Mechanism of the Effect of Compound Anoectochilus roxburghii (Wall.) Lindl. Oral Liquid in Treating Alcoholic Rat Liver Injury by Metabolomics

Drug Des Devel Ther. 2023 Nov 15:17:3409-3428. doi: 10.2147/DDDT.S427837. eCollection 2023.

Abstract

Purpose: Compound Anoectochilus roxburghii (Wall.) Lindl oral liquid (CAROL) is often as a hepatoprotective agent. The present study aimed to elucidate the protective mechanism of CAROL against alcoholic liver injury in rats by untargeted metabolomics combined with multivariate statistical analysis.

Methods: An alcoholic liver disease model was established in sprague-dawley (SD) rats by gavage of alcohol, and CAROL treatment was administered. The hepatoprotective effect of CAROL was evaluated by examining liver tissues changes and detecting biochemical index activities and cytokines in serum and liver homogenates. The metabolites in serum samples were examined using ultrahigh-performance liquid chromatography quadrupole time-of-flight mass spectrometry (UHPLC-QTOF/MS) and multivariate statistical analysis to screen for differentially expressed metabolites and Kyoto Encyclopedia of Genes and Genomes (KEGG) to assess potential metabolic pathways.

Results: CAROL has the potential to downregulate inflammation levels and alleviate oxidative stress. The differential metabolites are mainly engaged in riboflavin metabolism, arginine and proline metabolism, phenylalanine, tyrosine and tryptophan biosynthesis metabolism, phenylalanine metabolism, pyrimidine metabolism, and vitamin B6 metabolism to achieve hepatoprotective effects.

Conclusion: CAROL may exhibit beneficial hepatoprotective effects by reducing inflammation, mitigating oxidative stress, and modulating metabolites and their metabolic pathways.This study has important implications for advancing the clinical application of CAROL.

Keywords: UHPLC–QTOF/MS; alcoholic liver injury; compound Anoectochilus roxburghii (Wall.) Lindl. oral liquid; metabolic pathway analysis; untargeted metabolomics.

MeSH terms

  • Animals
  • Chromatography, High Pressure Liquid / methods
  • Inflammation
  • Liver*
  • Metabolomics* / methods
  • Phenylalanine
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Phenylalanine

Grants and funding

This work was supported by the Natural Fund Project of Fujian Province, China (No. 2020J01623 and 2023J01311), the Joint Funds at the Innovation of Science and Technology, Fujian Province, China (No. 2021Y9008), the Young Teachers Education Foundation of Fujian Province, China (No. JAT220080), the High-Level Talent Foundation of Fujian Medical University (No. XRCZX2021005).