Selectively Bred Diabetes Models: GK Rats, NSY Mice, and ON Mice.
Animals
Diabetes Mellitus, Experimental
/ etiology
Diabetes Mellitus, Type 1
/ etiology
Diabetes Mellitus, Type 2
/ etiology
Exocytosis
Gene Expression Profiling
/ methods
Glucose Intolerance
Insulin Resistance
/ physiology
Insulin Secretion
/ physiology
Insulin-Secreting Cells
/ chemistry
Mice
Mice, Inbred C3H
Patch-Clamp Techniques
/ methods
Phenotype
Rats
Rats, Wistar
Selective Breeding
/ genetics
Capacitance measurement
Exocytosis
Goto-Kakizaki rats
Insulin secretion
Islets
Nagoya-Shibata-Yasuda mice
Oikawa-Nagao mice
β-Cells
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2020
2020
Historique:
entrez:
18
3
2020
pubmed:
18
3
2020
medline:
11
3
2021
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 32180184
doi: 10.1007/978-1-0716-0385-7_3
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM