The morphological changes and molecular biomarker responses in the liver of fluoride-exposed Bufo gargarizans larvae

Ecotoxicol Environ Saf. 2018 Apr 30;151:199-205. doi: 10.1016/j.ecoenv.2018.01.027. Epub 2018 Feb 4.

Abstract

The goal of the current study was to evaluate the negative influences of fluoride on liver of Bufo gargarizans larvae. B. gargarizans larvae were treated with 42.4mgF-/L for 0, 24, 48 and 72h at Gosner stage 37. The morphological changes and responses of molecular biomarkers involved in lipid metabolism, oxidative stress and apoptosis were examined in liver. Disappearance of cell boundaries, degeneration of hepatic parenchyma cells and significant increase in the number of melanomacrophage centres and the quantity of lipid droplets were found in the liver treated with 42.4mgF-/L for 72h. In addition, in the relative expression of acetyl CoA carboxylase 1 (ACC-1), fatty acid elongase 1 (FAE-1), sterol carrier protein 2 (SCP-2), and carnitine palmitoyltransferase-1 (CPT-1), decrease was observed after 24, 48 and 72h of 42.4mgF-/L exposure. Furthermore, the transcript levels of superoxide dismutase (SOD) and glutathione peroxidase (GPx) were downregulated in tadpoles exposed for 24, 48 and 72h to 42.4mgF-/L, while the transcript level of heat shock protein 90 (HSP90) was upregulated at 42.4mgF-/L for 72h. Also, mRNA expression of Bcl-2-associated transcription factor 1(BCLAF1) and thyroid hormone receptors (TRα and TRβ) was significantly upregulated in tadpoles treated with 42.4mgF-/L for 72h. Therefore, our results suggested that the liver injury induced by fluoride might result from disruption of lipid metabolism, oxidative damage and apoptosis.

Keywords: Apoptosis; Bufo gargarizans; Fluoride; Lipid metabolism; Oxidative stress.

MeSH terms

  • Acetyl-CoA Carboxylase / genetics
  • Acetyl-CoA Carboxylase / metabolism
  • Acetyltransferases / genetics
  • Acetyltransferases / metabolism
  • Animals
  • Biomarkers / metabolism*
  • Bufonidae / metabolism*
  • Carnitine O-Palmitoyltransferase / genetics
  • Carnitine O-Palmitoyltransferase / metabolism
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Chemical and Drug Induced Liver Injury / diagnosis
  • Chemical and Drug Induced Liver Injury / physiopathology
  • Fatty Acid Elongases
  • Female
  • Fluorides / toxicity*
  • Gene Expression Regulation
  • Glutathione Peroxidase / genetics
  • Glutathione Peroxidase / metabolism
  • Larva / drug effects*
  • Larva / metabolism
  • Lipid Metabolism / drug effects
  • Liver / drug effects*
  • Liver / metabolism
  • Male
  • Oxidative Stress / drug effects
  • RNA, Messenger
  • Receptors, Thyroid Hormone / genetics
  • Receptors, Thyroid Hormone / metabolism
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism

Substances

  • Biomarkers
  • Carrier Proteins
  • RNA, Messenger
  • Receptors, Thyroid Hormone
  • sterol carrier proteins
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Acetyltransferases
  • Fatty Acid Elongases
  • Carnitine O-Palmitoyltransferase
  • Acetyl-CoA Carboxylase
  • Fluorides