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


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
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

Pagination

25-54

Auteurs

Mototsugu Nagao (M)

Islet Cell Exocytosis, Lund University Diabetes Centre, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden. s8067@nms.ac.jp.
Clinical Research Centre, Skåne University Hospital, Lund and Malmö, Sweden. s8067@nms.ac.jp.
Department of Endocrinology, Diabetes and Metabolism, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan. s8067@nms.ac.jp.

Jonathan Lou S Esguerra (JLS)

Islet Cell Exocytosis, Lund University Diabetes Centre, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Clinical Research Centre, Skåne University Hospital, Lund and Malmö, Sweden.

Anna Wendt (A)

Islet Cell Exocytosis, Lund University Diabetes Centre, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Clinical Research Centre, Skåne University Hospital, Lund and Malmö, Sweden.

Akira Asai (A)

Department of Endocrinology, Diabetes and Metabolism, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Food and Health Science Research Unit, Graduate School of Agricultural Science, Tohoku University, Sendai, Japan.

Hitoshi Sugihara (H)

Department of Endocrinology, Diabetes and Metabolism, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.

Shinichi Oikawa (S)

Department of Endocrinology, Diabetes and Metabolism, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Diabetes and Lifestyle-related Disease Center, Japan Anti-Tuberculosis Association, Fukujuji Hospital, Tokyo, Japan.

Lena Eliasson (L)

Islet Cell Exocytosis, Lund University Diabetes Centre, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden. lena.eliasson@med.lu.se.
Clinical Research Centre, Skåne University Hospital, Lund and Malmö, Sweden. lena.eliasson@med.lu.se.

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Classifications MeSH