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 in | Environmental toxicology and pharmacology Vol. 98; p. 104046 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.03.2023
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Subjects | |
Online Access | Get full text |
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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.
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•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. |
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ISSN: | 1382-6689 1872-7077 |
DOI: | 10.1016/j.etap.2022.104046 |