Colonic metabolites from digested Moringa oleifera leaves induced HT-29 cell death via apoptosis, necrosis, and autophagy

Int J Food Sci Nutr. 2021 Jun;72(4):485-498. doi: 10.1080/09637486.2020.1849039. Epub 2020 Dec 10.

Abstract

Colorectal cancer is an important concern in modern society. Risk factors such as the diet indicate the need to find healthy food products displaying additional health benefits. This study aimed to characterise and evaluate the impact of the colonic metabolites from the fermented non-digestible fraction of Moringa oleifera (MO) leaves (FNFM) on cell death mechanisms from HT-29 cells. MO leaves were digested in vitro, and the 12 h-colonic extract was obtained. FNFM mainly contained morin and chlorogenic acids (41.97 and 25.33 µg/g sample). Butyric acid was ranked as the most important metabolite of FNFM. The FNFM exerted antiproliferative effect against HT-29 colorectal cancer cells (half lethal concentration, LC50: 5.9 mL/100 mL). Compared to untreated control, LC50 increased H2O2 production (149.43%); induced apoptosis (119.02%), autophagy (75.60%), and necrosis (87.72%). These results suggested that digested MO colonic metabolites exert antiproliferative effect against HT-29 cells, providing additional health benefits associated with MO consumption.

Keywords: Moringa oleifera; apoptosis; autophagy; colonic metabolites; colorectal cancer; short-chain fatty acids.

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Autophagy / drug effects*
  • Colon / metabolism*
  • Colorectal Neoplasms / drug therapy
  • Colorectal Neoplasms / metabolism
  • Fatty Acids, Volatile / metabolism
  • Fermentation
  • HT29 Cells
  • Humans
  • Hydrogen Peroxide / metabolism
  • Male
  • Moringa oleifera / chemistry*
  • Necrosis / drug therapy*
  • Plant Extracts / pharmacology*
  • Plant Leaves / chemistry*
  • Rats
  • Rats, Wistar

Substances

  • Fatty Acids, Volatile
  • Plant Extracts
  • Hydrogen Peroxide