d-Allose is absorbed via sodium-dependent glucose cotransporter 1 (SGLT1) in the rat small intestine.

Intestinal absorption SGLT1 d-Allose

Journal

Metabolism open
ISSN: 2589-9368
Titre abrégé: Metabol Open
Pays: England
ID NLM: 101767753

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 03 07 2021
revised: 19 07 2021
accepted: 21 07 2021
entrez: 12 8 2021
pubmed: 13 8 2021
medline: 13 8 2021
Statut: epublish

Résumé

d-Allose is the C3 epimer of d-glucose and has been reported to have beneficial health effects. The transporter mediating intestinal transport of d-allose is unknown. We examined whether d-allose is absorbed via sodium-dependent glucose cotransporter 1 (SGLT1) as well as via glucose transporter type 5 (GLUT5) using rats. For examination of absorption via SGLT1, KGA-2727, an SGLT1-specific inhibitor, and d-allose were orally administered. KGA-2727 blocked the increase of plasma d-allose levels and suppressed them throughout the experiment (0-180 min), whereas without KGA-2727, the plasma d-allose levels peaked at around 60-90 min. For examination of absorption via GLUT5, rats were fed a high-fructose diet for 3weeks to increase the abundance and activity of GLUT5 in the small intestine. High-fructose diet-fed rats did not exhibit significant changes in the plasma d-allose levels compared to control rats fed a high-glucose diet. These results indicate that SGLT1 but not GLUT5 mediates the intestinal absorption of d-allose.

Identifiants

pubmed: 34381987
doi: 10.1016/j.metop.2021.100112
pii: S2589-9368(21)00036-0
pmc: PMC8339219
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100112

Informations de copyright

© 2021 The Authors.

Déclaration de conflit d'intérêts

The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: T. Iida and T. Yamada are employed by Matsutani Chemical Industry Co., Ltd.

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Auteurs

Kunihiro Kishida (K)

Department of Science and Technology on Food Safety, Kindai University, 930 Nishimitani, Kinokawa, Wakayama, 649-6493, Japan.

Tetsuo Iida (T)

Research and Development, Matsutani Chemical Industry Company, Limited, 5-3 Kita-Itami, Itami, Hyogo, 664-8508, Japan.

Takako Yamada (T)

Research and Development, Matsutani Chemical Industry Company, Limited, 5-3 Kita-Itami, Itami, Hyogo, 664-8508, Japan.

Yukiyasu Toyoda (Y)

Department of Pathobiochemistry, Faculty of Pharmacy, Meijo University, 150 Yagotoyama, Tempaku-ku, Nagoya, Aichi, 468-8503, Japan.

Classifications MeSH