Hematological and Hepatic Effects of Ulexite in Zebrafish

Environ Toxicol Pharmacol. 2020 Nov:80:103496. doi: 10.1016/j.etap.2020.103496. Epub 2020 Sep 16.

Abstract

The ulexite (UX), a borate mineral, is used as boron source and commonly used in various industrial processes. The hematological and hepatic effects of UX were investigated by exposing adult zebrafish to UX (5, 10, 20 and 40 mg/L) over 96 hours. The blood and liver tissues were taken at the end of the trial period then micronucleus (MN) rates, oxidative DNA damage (8-OHdG), apoptosis (Caspase-3), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), myeloperoxidase (MPO), paraoxonase (PON), arylesterase (AR) and lipid peroxidation (MDA) levels were determined. Genotoxic damage by UX occurred only at 40 mg/L in the blood MN assay. Oxidative stress, oxidative DNA damage and apoptosis in liver also occurred at this dose. Moreover, 5-20 mg/L doses led to decreases of DNA damage and apoptosis levels via promoting antioxidant system in liver tissues. UX exhibits beneficial roles on blood and liver tissues of zebrafish at relatively lower doses, which may be relevant to nutritional and medicinal industries.

Keywords: DNA damage; Ulexite; apoptosis; blood; boron; liver; micronucleus frequency; nuclear abnormality; zebrafish.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Aryldialkylphosphatase / metabolism
  • Borates / pharmacology*
  • Carboxylic Ester Hydrolases / metabolism
  • Catalase / metabolism
  • DNA Damage
  • Erythrocytes / drug effects*
  • Erythrocytes / metabolism
  • Glutathione Peroxidase / metabolism
  • Lipid Peroxidation / drug effects
  • Liver / drug effects*
  • Liver / metabolism
  • Micronucleus Tests
  • Minerals / pharmacology*
  • Oxidative Stress / drug effects
  • Superoxide Dismutase / metabolism
  • Zebrafish* / genetics
  • Zebrafish* / metabolism

Substances

  • Borates
  • Minerals
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Carboxylic Ester Hydrolases
  • arylesterase
  • Aryldialkylphosphatase