生物医学进展》2012年第7期1223-1224,1235,共3页Progress in Modern Biomedicine
基 金:国家自然科学基金项目(30700853)
摘 要:目的:建立早期股骨头坏死模型,为研究其发病机制及合理治疗方法的提供可靠的模型基础。方法:用单一剂量脂多糖LPS(10μg/kg)联合三次甲强龙MPS(10 mg/kg)注射,每次间隔24h,诱导建立兔早期股骨头坏死模型,通过影像学及组织病理性学方法评估模型建立情况。结果:4周后,模型组死亡1例,模型组16例X线检查未见异常表现,2例X线提示股骨头密度不均,未出现股骨头塌陷,18例HE染色示骨细胞空骨陷窝增多,脂肪细胞体积变大,数量增多。结论:用脂多糖(LPS)联合甲强龙可成功诱导建立兔早期股骨头坏死模型,模型成功率高、死亡率低。Objective: To construct the model of first-stage steroid-induced osteonecrosis in rabbits and prepare to seek for pathogenesis and rational treatment of first-stage osteonecrosis of femoral head.Methods: We constructed the model with lipopolys-accharide(signal-dose 10ug/kg) plus methylprodnisolone(10mg/kg,three times every 24h internals).The osteonecrosis model was evaluated by X-ray examination and hematoxylin and eosin stain.Results: In model group,two samples were featured with uneven density of femoral head in X-ray photograph.There were 18 samples with increased numbers of empty bone lacunae and larger quantity of fat cells compared with normal grop under light microscopy and histological.Conclsion: The animal model was induced by LPS plus MPS,with a high success rate and low mortality.
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