• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[糖皮质激素诱导性坏死兔股骨头血管的病理变化]

[Pathological changes of the blood vessels in rabbit femoral head with glucocorticoid-induced necrosis].

作者信息

Hu Zhi-ming, Wang Hai-bin, Zhou Ming-qian, Yao Xin-sheng, Ma Li, Wang Xiao-ning

机构信息

Institute of Molecular Immunology, Southern Medical University, Guangzhou 510515, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2006 Jun;26(6):785-7.

PMID:16793601
Abstract

OBJECTIVE

To observe the pathological changes in the blood vessels in rabbit femoral head with glucocorticoid-induced necrosis and investigate the pathogenesis of glucocorticoid-induced osteonecrosis.

METHODS

Twenty New Zealand white rabbits were randomly divided into two groups, namely group A. which was injected with horse serum and prednisone and group B as the control group. Chinese ink was injected into the femoral cavity of the rabbits to observe the blood vessels in the femoral head under optical microscope and the femoral head was examined histopathologically.

RESULTS

Compared with the normal control group, the rabbits in group A had significantly decreased number of perfused vessels, which was featured by defective perfusion, osteocytie pyknosis or necrosis, increase of empty ostoocyte lacunae and fat cells, decrease of hematopoietic tissue, and blood vessel occlusion.

CONCLUSION

Vascular occlusion and vasculitis due to glucocorticoid treatment may cause avascular necrosis of the femoral head.

摘要

目的

观察糖皮质激素诱导的兔股骨头坏死血管的病理变化,探讨糖皮质激素性骨坏死的发病机制。

方法

将20只新西兰白兔随机分为两组,即A组,注射马血清和泼尼松;B组为对照组。向兔股腔内注入中国墨汁,在光学显微镜下观察股骨头血管,并进行股骨头组织病理学检查。

结果

与正常对照组相比,A组兔灌注血管数量明显减少,表现为灌注不良、骨细胞固缩或坏死、空骨陷窝和脂肪细胞增多、造血组织减少以及血管闭塞。

结论

糖皮质激素治疗导致的血管闭塞和血管炎可能引起股骨头缺血性坏死。

相似文献

1
[Pathological changes of the blood vessels in rabbit femoral head with glucocorticoid-induced necrosis].[糖皮质激素诱导性坏死兔股骨头血管的病理变化]
Nan Fang Yi Ke Da Xue Xue Bao. 2006 Jun;26(6):785-7.
2
[Experimental study on avascular necrosis of femoral head induced by methylprednisolone combined with lipopolysaccharide in rabbits].甲基强的松龙联合脂多糖诱导兔股骨头缺血性坏死的实验研究
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2008 Mar;22(3):265-70.
3
[Effect of vascular endothelial growth factor and tumor necrosis factor receptor for treatment of avascular necrosis of the femoral head in rabbits].[血管内皮生长因子与肿瘤坏死因子受体对兔股骨头缺血性坏死的治疗作用]
Nan Fang Yi Ke Da Xue Xue Bao. 2008 Dec;28(12):2177-9.
4
[Changes of blood vessels in glucocorticoid-induced avascular necrosis of femoral head in rabbits].[糖皮质激素诱导的兔股骨头缺血性坏死中血管的变化]
Zhonghua Wai Ke Za Zhi. 2000 Mar;38(3):212-5, 13.
5
[Changes of vessel in steroid-induced osteonecrosis of femoral head: experimental study of rabbits].[激素性股骨头坏死中血管的变化:兔实验研究]
Zhonghua Yi Xue Za Zhi. 2006 Aug 8;86(29):2024-7.
6
[An experimental study on treatment of steroid-associated femoral head necrosis with simvastatin and BMSCs transplantation].辛伐他汀联合骨髓间充质干细胞移植治疗激素性股骨头坏死的实验研究
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2008 Mar;22(3):290-4.
7
[Experimental study on mechanism of steroid-induced avascular necrosis of femoral head].[激素性股骨头缺血性坏死机制的实验研究]
Zhonghua Wai Ke Za Zhi. 1994 Sep;32(9):515-7.
8
[An experimental study on osteocyte apoptosis in steroid-induced early osteonecrosis of femoral head].[类固醇诱导早期股骨头坏死中骨细胞凋亡的实验研究]
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2007 Mar;21(3):262-5.
9
[Experimental steroid osteonecrosis in rabbits and pathologic findings].[兔实验性类固醇性骨坏死及病理表现]
Zhonghua Wai Ke Za Zhi. 1995 Aug;33(8):485-7.
10
[MODEL ESTABLISHMENT, MRI AND PATHOLOGICAL FEATURES OF EARLY STEROID-INDUCED AVASCULAR NECROSIS OF FEMORAL HEAD IN RABBIT].[兔早期类固醇诱导的股骨头缺血性坏死的模型建立、MRI及病理特征]
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2015 Oct;29(10):1240-3.