Laboratory of Veterinary Physiology, School of Veterinary Medicine, Faculty of Veterinary Science, Nippon Veterinary and Life Science University, Tokyo 180-8602, Japan.
J Diabetes Res. 2019 Jul 31;2019:8153140. doi: 10.1155/2019/8153140. eCollection 2019.
A variety of animal models of diabetes mellitus (DM) are required to study the genetics and pathophysiology of DM. We established a novel rat strain showing nonobese type 2 diabetes with enlarged kidneys from the LEA.PET- congenic strain and named it Diabetes with Enlarged Kidney (DEK). The body growth of DEK affected rats was similar to that of normal rats before the development of DM but was attenuated with the deterioration of DM. There was a marked difference in the etiology of DEK by gender: DM phenotypes including polyuria, polydipsia, and hyperglycemia (nonfasting blood glucose over 300 mg/dl) were found in male rats aged over 10 weeks but not in female rats. The cumulative incidence of DM in DEK males at the age of 30 weeks was 44.8%. Oral glucose tolerance tests showed glucose intolerance and decreased insulin secretion in response to glucose loading in affected males, features which were exacerbated with age. Affected males exhibited disorganized architecture of pancreatic islets, decreased numbers of cells, and markedly decreased expression of insulin, despite no pathological findings of hemorrhage or infiltration of inflammatory cells in the pancreatic islet. Age-related islet fibrosis appeared similar in normal and affected males. Affected males also showed enlarged kidneys with dilation of renal tubules in both the cortex and medulla, but no obvious glomerular lesions typical of diabetic nephropathy (DN) at the age of 30 weeks. Plasma levels of urea nitrogen and creatinine were normal, but hypoalbuminemia was detected. These pathophysiological features in affected males indicated that their renal function was almost maintained despite severe DM. Taken together, these findings indicate that the affected males of the DEK strain are a novel nonobese type 2 diabetes rat model useful for studying the mechanisms underlying cell loss and identifying genetic factors protective against DN.
需要各种糖尿病(DM)动物模型来研究 DM 的遗传学和病理生理学。我们从 LEA.PET 近交系建立了一种新型大鼠品系,该品系表现出非肥胖型 2 型糖尿病伴肾脏增大,并将其命名为糖尿病伴肾脏增大(DEK)。DEK 受影响大鼠的体重增长在 DM 发展前与正常大鼠相似,但随着 DM 的恶化而减弱。DEK 按性别在病因上存在明显差异:10 周龄以上雄性大鼠出现多尿、多饮和高血糖(非空腹血糖超过 300mg/dl)等 DM 表型,但雌性大鼠没有。30 周龄时,DEK 雄性大鼠的 DM 累积发病率为 44.8%。口服葡萄糖耐量试验显示,受影响雄性的葡萄糖耐量和胰岛素分泌减少,随着年龄的增长,这些特征加剧。受影响雄性的胰岛结构紊乱,β细胞数量减少,胰岛素表达明显减少,但胰岛内没有出血或炎症细胞浸润等病理发现。正常和受影响雄性的年龄相关胰岛纤维化表现相似。受影响雄性还表现出肾脏增大,皮质和髓质的肾小管扩张,但在 30 周龄时没有典型的糖尿病肾病(DN)肾小球病变。血尿素氮和肌酐水平正常,但白蛋白降低。受影响雄性的这些病理生理特征表明,尽管患有严重的 DM,但它们的肾功能几乎得到维持。综上所述,这些发现表明,DEK 系受影响雄性大鼠是一种新型的非肥胖 2 型糖尿病大鼠模型,可用于研究β细胞丧失的机制,并确定对 DN 有保护作用的遗传因素。