Hagenah M, Simon B, Böhnke M
Universitäts-Augenklinik, Hamburg, BRD.
Ophthalmic Res. 1993;25(4):210-5. doi: 10.1159/000267315.
Clinical and experimental studies with rabbit and human corneas have shown the correlation between short postmortem times and successful corneal cryopreservation. In this experimental study we investigated this phenomenon considering the latent freeze-thaw-induced cell damage. Enucleated eye-balls of freshly slaughtered pigs were stored in moist chambers at 4 degrees C for 2, 4, 8, 16, 32, and 72 h before cryopreservation. After thawing, the corneas were organ-cultured for 1 day. After staining with trypan blue and alizarin red S the tissue was evaluated morphometrically, calculating the amount of necrotic areas on the central corneal surface and the endothelial cell density. Corneas stored up to 32 h before cryopreservation showed no difference regarding the amount of necrosis and endothelial cell density compared to freshly cryopreserved tissue. Corneas stored 72 h before cryopreservation revealed no endothelial cell survival. We conclude that a post-mortem time of up to 32 h before corneal cryopreservation has no influence on endothelial cell survival.
对兔和人角膜进行的临床及实验研究表明,死后时间短与角膜冷冻保存成功之间存在关联。在本实验研究中,我们考虑潜在的冻融诱导细胞损伤来研究这一现象。将刚宰杀的猪摘除的眼球在4℃的潮湿环境中保存2、4、8、16、32和72小时后进行冷冻保存。解冻后,将角膜进行器官培养1天。用台盼蓝和茜素红S染色后,对组织进行形态计量学评估,计算角膜中央表面坏死区域的数量和内皮细胞密度。与新鲜冷冻保存的组织相比,冷冻保存前保存长达32小时的角膜在坏死数量和内皮细胞密度方面没有差异。冷冻保存前保存72小时的角膜未显示内皮细胞存活。我们得出结论,角膜冷冻保存前长达32小时的死后时间对内皮细胞存活没有影响。