Influence of kiwifruit on gastric and duodenal inflammation-related gene expression in aspirin-induced gastric mucosal damage in rats

Sci Rep. 2020 Aug 3;10(1):13055. doi: 10.1038/s41598-020-70006-0.

Abstract

Kiwifruit (KF) contains bioactive compounds with potential anti-inflammatory properties. In this study, we investigated the protective effects of KF on gastric and duodenal damage induced by soluble aspirin in healthy rats. Sixty-four male Sprague Dawley rats were allocated to eight experimental treatments (n = 8) and the experimental diets were fed for 14 days ad libitum. The experimental diets were 20% fresh pureed KF (green-fleshed and gold-fleshed) or 10% glucose solution (control diet). A positive anti-inflammatory control treatment (ranitidine) was included. At the end of the 14-day feeding period, the rats were fasted overnight, and the following morning soluble aspirin (400 mg/kg aspirin) or water (control) was administered by oral gavage. Four hours after aspirin administration, the rats were euthanized and samples taken for analysis. We observed no significant ulcer formation or increase in infiltration of the gastric mucosal inflammatory cells in the rats with the aspirin treatment. Despite this, there were significant changes in gene expression, such as in the duodenum of aspirin-treated rats fed green KF where there was increased expression of inflammation-related genes NOS2 and TNF-alpha. We also observed that gold and green KF diets had a number of contrasting effects on genes related to inflammation and gastro-protective effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actinidia / chemistry*
  • Animals
  • Aspirin / adverse effects*
  • CLOCK Proteins / genetics
  • CLOCK Proteins / metabolism
  • Duodenum / drug effects
  • Duodenum / pathology*
  • Fruit / chemistry*
  • Gastric Mucosa / drug effects
  • Gastric Mucosa / metabolism
  • Gastric Mucosa / pathology*
  • Gene Expression Regulation* / drug effects
  • Inflammation / genetics*
  • Inflammation / pathology
  • Male
  • Plant Extracts / pharmacology
  • Plant Extracts / therapeutic use
  • Principal Component Analysis
  • Rats, Sprague-Dawley
  • Stomach / drug effects
  • Stomach / pathology*
  • Stomach Ulcer / drug therapy
  • Stomach Ulcer / genetics
  • Stomach Ulcer / pathology
  • Tight Junction Proteins / genetics
  • Tight Junction Proteins / metabolism
  • Tryptophan / metabolism

Substances

  • Plant Extracts
  • Tight Junction Proteins
  • Tryptophan
  • CLOCK Proteins
  • Aspirin