Selectively Bred Diabetes Models: GK Rats, NSY Mice, and ON Mice

Mototsugu Nagao, Jonathan Lou S Esguerra, Anna Wendt, Akira Asai, Hitoshi Sugihara, Shinichi Oikawa, Lena Eliasson

Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

Abstract

The polygenic background of selectively bred diabetes models mimics the etiology of type 2 diabetes. So far, three different rodent models (Goto-Kakizaki rats, Nagoya-Shibata-Yasuda mice, and Oikawa-Nagao mice) have been established in the diabetes research field by continuous selective breeding for glucose tolerance from outbred rodent stocks. The origin of hyperglycemia in these rodents is mainly insulin secretion deficiency from the pancreatic β-cells and mild insulin resistance in insulin target organs. In this chapter, we summarize backgrounds and phenotypes of these rodent models to highlight their importance in diabetes research. Then, we introduce experimental methodologies to evaluate β-cell exocytosis as a putative common defect observed in these rodent models.

Original languageEnglish
Title of host publicationAnimal Models of Diabetes. Methods in Molecular Biology
EditorsA King
PublisherHumana Press
Pages25-54
Number of pages30
Volume2128
ISBN (Electronic)978-1-0716-0385-7
ISBN (Print)978-1-0716-0384-0
DOIs
Publication statusPublished - 2020 Mar 17

Publication series

NameMethods in molecular biology (Clifton, N.J.)
PublisherSpringer
ISSN (Print)1940-6029

Subject classification (UKÄ)

  • Endocrinology and Diabetes

Fingerprint

Dive into the research topics of 'Selectively Bred Diabetes Models: GK Rats, NSY Mice, and ON Mice'. Together they form a unique fingerprint.

Cite this