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.
Mice on a high-fat diet received oral A. pullulans beta-glucan for 16 weeks.
Lipid and liver-related measures improved in the animal model. Prevention or treatment of human fatty-liver disease was not tested.
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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.
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