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Acute molecular biological responses during spontaneous anterior cruciate ligament healing in a rat model

机译:在大鼠模型中自发前部十字韧带愈合期间的急性分子生物反应

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Background Anterior cruciate ligament (ACL) injury is one of the most common injuries of the knee joint and is becoming more prevalent. While ACL reconstruction is considered the "gold standard" of treatment, some studies have demonstrated natural spontaneous healing of the ACL in humans, rabbits, and rats. At this time, the mechanism of ACL healing is poorly understood. Aims The purpose of this study was to determine the process of ACL healing by examining the molecular and histological changes in the acute phases, using an ACL-Transection model and a spontaneous ACL healing model. Methods Sixty adult male Wistar rats were randomly assigned to two groups: the ACL transection (ACLT) group and the controlled abnormal movement (CAM) group. Thirty rats were randomly assigned to three groups (day 1, day 3, and day 5). Then, all rats underwent an ACL transection procedure. The CAM group rats underwent controlled abnormal extra-articular tibial translation. Samples were harvested from rats and used for histological and biochemical analyses. Results Both, the ACLT and the CAM groups exhibited ruptured ACLs. However, in the CAM group, the ends of the proximal remnants were not retracted. Expressions of MMP-3 and PDGF-a increased, and expression of TGF-β1 decreased in the CAM group on day 5 (p<0.01); PDGF-p expression in the CAM group increased significantly at each time point (p< 0.01). Conclusion Our results suggested that controlling abnormal movements changed intra-articular responses positively during the acute phase both histologically and biochemically.
机译:背景技术前令人毛病(ACL)损伤是膝关节最常见的伤害之一,并且变得越来越普遍。虽然ACL重建被认为是“黄金标准”的治疗,但一些研究表明了人类,兔和大鼠ACL的自然自发愈合。此时,ACL愈合的机制很差理解。目的,本研究的目的是通过检查急性相中的分子和组织学变化,使用ACL-横转矩模型和自发ACL愈合模型来确定ACL愈合的方法。方法将60只成年雄性Wistar大鼠随机分配给两组:AC1横敏(ACLT)组和受控异常运动(CAM)组。将30只大鼠随机分配到三组(第1天,第3天和第5天)。然后,所有大鼠都经历了ACL转化过程。凸轮组大鼠接受了受控异常关节胫骨翻译。从大鼠收获样品并用于组织学和生物化学分析。结果两者,ACLT和凸轮组表现出破裂的ACL。然而,在凸轮组中,近端残余物的末端没有缩回。 MMP-3和PDGF-A的表达增加,第5天在凸轮组中降低TGF-β1的表达(P <0.01);凸轮组中的PDGF-P表达在每个时间点显着增加(P <0.01)。结论我们的研究结果表明,控制异常运动在组织学和生物化学上的急性相期间,在急性相期间呈上变化。

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