Insulin and Glucagon Secretions, and Morphological Change of Pancreatic Islets in OLETF Rats, a Model of Type 2 Diabetes Mellitus.
10.3346/jkms.2002.17.1.34
- Author:
Eun Gyoung HONG
1
;
Hye Lim NOH
;
Seong Kyu LEE
;
Yoon Sok CHUNG
;
Kwan Woo LEE
;
Hyeon Man KIM
Author Information
1. Division of Endocrinology and Metabolism, Pochon CHA University School of Medicine, Kumi, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Rats, Inbred OLETF;
Diabetes Mellitus, Type 2;
Insulin;
Glucagon;
Islets of Langerhans;
Ultrastructure
- MeSH:
Animals;
Body Weight;
Diabetes Mellitus, Type 2/*metabolism/pathology;
Disease Models, Animal;
Glucagon/*metabolism;
Insulin/*metabolism;
Islets of Langerhans/*metabolism/pathology/ultrastructure;
Male;
Rats;
Rats, Inbred OLETF
- From:Journal of Korean Medical Science
2002;17(1):34-40
- CountryRepublic of Korea
- Language:English
-
Abstract:
This study was performed to observe the changes of glucose-related hormones and the morphological change including ultrastructure of the pancreatic islets in the male Otsuka Long-Evans Tokushima Fatty rat. Area under the curve (AUC) of glucose at the 30th (709 +/- 73 mg.h/dL) and at the 40th week (746 +/- 87 mg.h/ dL) of age were significantly higher than that at the 10th week (360 +/- 25 mg.h/ dL). AUC of insulin of the 10th week was 2.4 +/- 0.9 ng.h/mL, increased gradually to 10.8 +/- 8.3 ng.h/mL at the 30th week, and decreased to 1.8 +/- 1.2 ng.h/mL at the 40th week. The size of islet was increased at 20th week of age and the distribution of peripheral alpha cells and central beta cells at the 10th and 20th weeks was changed to a mixed pattern at the 40th week. On electron microscopic examination, beta cells at the 20th week showed many immature secretory granules, increased mitochondria, and hypertrophied Golgi complex and endoplasmic reticulum. At the 40th week, beta cell contained scanty intracellular organelles and secretory granules and apoptosis of acinar cell was observed. In conclusion, as diabetes progressed, increased secretion of insulin was accompanied by increases in size of islets and number of beta-cells in male OLETF rats showing obese type 2 diabetes. However, these compensatory changes could not overcome the requirement of insulin according to the continuous hyperglycemia after development of diabetes.
