首页> 美国卫生研究院文献>Brazilian Journal of Medical and Biological Research >Protective effects of tumor necrosis factor-α blockade by adalimumab onarticular cartilage and subchondral bone in a rat model ofosteoarthritis
【2h】

Protective effects of tumor necrosis factor-α blockade by adalimumab onarticular cartilage and subchondral bone in a rat model ofosteoarthritis

机译:阿达木单抗阻断肿瘤坏死因子-α的保护作用大鼠关节炎模型的关节软骨和软骨下骨。骨关节炎

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We aimed to investigate the effects of an anti-tumor necrosis factor-α antibody (ATNF) on cartilage and subchondral bone in a rat model of osteoarthritis. Twenty-four rats were randomly divided into three groups: sham-operated group (n=8); anterior cruciate ligament transection (ACLT)+normal saline (NS) group (n=8); and ACLT+ATNF group (n=8). The rats in the ACLT+ATNF group received subcutaneous injections of ATNF (20 μg/kg) for 12 weeks, while those in the ACLT+NS group received NS at the same dose for 12 weeks. All rats were euthanized at 12 weeks after surgery and specimens from the affected knees were harvested. Hematoxylin and eosin staining, Masson's trichrome staining, and Mankin score assessment were carried out to evaluate the cartilage status and cartilage matrix degradation. Matrix metalloproteinase (MMP)-13 immunohistochemistry was performed to assess the cartilage molecular metabolism. Bone histomorphometry was used to observe the subchondral trabecular microstructure. Compared with the rats in the ACLT+NS group, histological and Mankin score analyses showed that ATNF treatment reduced the severity of the cartilage lesions and led to a lower Mankin score. Immunohistochemical and histomorphometric analyses revealed that ATNF treatment reduced the ACLT-induced destruction of the subchondral trabecular microstructure, and decreased MMP-13 expression. ATNFtreatment may delay degradation of the extracellular matrix via a decrease in MMP-13expression. ATNF treatment probably protects articular cartilage by improving thestructure of the subchondral bone and reducing the degradation of the cartilagematrix.
机译:我们旨在研究骨关节炎大鼠模型中抗肿瘤坏死因子-α抗体(ATNF)对软骨和软骨下骨的影响。 24只大鼠随机分为三组:假手术组(n = 8);假手术组(n = 8)。前十字韧带横断(ACLT)+生理盐水(NS)组(n = 8); ACLT + ATNF组(n = 8)。 ACLT + ATNF组的大鼠皮下注射ATNF(20μg/ kg),持续12周,而ACLT + NS组的大鼠以相同剂量接受NS,持续12周。在手术后第12周对所有大鼠实施安乐死,并从患膝中收集标本。进行苏木精和曙红染色,Masson三色染色和Mankin评分评估以评估软骨状态和软骨基质降解。进行基质金属蛋白酶(MMP)-13免疫组化评估软骨分子代谢。骨组织形态学用于观察软骨下小梁的微结构。与ACLT + NS组的大鼠相比,组织学和Mankin评分分析表明,ATNF治疗可减轻软骨病变的严重程度,并降低Mankin评分。免疫组织化学和组织形态学分析显示,ATNF处理减少了ACLT诱导的软骨下小梁下微结构的破坏,并降低了MMP-13的表达。坏死因子治疗可能会通过降低MMP-13延迟细胞外基质的降解表达。 ATNF治疗可能通过改善ATNF来保护关节软骨软骨下骨的结构并减少软骨的退化矩阵。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号