Effects of atrazine and curcumin exposure on TCMK-1 cells: Oxidative damage, pyroptosis and cell cycle arrest

Food Chem Toxicol. 2024 Mar:185:114483. doi: 10.1016/j.fct.2024.114483. Epub 2024 Jan 30.

Abstract

Atrazine (ATR), a commonly used herbicide, is highly bioaccumulative and toxic, posing a threat to a wide range of organisms. Curcumin has strong antioxidant properties. However, it is unclear whether curcumin counteracts cellular pyroptosis as well as cell cycle arrest induced by ATR exposure. Therefore, we conducted a study using TCMK-1 cells and established cell models by adding 139 μmol/L ATR and 20 μmol/L curcumin. The results showed that ATR exposure produced excessive reactive oxygen species (ROS), reduced activities of enzymes such as GSH-PX, SOD and Total Antioxidant Capacity, markedly increased the content of H2O2, disrupted the antioxidant system, activated Caspase-1, and the expression levels of the pyroptosis-related genes NLRP3, GSDMD, ASC, Caspase-1, IL-1β and IL-18 were increased. The simultaneous excess of ROS led to DNA damage, activation of P53 led to elevated expression levels of P53 and P21, as a consequence, the expression levels of cyclinE, CDK2 and CDK4 were reduced. These results suggest that Cur can modulate ATR exposure-induced pyroptosis as well as cell cycle arrest in TCMK-1 cells by governing oxidative stress.

Keywords: Atrazine; Cell cycle arrest; Curcumin; Oxidative stress; Pyroptosis.

MeSH terms

  • Antioxidants / pharmacology
  • Atrazine* / toxicity
  • Caspase 1 / genetics
  • Cell Cycle Checkpoints
  • Curcumin* / pharmacology
  • Hydrogen Peroxide / metabolism
  • Oxidative Stress
  • Pyroptosis
  • Reactive Oxygen Species / metabolism
  • Signal Transduction
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Reactive Oxygen Species
  • Atrazine
  • Curcumin
  • Antioxidants
  • Hydrogen Peroxide
  • Tumor Suppressor Protein p53
  • Caspase 1