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Canna starch improves immune functions and the intestinal environment in mice

The present study was conducted to elucidate the dietary effects of canna starch on the immune functions and intestinal luminal environment in mice. The amylose and resistant starch characteristics were determined for six types of starch, including edible canna. Canna starch was found to be higher i...

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Detalles Bibliográficos
Autores principales: TANAKA, Mamoru, KOIDA, Ayaka, MIYAZAKI, Akira, TABATA, Kazushi, TAKEI, Yuichiro, TANIMOTO, Yoshihumi, KAWAMURA, Mami, TSUZUKI, Masafumi, TAKAHASHI, Haruka, YANO, Tetsu, WATANABE, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMFH Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067328/
https://www.ncbi.nlm.nih.gov/pubmed/37016689
http://dx.doi.org/10.12938/bmfh.2022-068
Descripción
Sumario:The present study was conducted to elucidate the dietary effects of canna starch on the immune functions and intestinal luminal environment in mice. The amylose and resistant starch characteristics were determined for six types of starch, including edible canna. Canna starch was found to be higher in amylose and resistant starch compared with the other starches. BALB/c mice were fed 3.16% (low-canna group) and 6.32% (high-canna group) canna starch for 2 weeks, and then intestinal parameters were measured. Fecal IgA and mucin levels were markedly elevated by canna starch intake. IgA levels in serum and spleen lymphocytes were elevated by canna starch intake in the high-canna group, but not in the low-canna group. When the mice were fed canna starch, the cecum weight increased, and the pH in the cecum decreased. The high-canna group had significantly increased levels of Clostridium subcluster XIVa lactic acid, acetic acid, and n-butyric acid in the cecum compared with the control group. These results suggested that canna starch supplementation changed the intestinal microbiota and enhanced the intestinal immune and barrier functions and cecal organic acids in mice.