• 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

仙灵骨葆对大鼠前交叉韧带横断模型关节软骨退变的抑制作用

[Effect of xianlinggubao in suppressing articular cartilage degeneration of anterior cruciate ligament transection model in rats].

作者信息

Li Qiang, Zhang Liu, Li Zhen, Mu Shulin, Cheng Tan, Tian Faming, Liu Yongqiang

机构信息

Department of Orthopaedics, Affiliated Hospital of North China Coal Medical College, Tangshan Hebei, 063000, PR China.

出版信息

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2009 Mar;23(3):294-8.

PMID:19366137
Abstract

OBJECTIVE

To investigate the effects of xianlinggubao (XLGB) on subchondral bone and articular cartilage in the rat osteoarthritis model induced by anterior cruciate ligament transection (ACLT).

METHODS

Twenty-four 3-month-old female SD rats were divided randomly into 3 groups (n=8): Sham group (group A), ACLT group (group B) and XLGB group (group C). The osteoarthritis model was made by ACLT in groups B and C, the joint cave was sutured after exposure of ACL in group A. After 4 days, XLGB was given at 250 mg/(kgd) in group C and the equivalent amount of saline was given in groups A and B. After 12 weeks, the gross appearance of femoral condyles was observed, the degree of cartilage degeneration was scored by Mankin scoring system. The immunostaining for MMP-13 was performed to investigate the effect of XLGB on prevention of cartilage matrix loss. The bone mineral density (BMD) measurement and bone histomorphometric analysis were done in subchondral bone of right distal femur and proximal tibia after 12 weeks.

RESULTS

The gross appearance of femoral condyles showed that ulcer in the group C was smaller than that in group B after 12 weeks. The Mankin's scale and IA value for MMP-13 in group C were markedly lower than those in group B (P < 0.05). BMD of the subchondral bone in the group B was significantly lower than those in the groups A and C (P < 0.05). The bone mass in group C were significantly higher than that in group B (P < 0.05).

CONCLUSION

Oral administration of XLGB (250 mg/kg per day) for 12 weeks could prevent the cartilage degeneration of rats after ACLT, down-regulating MMP-13 and increasing subchondral bone mass might participate in this process.

摘要

目的

探讨仙灵骨葆(XLGB)对前交叉韧带横断(ACLT)诱导的大鼠骨关节炎模型软骨下骨和关节软骨的影响。

方法

将24只3月龄雌性SD大鼠随机分为3组(n = 8):假手术组(A组)、ACLT组(B组)和仙灵骨葆组(C组)。B组和C组通过ACLT制备骨关节炎模型,A组暴露前交叉韧带后缝合关节腔。4天后,C组给予仙灵骨葆250 mg/(kg·d),A组和B组给予等量生理盐水。12周后,观察股骨髁大体形态,采用Mankin评分系统对软骨退变程度进行评分。进行基质金属蛋白酶-13(MMP-13)免疫染色,以研究仙灵骨葆对预防软骨基质丢失的作用。12周后对右股骨远端和胫骨近端软骨下骨进行骨密度(BMD)测量和骨组织形态计量分析。

结果

股骨髁大体形态显示,12周后C组溃疡小于B组。C组Mankin评分和MMP-13免疫活性值均明显低于B组(P < 0.05)。B组软骨下骨BMD明显低于A组和C组(P < 0.05)。C组骨量明显高于B组(P < 0.05)。

