CD-1


Journal

Journal of diabetes investigation
ISSN: 2040-1124
Titre abrégé: J Diabetes Investig
Pays: Japan
ID NLM: 101520702

Informations de publication

Date de publication:
Nov 2020
Historique:
received: 24 12 2019
revised: 28 03 2020
accepted: 11 05 2020
pubmed: 31 5 2020
medline: 20 8 2021
entrez: 31 5 2020
Statut: ppublish

Résumé

To establish novel therapies to combat diabetic kidney disease, a human disease-relevant animal model is essential. However, a type 2 diabetic mouse model presenting progressive kidney fibrosis has not yet been established. Kidneys of streptozotocin-induced diabetic CD-1 mice showed severe fibrosis compared with other backgrounds of mice associated with the suppression of antifibrotic peptide N-acetyl-seryl-aspartyl-lysyl-proline. The BKS background (BKS We generated CD-1 Male CD-1 These results suggest that CD-1

Identifiants

pubmed: 32472621
doi: 10.1111/jdi.13311
pmc: PMC7610117
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1470-1481

Subventions

Organisme : Japan Society for the Promotion of Science
ID : 19K08738
Organisme : Japan Society for the Promotion of Science
ID : 26460403
Organisme : Japan Society for the Promotion of Science
ID : 25282028
Organisme : Japan Society for the Promotion of Science
ID : 25670414
Organisme : Grant for Promoted Research
ID : S2016-3
Organisme : Grant for Promoted Research
ID : S2017-1
Organisme : Kanazawa Medical University
ID : K2017-16

Informations de copyright

© 2020 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd.

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Auteurs

Yuiko Mizunuma (Y)

Department of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.
Department of Endocrinology and Metabolism, Dokkyo Medical University, Mibu, Tochigi, Japan.

Keizo Kanasaki (K)

Department of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.
Division of Anticipatory Molecular Food Science and Technology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.
Internal Medicine 1, Shimane University Faculty of Medicine, Izumo, Shimane, Japan.

Kyoko Nitta (K)

Department of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.

Yuka Nakamura (Y)

Medical Research Institute, Kanazawa Medical University, Uchinada, Ishikawa, Japan.

Yasuhito Ishigaki (Y)

Medical Research Institute, Kanazawa Medical University, Uchinada, Ishikawa, Japan.

Yuta Takagaki (Y)

Department of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.

Munehiro Kitada (M)

Department of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.
Division of Anticipatory Molecular Food Science and Technology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.

Shaolan Li (S)

Department of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.

Haijie Liu (H)

Department of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.

Jinpeng Li (J)

Department of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.

Isao Usui (I)

Department of Endocrinology and Metabolism, Dokkyo Medical University, Mibu, Tochigi, Japan.

Yoshimasa Aso (Y)

Department of Endocrinology and Metabolism, Dokkyo Medical University, Mibu, Tochigi, Japan.

Daisuke Koya (D)

Department of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.
Division of Anticipatory Molecular Food Science and Technology, Kanazawa Medical University, Uchinada, Ishikawa, Japan.

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Classifications MeSH