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使用雄性和雌性小鼠胫骨机械位移造成的 ACL 中部完全和部分撕裂。

Full and Partial Mid-substance ACL Rupture Using Mechanical Tibial Displacement in Male and Female Mice.

机构信息

Department of Microbiology, Immunology, and Pathology, Colorado State University, 1682 Campus Delivery, Fort Collins, CO, 80523-1621, USA.

Department of Clinical Sciences, Colorado State University, Fort Collins, CO, 80523, USA.

出版信息

Ann Biomed Eng. 2023 Mar;51(3):579-593. doi: 10.1007/s10439-022-03065-1. Epub 2022 Sep 7.

Abstract

The anterior cruciate ligament (ACL) is the most commonly injured knee ligament. Surgical reconstruction is the gold standard treatment for ACL ruptures, but 20-50% of patients develop post-traumatic osteoarthritis (PTOA). ACL rupture is thus a well-recognized etiology of PTOA; however, little is known about the initial relationship between ligamentous injury and subsequent PTOA. The goals of this project were to: (1) develop both partial and full models of mid-substance ACL rupture in male and female mice using non-invasive mechanical methods by means of tibial displacement; and (2) to characterize early PTOA changes in the full ACL rupture model. A custom material testing system was utilized to induce either partial or full ACL rupture by means of tibial displacement at 1.6 or 2.0 mm, respectively. Mice were euthanized either (i) immediately post-injury to determine rupture success rates or (ii) 14 days post-injury to evaluate early PTOA progression following full ACL rupture. Our models demonstrated high efficacy in inciting either full or partial ACL rupture in male and female mice within the mid-substance of the ACL. These tools can be utilized for preclinical testing of potential therapeutics and to further our understanding of PTOA following ACL rupture.

摘要

前交叉韧带(ACL)是最常见的膝关节韧带损伤。手术重建是 ACL 断裂的金标准治疗方法,但 20-50%的患者会发展为创伤后骨关节炎(PTOA)。因此,ACL 断裂是 PTOA 的一个公认病因;然而,对于韧带损伤与随后的 PTOA 之间的初始关系知之甚少。本项目的目标是:(1)通过胫骨位移的非侵入性机械方法,在雄性和雌性小鼠中分别建立部分和完全 ACL 中段撕裂模型;(2)在完全 ACL 撕裂模型中,对早期 PTOA 变化进行特征描述。使用定制的材料测试系统,通过胫骨位移分别以 1.6 或 2.0 毫米的幅度诱导部分或完全 ACL 撕裂。在损伤后立即(i)处死小鼠以确定撕裂成功率,或(ii)在完全 ACL 撕裂后 14 天处死小鼠以评估早期 PTOA 进展。我们的模型在雄性和雌性小鼠的 ACL 中段成功地高效诱发了完全或部分 ACL 撕裂。这些工具可用于临床前测试潜在治疗方法,并进一步了解 ACL 撕裂后的 PTOA。

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