Amelioration of ethanol induced apoptotic DNA damage and ulcerative injuries in the mice gastric tissues by starch oral administration

Toxicol Mech Methods. 2018 Feb;28(2):130-139. doi: 10.1080/15376516.2017.1373879. Epub 2017 Sep 11.

Abstract

Nowadays, gastric ulcers have become very common gastrointestinal disorders and numerous natural plant extracts exert promising anti-ulcerative effects. Therefore, this study was designed to evaluate the possible protective effect of dietary starch against ethanol induced gastric ulcers in mice. Post-administration of dietary starch for three consecutive days caused remarkable ameliorations in hemorrhagic lesions in gastric mucus and significant suppression in % incidence of ulceration, ulcer index and ulcer score induced by ethanol single administration. Indeed, deep ulceration, necrosis, disruption and degeneration in large areas of mucosa layer together with dense inflammatory cells infiltration and edema in sub-mucosal layer induced by ethanol administration were attenuated by starch post-administration and normalized the tissue architecture of the stomach. This potential protective effect could be attributed to the potent anti-oxidative capacity of starch that causes scavenger of the reactive oxygen species and thereby decreasing single and double DNA stranded break inductions and apoptotic DNA damage revealed by returning the p53 and caspase-3 expression levels to the normal level compared to the ethanol treated group. In conclusion, dietary starch has a potent therapeutic effect against ethanol induced gastric ulcer in mice via its free radical scavengers ability. Thus, we recommended further studies on its possible use as antiulcer drugs.

Keywords: DNA damage; Dietary starch; caspase-3; ethanol; gastric ulcer; oxidative stress and mice; p53.

MeSH terms

  • Administration, Oral
  • Animals
  • Anti-Ulcer Agents / administration & dosage
  • Anti-Ulcer Agents / therapeutic use*
  • Apoptosis / drug effects*
  • Caspase 3 / metabolism
  • Central Nervous System Depressants / toxicity*
  • Comet Assay
  • DNA Damage*
  • Ethanol / toxicity*
  • Gastrointestinal Hemorrhage / chemically induced
  • Gastrointestinal Hemorrhage / pathology
  • Gastrointestinal Hemorrhage / prevention & control
  • Mice
  • Oxidative Stress / drug effects
  • Starch / administration & dosage
  • Starch / therapeutic use*
  • Stomach Ulcer / chemically induced*
  • Stomach Ulcer / pathology
  • Stomach Ulcer / prevention & control*
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Anti-Ulcer Agents
  • Central Nervous System Depressants
  • Tumor Suppressor Protein p53
  • Ethanol
  • Starch
  • Casp3 protein, mouse
  • Caspase 3