Hylocereus polyrhizus Peel Extract Retards Alcoholic Liver Disease Progression by Modulating Oxidative Stress and Inflammatory Responses in C57BL/6 Mice

Nutrients. 2020 Dec 18;12(12):3884. doi: 10.3390/nu12123884.

Abstract

Alcoholic liver disease (ALD) has become a health problem as alcohol consumption has increased annually. Hepatic lipid accumulation, oxidative stress, and inflammation are important factors in the progression of ALD. Red pitaya (Hylocereus polyrhizus (Weber) Britt. & Rose) peel is rich in polyphenols and betanins, which possess antioxidative and anti-inflammatory properties. Therefore, the aim of this study was to investigate the effects of red pitaya peel extract (PPE) on ALD and explore the associated mechanisms. C57BL/6 J mice were administered an ethanol liquid diet for 11 weeks with or without two different doses of PPE (500 and 1000 mg/kg BW). PPE treatment significantly ameliorated liver injury and hepatic fat accumulation, and it improved hepatic lipid metabolism via increases in AMPK and PPAR-α protein expression and a decrease in SREBP-1 expression. In addition, PPE inhibited CYP2E1 and Nrf2 protein expression, reduced endotoxin levels in the serum, and decreased TLR4 and MyD88 expression and inflammatory cytokine TNF-α and IL-1β levels in the liver. In conclusion, these findings suggest that PPE may prevent the progression of ALD by modulating lipid metabolism and reducing oxidative stress and inflammatory responses.

Keywords: alcoholic liver disease; fatty liver; inflammation; oxidative stress; red pitaya.

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Animals
  • Cactaceae / chemistry*
  • Cytochrome P-450 CYP2E1 / metabolism
  • Disease Progression*
  • Ethanol
  • Fruit / chemistry*
  • Inflammation / prevention & control
  • Interleukin-1beta / metabolism
  • Lipid Metabolism / drug effects
  • Liver / metabolism
  • Liver Diseases, Alcoholic / etiology
  • Liver Diseases, Alcoholic / prevention & control*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Myeloid Differentiation Factor 88 / metabolism
  • NF-E2-Related Factor 2 / metabolism
  • Oxidative Stress / drug effects*
  • PPAR alpha / metabolism
  • Plant Extracts / pharmacology*
  • Sterol Regulatory Element Binding Protein 1 / metabolism
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Interleukin-1beta
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • NF-E2-Related Factor 2
  • Nfe2l2 protein, mouse
  • PPAR alpha
  • Plant Extracts
  • Srebf1 protein, mouse
  • Sterol Regulatory Element Binding Protein 1
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • Ethanol
  • Cytochrome P-450 CYP2E1
  • AMP-Activated Protein Kinases