Platycodi Radix extract prevents hepatic steatosis by enhancing bile acid synthesis in a high-fat diet-induced fatty liver mouse model

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Title
Platycodi Radix extract prevents hepatic steatosis by enhancing bile acid synthesis in a high-fat diet-induced fatty liver mouse model
Author(s)
Wooyoung Kim; W H Baek; S H Yun; Hayoung Lee; Mi Jeong Kim; S Y Lee; G H Kim; S I Kim; H G Jeong; Edmond Changkyun Park
Bibliographic Citation
Nutrients, vol. 16, no. 6, pp. 893-893
Publication Year
2024
Abstract
We aimed to identify the mechanism underlying the preventive effects of non-alcoholic fatty liver disease (NAFLD) through Platycodi Radix consumption using liver proteomic and bioinformatic analysis. C57BL/6J mice were categorized into three groups: those receiving a standard chow diet (NCD), those on a high-fat diet (HFD), and those on an HFD supplemented with 5% Platycodi Radix extract (PRE). After a 12-week period, PRE-fed mice exhibited a noteworthy prevention of hepatic steatosis. Protein identification and quantification in liver samples were conducted using LC-MS/MS. The identified proteins were analyzed through Ingenuity Pathway Analysis software, revealing a decrease in proteins associated with FXR/RXR activation and a concurrent increase in cholesterol biosynthesis proteins in the PRE-treated mouse liver. Subsequent network analysis predicted enhanced bile acid synthesis from these proteins. Indeed, the quantity of bile acids, which was reduced in HFD conditions, increased in the PRE group, accompanied by an elevation in the expression of synthesis-related proteins. Our findings suggest that the beneficial effects of PRE in preventing hepatic steatosis may be mediated, at least in part, through the modulation of FXR/RXR activation, cholesterol biosynthesis, and bile acid synthesis pathways.
Keyword
ProteomicsCholesterolBile acidNon-alcoholic fatty liver disease (NAFLD)ObesityPlatycodon grandiflorumPlatycodi Radix
ISSN
2072-6643
Publisher
MDPI
Full Text Link
http://dx.doi.org/10.3390/nu16060893
Type
Article
Appears in Collections:
Division of A.I. & Biomedical Research > Immunotherapy Research Center > 1. Journal Articles
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