Rolandsson O, Haney M F, Hagg E, Biber B, Lernmark A
Family Medicine, Department of Public Health and Clinical Medicine, Umeå University, S-90185 Umeå, Sweden.
Autoimmunity. 2002 Jul;35(4):261-4. doi: 10.1080/0891693021000010703.
Studies on the pathogenic process in type 1 diabetes are often performed in animal models. Low-dose administration of streptozotocin has been used to induce diabetes with pathological alterations similar to human type 1 diabetes in the animals. Rodent models are frequently used but there is a need of developing new models including larger animals. In this study we wanted to investigate to what extent a minipig was sensitive to low-dose streptozotocin for induction of diabetes with features of human Type I diabetes. A female Göttingen minipig received two low-doses (40 mg/kg) of streptozotocin with an 11-day interval. Serum was analysed for the presence of the enzyme glutamic acid decarboxylase, isoform 65, (GAD65) and autoantibodies against glutamic acid decarboxylase, isoform 65 (GAD65A), isoform 67 (GAD67A), insulinoma antigen 2 (IA-2) and insulin (IAA). Pancreas tissue was fixated in formaldehyde and was sent for pathoanatomical examination. The minipig became hyperglycaemic after the second injection of streptozotocin. The pathoanatomical examination showed atrophy of the beta-cell population, depletion of insulin with preserved glucagon content. There was no sign of insulitis. Both GAD65 and GAD65A were detected while GAD67A and IAA were absent. It is concluded that chronic diabetes developed after low-dose streptozotocin injection in a female minipig with the characteristics of the end stage of type 1 diabetes. This pilot study suggests that minipigs show promise as a model to induce diabetes by injections of low-dose streptozotocin.
1型糖尿病致病过程的研究通常在动物模型中进行。低剂量注射链脲佐菌素已被用于在动物中诱导出具有类似于人类1型糖尿病病理改变的糖尿病。啮齿动物模型经常被使用,但需要开发包括大型动物在内的新模型。在本研究中,我们想探究小型猪对低剂量链脲佐菌素诱导具有人类1型糖尿病特征的糖尿病的敏感程度。一只雌性哥廷根小型猪间隔11天接受了两次低剂量(40mg/kg)的链脲佐菌素注射。分析血清中是否存在谷氨酸脱羧酶65型(GAD65)以及针对谷氨酸脱羧酶65型(GAD65A)、67型(GAD67A)、胰岛瘤抗原2(IA-2)和胰岛素(IAA)的自身抗体。胰腺组织用甲醛固定并送去进行病理解剖检查。在第二次注射链脲佐菌素后,小型猪出现高血糖。病理解剖检查显示β细胞群萎缩,胰岛素减少而胰高血糖素含量保留。没有胰岛炎的迹象。检测到了GAD65和GAD65A,而未检测到GAD67A和IAA。结论是,雌性小型猪在低剂量注射链脲佐菌素后发展为慢性糖尿病,具有1型糖尿病终末期的特征。这项初步研究表明,小型猪有望成为通过注射低剂量链脲佐菌素诱导糖尿病的模型。