Amino acids mixture ameliorates alcohol-induced liver and behavioral impairments by modulating Nrf2 and ethanol metabolism

  • Hyeongyeong Kim
  • , Hyung Joo Suh
  • , Kisoo Han
  • , Nari Kim
  • , Joon Young Shim
  • , Eun Young Jung*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

This study evaluated the protective effects of Amino Liver Mixture (ALM), a formulation of branched-chain amino acids, L-arginine, L-methionine, and L-alanine, against ethanol-induced hepatic and behavioral impairments. In vitro, ALM reduced reactive oxygen species and malondialdehyde, restored alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) activity, activated the Nrf2/Keap1/HO-1 pathway, and suppressed TNF-α, IL-6, and IL-1β expression. In vivo, ALM pretreatment in mice decreased serum ethanol, acetaldehyde, AST, ALT, and lactate dehydrogenase (LDH), while enhancing ADH and ALDH activity and downregulating CYP2E1. ALM also alleviated oxidative stress, restored antioxidant gene expression, and reduced hepatic inflammatory cytokines. Behavioral tests showed dose-dependent improvements in ethanol-induced motor coordination and anxiety-like behaviors. These findings demonstrate that ALM provides hepatoprotective and neurobehavioral benefits by modulating ethanol metabolism, oxidative stress, and inflammation, supporting its potential as a functional food for alcohol-related disorders.

Original languageEnglish
Article number107073
JournalJournal of Functional Foods
Volume134
DOIs
Publication statusPublished - 2025 Nov

Bibliographical note

Publisher Copyright:
Copyright © 2025. Published by Elsevier Ltd.

Keywords

  • Amino liver mixture
  • Ethanol metabolism
  • Motor coordination
  • Nrf2/Keap1/HO-1 pathway
  • Oxidative stress

ASJC Scopus subject areas

  • Medicine (miscellaneous)
  • Food Science
  • Nutrition and Dietetics

Fingerprint

Dive into the research topics of 'Amino acids mixture ameliorates alcohol-induced liver and behavioral impairments by modulating Nrf2 and ethanol metabolism'. Together they form a unique fingerprint.

Cite this