Azoxystrobin at sub-cytotoxic concentrations disrupts intracellular zinc homeostasis: A flow cytometric analysis with rat thymic lymphocytes and fluorescent probes

Azoxystrobin is a broad-spectrum fungicide having a wide usage. However, the toxic effect of azoxystrobin in humans is not reported. In Japan, azoxystrobin was detected at a five-fold higher concentration than the normal upper limit (2.5 mg/kg) in a shipment of an Australian barley used in different...

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Veröffentlicht in:Fundamental Toxicological Sciences 2020, Vol.7(1), pp.1-7
Hauptverfasser: Shoji, Mai, Asada, Masaki, Matsumoto, Akihiko, Nishino, Haruki, Xiang, Ao Yi, Mizobuchi, Mizuki, Kanematsu, Naoki, Miura, Hajime, Kamemura, Norio
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Sprache:eng
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Zusammenfassung:Azoxystrobin is a broad-spectrum fungicide having a wide usage. However, the toxic effect of azoxystrobin in humans is not reported. In Japan, azoxystrobin was detected at a five-fold higher concentration than the normal upper limit (2.5 mg/kg) in a shipment of an Australian barley used in different food products. Thus, there is a chance of azoxystrobin exposure through food to humans, and hence it is imperative to study the toxic effects of this compound. In this study, the toxic effect of azoxystrobin was evaluated to predict its adverse effects on human. Azoxystrobin at 3-30 µM (approximately 1.2-12.1 mg/L) raised the intracellular Zn2+ concentration of rat thymic lymphocytes. This increase was due to an influx of extracellular Zn2+ and a release of intracellular Zn2+. Azoxystrobin partially inhibited the temperature-dependent Zn2+ influx, thus jeopardizing the cellular Zn2+ homeostasis. Because Zn2+ is an important intracellular messenger in lymphocytes, this altered Zn2+ homeostasis might lead to adverse effects if the blood concentration of azoxystrobin reaches 3 µM or more in humans. However, by extrapolating the azoxystrobin pharmacokinetics data of rats to human, it can be predicted that such high blood concentration may be unlikely in humans.
ISSN:2189-115X
2189-115X
DOI:10.2131/fts.7.1