Toritsuka Y, Shino K, Horibe S, Nakamura N, Matsumoto N, Ochi T
Department of Orthopaedic Surgery, Osaka University Medical School, Suita, Japan.
J Orthop Res. 1997 Mar;15(2):294-300. doi: 10.1002/jor.1100150220.
Freezing or freeze-drying and gamma-irradiation are techniques currently used for processing tendon allografts. However, it is still unknown how these processing methods affect graft remodeling. In this study, we used a rat patellar tendon transplantation model to investigate the effect of various processing methods on remodeling by quantifying loss of collagen labeled with a radioactive isotope. The grafts were divided into the following four groups according to the processing method: fresh-frozen, freeze-dried, fresh-frozen and gamma-irradiated, or freeze-dried and gamma-irradiated. The percentage of donor collagen, calculated from hydroxyproline content and radioactivity level, was used as an indicator of graft remodeling. At 2 weeks, the level of donor collagen in the fresh-frozen group was 62%; in the freeze-dried group, 59%; in the fresh-frozen and irradiated group, 57%; and in the freeze-dried and irradiated group, 44%. At 4 weeks, the percentage of donor collagen remaining in grafts decreased to 38% in the fresh-frozen group, 19% in the freeze-dried group, 27% in the fresh-frozen and irradiated group, and 12% in the freeze-dried and irradiated group. Finally, at 12 weeks, the levels were 19% in the fresh-frozen group, 20% in the freeze-dried group, 15% in the fresh-frozen and irradiated group, and 6% in the freeze-dried and irradiated group. The percentages of donor collagen in the freeze-dried and the fresh-frozen and irradiated groups were significantly lower than that in the fresh-frozen group at 4 weeks. The values for the freeze-dried and irradiated group were significantly lower than those for the fresh-frozen and irradiated group at 4 and 12 weeks. These data suggest that freeze-drying, freeze-drying followed by gamma-irradiation, and fresh-freezing followed by gamma-irradiation temporarily accelerate graft remodeling.
冷冻或冻干以及伽马射线辐照是目前用于处理同种异体肌腱的技术。然而,这些处理方法如何影响移植物重塑仍不清楚。在本研究中,我们使用大鼠髌腱移植模型,通过量化放射性同位素标记的胶原蛋白损失来研究各种处理方法对重塑的影响。根据处理方法,移植物被分为以下四组:新鲜冷冻组、冻干组、新鲜冷冻并伽马射线辐照组、或冻干并伽马射线辐照组。由羟脯氨酸含量和放射性水平计算得出的供体胶原蛋白百分比,被用作移植物重塑的指标。在2周时,新鲜冷冻组的供体胶原蛋白水平为62%;冻干组为59%;新鲜冷冻并辐照组为57%;冻干并辐照组为44%。在4周时,新鲜冷冻组移植物中剩余的供体胶原蛋白百分比降至38%,冻干组为19%,新鲜冷冻并辐照组为27%,冻干并辐照组为12%。最后,在12周时,新鲜冷冻组的水平为19%,冻干组为20%,新鲜冷冻并辐照组为15%,冻干并辐照组为6%。在4周时,冻干组以及新鲜冷冻并辐照组的供体胶原蛋白百分比显著低于新鲜冷冻组。在4周和12周时,冻干并辐照组的值显著低于新鲜冷冻并辐照组。这些数据表明,冻干、冻干后伽马射线辐照以及新鲜冷冻后伽马射线辐照会暂时加速移植物重塑。