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In Vivo 2015

Oral administration of the Aureobasidium pullulans-derived β-glucan effectively prevents the development of high fat diet-induced fatty liver in mice

Aoki, Shiho; Iwai, Atsushi; Kawata, Koji; Muramatsu, Daisuke; Uchiyama, Hirofumi; Okabe, Mitsuyasu; Ikesue, Masahiro; Maeda, Naoyoshi; Uede, Toshimitsu · Scientific Reports · DOI: 10.1038/srep10457
Research Archive
TL;DR — Key Findings
  • A. pullulans beta-glucan was studied in high-fat-diet-fed mice.
  • Treated mice showed changes in blood lipids, liver fat, ALT, and CYP7A1 expression.
  • The animal results do not establish prevention or treatment of fatty liver in humans.

Abstract

This animal study tested orally administered Aureobasidium pullulans-derived beta-glucan in mice fed a high-fat diet for 16 weeks. Compared with high-fat-diet controls, treated mice showed lower blood cholesterol and triglyceride measurements, less liver fat accumulation, lower serum alanine aminotransferase, and higher liver expression of CYP7A1, a gene involved in cholesterol metabolism. These results suggest a possible metabolic effect in this experimental model. They do not establish that the preparation prevents or treats fatty-liver disease in humans, and differences in dose, metabolism, and disease biology limit direct translation.

Summary

Summary

Study design

Mice on a high-fat diet received oral A. pullulans beta-glucan for 16 weeks.

Interpretation

Lipid and liver-related measures improved in the animal model. Prevention or treatment of human fatty-liver disease was not tested.

AI-generated summary for accessibility. Always refer to the original paper.

Citation

Aoki, Shiho; Iwai, Atsushi; Kawata, Koji; Muramatsu, Daisuke; Uchiyama, Hirofumi; Okabe, Mitsuyasu; Ikesue, Masahiro; Maeda, Naoyoshi; Uede, Toshimitsu. Oral administration of the Aureobasidium pullulans-derived β-glucan effectively prevents the development of high fat diet-induced fatty liver in mice. Scientific Reports. 2015. DOI: 10.1038/srep10457.

Study Details
Study Type
In Vivo
Published
2015
Journal
Scientific Reports
Authors
Aoki, Shiho; Iwai, Atsushi; Kawata, Koji; Muramatsu, Daisuke; Uchiyama, Hirofumi; Okabe, Mitsuyasu; Ikesue, Masahiro; Maeda, Naoyoshi; Uede, Toshimitsu
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