Chronological characterization of diabetes development in male Spontaneously Diabetic Torii rats

被引:102
作者
Masuyama, T
Komeda, K
Hara, A
Noda, M
Shinohara, M
Oikawa, T
Kanazawa, Y
Taniguchi, K
机构
[1] Jichi Med Sch, Minami Kawachi, Tochigi 3290498, Japan
[2] Asahi Life Fdn, Inst Diabet Care & Res, Chiyoda Ku, Tokyo 1000005, Japan
[3] Tokyo Med Univ, Anim Res Ctr, Div Lab Anim Sci, Shinjuku Ku, Tokyo 1608402, Japan
[4] Iwate Univ, Fac Agr, Dept Vet Anat, Morioka, Iwate 0208550, Japan
[5] Torii Pharmaceut Co Ltd, Chuo Ku, Tokyo 1038439, Japan
关键词
beta-cell; diabetes; fibrosis; glucose intolerance; hyperglycemia; hypoinsulinemia; microvascular event; nonobese; pancreatic islet;
D O I
10.1016/j.bbrc.2003.12.180
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
To characterize the underlying mechanisms of diabetes development in males of the Spontaneously Diabetic Torii (SDT) rat, a novel spontaneous model for diabetes, we chronologically examined them, focusing on their diabetic features and the pathological changes in the pancreatic islets. Male SDT rats exhibited glucose intolerance with impaired insulin secretion after 14 weeks and developed diabetes with remarkable hyperglycemia and marked hypoinsulinemia after 20 weeks. At prediabetic stage (10-20 weeks), they were normoglycemic, but had significantly lower insulin levels of plasma and pancreas than the normal rats. Their beta-cell volume was already smaller significantly at 10 weeks than that of normal rats. The primary changes of the pancreatic islets were microvascular events such as congestion and hemorrhage at 8-10 weeks. Thereafter, the SDT rat islets were affected with inflammation and progressive fibrosis (at 10 20 weeks), and eventually atrophied with a loss of beta-cells (at 38 weeks). These results indicate that the male SDT rats develop spontaneous diabetes with an absolute decrease in the insulin secretory capacity of the islets. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:870 / 877
页数:8
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