Acute and chronic effects of the organophosphate malathion on the pancreatic α and β cell viability, cell structure, and voltage-gated K+ currents

Studies indicate that the pesticide malathion may have a role in diabetes. Herein, we determined the effects of different concentrations of malathion on survival, ultrastructure, and electrophysiologic islet cell parameters. Acutely, high concentrations of malathion (0.5 or 1 mM) increased cell deat...

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Published inEnvironmental toxicology and pharmacology Vol. 98; p. 104046
Main Authors Martins, J.R.N, Lopes, S., Hurtado, H.N., da Silva, F.N., Villard, D.R., Taboga, S.R., Souza, K.L.A, Quesada, I., Soriano, S., Rafacho, A.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.03.2023
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Summary:Studies indicate that the pesticide malathion may have a role in diabetes. Herein, we determined the effects of different concentrations of malathion on survival, ultrastructure, and electrophysiologic islet cell parameters. Acutely, high concentrations of malathion (0.5 or 1 mM) increased cell death in rat islet cells, while low concentrations (0.1 mM) caused signs of cell damage in pancreatic α and β cells. Exposure of RINm5F cells to malathion for 24 or 48 h confirmed the reduction in β-cell viability at lower concentrations (0.001–100 µM). Chronic exposure of mouse pancreatic α and β cells to 3 nM of malathion led to increased voltage-gated K+ (Kv) currents in α-cells. Our findings show a time and concentration dependency for the malathion effect on the reduction of islet cell viability and indicate that pancreatic α cells are more sensitive to malathion effects on Kv currents and cell death. [Display omitted] •Malathion causes degeneration of the basement membrane in rat pancreatic islets.•Malathion exposure leads to increased cell death in rat pancreatic islets.•Malathion increases autophagy and cell death in pancreatic rat α and β cells.•Immortalized RINm5F cells exposed to malathion have reduced cell viability.•Malathion causes increased K+ currents in mouse α cells but not in β cells.
ISSN:1382-6689
1872-7077
DOI:10.1016/j.etap.2022.104046