Identifying Candidate Flavonoids for Non-Alcoholic Fatty Liver Disease by Network-Based Strategy.

Front Pharmacol

Department of Physiology, College of Korean Medicine, Gachon University, Seongnam, South Korea.

Published: May 2022

AI Article Synopsis

  • NAFLD is the most common chronic liver disease with no guaranteed treatments, and this study aimed to find potential flavonoid candidates for its prevention and treatment.
  • A network-based approach combined data on flavonoid interactions with machine learning to identify and prioritize flavonoids based on their relationship to NAFLD-related proteins.
  • The study specifically highlighted glycitin as a promising candidate, demonstrating its ability to reduce lipid accumulation and oxidative stress-related reactions in liver cells, backed by molecular docking and gene expression validations.

Article Abstract

Nonalcoholic fatty liver disease (NAFLD) is the most common type of chronic liver disease and lacks guaranteed pharmacological therapeutic options. In this study, we applied a network-based framework for comprehensively identifying candidate flavonoids for the prevention and/or treatment of NAFLD. Flavonoid-target interaction information was obtained from combining experimentally validated data and results obtained using a recently developed machine-learning model, AI-DTI. Flavonoids were then prioritized by calculating the network proximity between flavonoid targets and NAFLD-associated proteins. The preventive effects of the candidate flavonoids were evaluated using FFA-induced hepatic steatosis in HepG2 and AML12 cells. We reconstructed the flavonoid-target network and found that the number of re-covered compound-target interactions was significantly higher than the chance level. Proximity scores have successfully rediscovered flavonoids and their potential mechanisms that are reported to have therapeutic effects on NAFLD. Finally, we revealed that discovered candidates, particularly glycitin, significantly attenuated lipid accumulation and moderately inhibited intracellular reactive oxygen species production. We further confirmed the affinity of glycitin with the predicted target using molecular docking and found that glycitin targets are closely related to several proteins involved in lipid metabolism, inflammatory responses, and oxidative stress. The predicted network-level effects were validated at the levels of mRNA. In summary, our study offers and validates network-based methods for the identification of candidate flavonoids for NAFLD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204489PMC
http://dx.doi.org/10.3389/fphar.2022.892559DOI Listing

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