Taylor M J, Duffy T J, Hunt C J, Morgan S R, Davisson P J
Cryobiology. 1983 Apr;20(2):185-204. doi: 10.1016/0011-2240(83)90007-x.
The cryoprotectants dimethyl sulfoxide (Me2SO) and glycerol have been used for the cryopreservation of fetal rat pancreases but only Me2SO has been reported for the cryopreservation of adult rat islets. Since glycerol may be preferred to Me2SO for clinical use, this study was undertaken to compare the effectiveness of these cryoprotectants during the slow cooling of isolated adult rat islets. Islets of Langerhans prepared from the pancreases of WAG rats by collagenase digestion were stored at -196 degrees C after slow cooling (0.3 degrees C/min) to -70 degrees C in the presence of multimolar concentrations of either Me2SO or glycerol. Samples were rewarmed slowly (approximately 10 degrees C/min) and dilution of the cryoprotectant was achieved using medium containing sucrose. Function was assessed by determination of the time course of the glucose-induced insulin release during in vitro perifusion at 37 degrees C and also by isograft transplantation. Transplants were carried out by intraportal injection of a minimum of 1700 frozen and thawed islets into streptozotocin-induced diabetic recipients and tissue function was assessed by monitoring blood glucose levels and body weight changes. Without exception the islets frozen and thawed in the presence of glycerol failed to reduce high serum glucose levels of recipient rats and in vitro dynamic release curves showed to demonstrate a glucose-sensitive insulin release pattern. Reversal of the diabetic conditions was achieved in two of five animals receiving islets which had been frozen and thawed with 2 M Me2SO; and in one of three animals receiving islets cryopreserved with 3 M Me2SO. Nevertheless, perifusion studies showed that the pattern of insulin secretion from groups of cryopreserved islets which did show an ability to secrete insulin was atypical compared with that of untreated controls, suggesting that the tissue was altered or damaged in some way.
冷冻保护剂二甲基亚砜(Me2SO)和甘油已用于胎鼠胰腺的冷冻保存,但仅有二甲基亚砜用于成年大鼠胰岛的冷冻保存的报道。由于在临床应用中甘油可能比二甲基亚砜更受青睐,因此进行本研究以比较这些冷冻保护剂在成年大鼠分离胰岛缓慢冷却过程中的效果。通过胶原酶消化从WAG大鼠胰腺制备的胰岛,在多摩尔浓度的二甲基亚砜或甘油存在下缓慢冷却(0.3℃/分钟)至-70℃后,于-196℃保存。样品缓慢复温(约10℃/分钟),并使用含蔗糖的培养基实现冷冻保护剂的稀释。通过在37℃体外灌流期间测定葡萄糖诱导的胰岛素释放的时间进程以及通过同基因移植来评估功能。通过将至少1700个冻融胰岛经门静脉注射到链脲佐菌素诱导的糖尿病受体中进行移植,并通过监测血糖水平和体重变化来评估组织功能。无一例外,在甘油存在下冻融的胰岛未能降低受体大鼠的高血糖水平,并且体外动态释放曲线显示未呈现葡萄糖敏感性胰岛素释放模式。在接受用2M二甲基亚砜冻融的胰岛的五只动物中有两只实现了糖尿病状态的逆转;在接受用3M二甲基亚砜冷冻保存的胰岛的三只动物中有一只实现了逆转。然而,灌流研究表明,与未处理的对照相比,确实显示出胰岛素分泌能力的冷冻保存胰岛组的胰岛素分泌模式不典型,这表明组织在某种程度上发生了改变或损伤。