Abstract

Aureobasidium pullulans-derived β-glucan (AP-PG) consisting of a β-(1,3)-linked glucose main chain and β-(1,6)-linked glucose branches is taken as a supplement to improve health. This study demonstrates that oral administration of AP-PG is effective to prevent the development of high-fat diet (HFD)-induced fatty liver in mice. Here, C57BL/6N mice were fed with a normal diet or HFD, and AP-PG diluted in drinking water was administered orally. After 16 weeks, the serological analysis showed that HFD-induced high blood cholesterol and triglyceride levels were reduced by the oral administration of AP-PG. Further, HFD induced-fatty liver was significantly reduced by the oral administration of AP-PG. The triglyceride accumulation in the liver was also significantly reduced in mice administered AP-PG. Liver injury as indicated by an increase in serum alanine aminotransferase (ALT) in the HFD-fed mice was significantly reduced in the mice administered AP-PG orally, and the gene expression of cholesterol 7 alpha-hydroxylase (CYP7A1) which is known to be involved in cholesterol degradation in the liver was significantly increased in the AP-PG administered mice. These results suggest the possibility that the oral administration of AP-PG is effective to prevent the development of non-alcoholic fatty liver disease (NAFLD).

Highlights

  • Non-alcoholic fatty liver disease (NAFLD) is known to be a major health problem in many developed countries

  • In this study it is clearly demonstrated that orally administrated AP-PG is effective in reducing high-fat diet (HFD)-induced high serum cholesterol and triglyceride, HFD-induced adipose tissue hypertrophy, HFD-induced liver injury as indicated by the elevation of ALT, and HFD-induced fatty liver

  • We found that oral administration of AP-PG led to a significant up-regulation of HMGR and CYP7A1, rate-limiting enzymes for cholesterol synthesis and cholesterol degradation, respectively

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Summary

Introduction

Non-alcoholic fatty liver disease (NAFLD) is known to be a major health problem in many developed countries. Liver injury as indicated by an increase in serum alanine aminotransferase (ALT) in HFD-fed mice was significantly reduced by orally administered AP-PG, and the gene expression of cholesterol 7 alpha-hydroxylase (CYP7A1) which is known to be involved in cholesterol degradation in the liver was significantly increased in AP-PG administered mice. These results show the potential for β -glucan produced by A. pullulans as a supplemental food in the prevention of diseases caused by high fat diet life styles

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