de Cesar Netto Cesar, Godoy-Santos Alexandre Leme, Augusto Pontin Pedro, Natalino Renato Jose Mendonça, Pereira Cesar Augusto Martins, Lima Francisco Diego de Oliveira, da Fonseca Lucas Furtado, Staggers Jackson Rucker, Cavinatto Leonardo Muntada, Schon Lew Charles, de Camargo Olavo Pires, Fernandes Túlio Diniz
Department of Orthopaedics and Traumatology, University of Sao Paulo (USP), School of Medicine, Sao Paulo, Sao Paulo, Brazil.
Department of Orthopaedics, Foot and Ankle Surgery, Medstar Union Memorial Hospital, Baltimore, Maryland, United States of America.
PLoS One. 2018 Feb 13;13(2):e0192769. doi: 10.1371/journal.pone.0192769. eCollection 2018.
Our goal was to develop a novel technique for inducing Achilles tendinopathy in animal models which more accurately represents the progressive histological and biomechanical characteristic of chronic Achilles tendinopathy in humans. In this animal research study, forty-five rabbits were randomly assigned to three groups and given bilateral Achilles injections. Low dose (LD group) (n = 18) underwent a novel technique with three low-dose (0.1mg) injections of collagenase that were separated by two weeks, the high dose group (HD) (n = 18) underwent traditional single high-dose (0.3mg) injections, and the third group were controls (n = 9). Six rabbits were sacrificed from each experimental group (LD and HD) at 10, 12 and 16 weeks. Control animals were sacrificed after 16 weeks. Histological and biomechanical properties were then compared in all three groups. At 10 weeks, Bonar score and tendon cross sectional area was highest in HD group, with impaired biomechanical properties compared to LD group. At 12 weeks, Bonar score was higher in LD group, with similar biomechanical findings when compared to HD group. After 16 weeks, Bonar score was significantly increased for both LD group (11,8±2,28) and HD group (5,6±2,51), when compared to controls (2±0,76). LD group showed more pronounced histological and biomechanical findings, including cross sectional area of the tendon, Young's modulus, yield stress and ultimate tensile strength. In conclusion, Achilles tendinopathy in animal models that were induced by serial injections of low-dose collagenase showed more pronounced histological and biomechanical findings after 16 weeks than traditional techniques, mimicking better the progressive and chronic characteristic of the tendinopathy in humans.
我们的目标是开发一种在动物模型中诱导跟腱病的新技术,该技术能更准确地呈现人类慢性跟腱病的渐进性组织学和生物力学特征。在这项动物研究中,45只兔子被随机分为三组并接受双侧跟腱注射。低剂量组(LD组)(n = 18)采用一种新技术,分三次低剂量(0.1mg)注射胶原酶,每次注射间隔两周;高剂量组(HD组)(n = 18)接受传统的单次高剂量(0.3mg)注射;第三组为对照组(n = 9)。每组实验兔(LD组和HD组)分别在第10、12和16周处死6只兔子。对照组兔子在16周后处死。然后比较三组的组织学和生物力学特性。在第10周时,HD组的博纳尔评分和肌腱横截面积最高,但与LD组相比生物力学性能受损。在第12周时,LD组的博纳尔评分更高,与HD组相比生物力学结果相似。16周后,与对照组(2±0.76)相比,LD组(11.8±2.28)和HD组(5.6±2.51)的博纳尔评分均显著增加。LD组在组织学和生物力学方面表现出更明显的变化,包括肌腱横截面积、杨氏模量、屈服应力和极限抗拉强度。总之,与传统技术相比,连续注射低剂量胶原酶诱导的动物模型跟腱病在16周后在组织学和生物力学方面表现出更明显的变化,能更好地模拟人类跟腱病的渐进性和慢性特征。