结论

口服仙灵骨葆(250 mg/kg每日)12周可预防ACLT后大鼠软骨退变,下调MMP-13和增加软骨下骨量可能参与此过程。

相似文献

1
[Effect of xianlinggubao in suppressing articular cartilage degeneration of anterior cruciate ligament transection model in rats].仙灵骨葆对大鼠前交叉韧带横断模型关节软骨退变的抑制作用
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2009 Mar;23(3):294-8.
2
[In vitro effect of alendronate on chondrocytes and articular cartilage and subchondral bone in rabbit anterior cruciate ligament transection model].阿仑膦酸钠对兔前交叉韧带横断模型中软骨细胞、关节软骨及软骨下骨的体外作用
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2009 Dec;23(12):1474-81.
3
Joint distraction attenuates osteoarthritis by reducing secondary inflammation, cartilage degeneration and subchondral bone aberrant change.关节牵张通过减轻继发性炎症、软骨退变和软骨下骨异常改变来减轻骨关节炎。
Osteoarthritis Cartilage. 2015 Oct;23(10):1728-35. doi: 10.1016/j.joca.2015.05.018. Epub 2015 May 29.
4
Low magnitude high frequency vibration accelerated cartilage degeneration but improved epiphyseal bone formation in anterior cruciate ligament transect induced osteoarthritis rat model.低强度高频振动加速了前交叉韧带横断诱导的骨关节炎大鼠模型中的软骨退变,但改善了骨骺骨形成。
Osteoarthritis Cartilage. 2014 Jul;22(7):1061-7. doi: 10.1016/j.joca.2014.05.004. Epub 2014 May 20.
5
The role of subchondral bone remodeling in osteoarthritis: reduction of cartilage degeneration and prevention of osteophyte formation by alendronate in the rat anterior cruciate ligament transection model.软骨下骨重塑在骨关节炎中的作用:阿仑膦酸盐在大鼠前交叉韧带横断模型中减少软骨退变及预防骨赘形成
Arthritis Rheum. 2004 Apr;50(4):1193-206. doi: 10.1002/art.20124.
6
Alterations in subchondral bone plate, trabecular bone and articular cartilage properties of rabbit femoral condyles at 4 weeks after anterior cruciate ligament transection.前交叉韧带横断术后4周兔股骨髁软骨下骨板、松质骨及关节软骨特性的改变
Osteoarthritis Cartilage. 2015 Mar;23(3):414-22. doi: 10.1016/j.joca.2014.11.023. Epub 2014 Dec 3.
7
Extracorporeal shockwave therapy shows site-specific effects in osteoarthritis of the knee in rats.体外冲击波疗法在大鼠膝关节骨关节炎中显示出特定部位的疗效。
J Surg Res. 2013 Aug;183(2):612-9. doi: 10.1016/j.jss.2013.02.006. Epub 2013 Feb 26.
8
Quantitative MR T2 measurement of articular cartilage to assess the treatment effect of intra-articular hyaluronic acid injection on experimental osteoarthritis induced by ACLX.定量磁共振 T2 测量关节软骨评估关节内透明质酸注射治疗 ACLX 诱导的实验性骨关节炎的疗效。
Osteoarthritis Cartilage. 2010 Jan;18(1):54-60. doi: 10.1016/j.joca.2009.08.014. Epub 2009 Sep 6.
9
Protective effects of tumor necrosis factor-α blockade by adalimumab on articular cartilage and subchondral bone in a rat model of osteoarthritis.阿达木单抗阻断肿瘤坏死因子-α对骨关节炎大鼠模型关节软骨和软骨下骨的保护作用。
Braz J Med Biol Res. 2015 Oct;48(10):863-70. doi: 10.1590/1414-431X20154407. Epub 2015 Jul 31.
10
[Effect of extracorporeal shock wave therapy on cartilage and subchondral bone remodeling in rabbits with ACLT-induced osteoarthritis].[体外冲击波疗法对前交叉韧带切断术诱导的兔骨关节炎软骨及软骨下骨重塑的影响]
Sichuan Da Xue Xue Bao Yi Xue Ban. 2014 Jan;45(1):120-5.

引用本文的文献

1
Application of Microsponge Drug Platform to Enhance Methotrexate Administration in Rheumatoid Arthritis Therapy.微球药物平台在类风湿关节炎治疗中增强甲氨蝶呤给药的应用。
Pharmaceutics. 2024 Dec 13;16(12):1593. doi: 10.3390/pharmaceutics16121593.