ATR induces hepatic lipid metabolism disorder in rats by activating IRE1α/XBP1 signaling pathway

Toxicology. 2024 Jan:501:153696. doi: 10.1016/j.tox.2023.153696. Epub 2023 Dec 6.

Abstract

Atrazine (ATR) is a widely used herbicide and due to its persistence in environment and bioaccumulation, it can cause harmful impacts on human health. ATR exposure can lead to disorders of lipid metabolism in the liver, but its underlying mechanism is still unclear. 40 eight-week-old rats were given different doses of ATR (0, 0.5, 5 and 50 mg/kg/d) for 90 days. The liver tissue and serum were collected for histological observation and biochemical analysis. The levels of lipid and oxidative stress were assessed using colorimetry. Changes in MMP and ROS of liver cells were observed through flow cytometry. The expression of mRNA and protein was detected using Real-Time PCR and western blot. The results showed that TC and HDL-C levels in both the liver and serum were increased in the ATR-treated groups. The levels of MDA were accumulated, while the levels of SOD and GSH were depleted in the liver with ATR exposure. The expression of liver lipid metabolism related genes (SCD1, DGAT2, ACC1, PPARγ) was elevated. The liver ERS was activated and the gene expression of IRE1α/XBP1 signal pathway and GRP78, GRP94 in the liver was increased. There was a correlation between the levels of ERS and the levels of lipid metabolism. These results suggested that ATR can activate ERS and promote the expression of IRE1α/XBP1 signaling pathway, and further lead to lipid metabolism disorders in rat liver. This study can provide valuable insights as a reference for the prevention and control of hazards associated with agricultural residues.

Keywords: Atrazine; ERS; IRE1α/XBP1; Liver lipid metabolism; Pesticide.

MeSH terms

  • Animals
  • Ataxia Telangiectasia Mutated Proteins / metabolism
  • Atrazine*
  • Endoribonucleases / metabolism
  • Humans
  • Lipid Metabolism
  • Lipid Metabolism Disorders* / metabolism
  • Liver / metabolism
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Rats
  • Signal Transduction
  • X-Box Binding Protein 1

Substances

  • Atrazine
  • Endoribonucleases
  • Protein Serine-Threonine Kinases
  • ATR protein, human
  • Ataxia Telangiectasia Mutated Proteins
  • XBP1 protein, human
  • X-Box Binding Protein 1