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Absorption, distribution, metabolism, and elimination of epoxiconazole enantiomers in lizards (Eremias argus).
- Source :
-
Chemosphere . Jul2024, Vol. 360, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- Epoxiconazole (EPX) is a world widely used chiral triazole fungicide in the agriculture field. The excessive application of this triazole may cause damage to lizards. However, limited information is known about the toxicokinetics of EPX on lizards. Our study aimed to investigate the enantioselective absorption, distribution, metabolism, and elimination (ADME) of EPX in lizards following low and high dose exposure (10 and 100 mg kg−1 bodyweitht (bw)). The results demonstrated that (+)-EPX was easier absorbed than (−)-EPX in lizard plasma. Both (+)-EPX and (−)-EPX were detected in the liver, gonad, kidney, skin, brain, and intestine, with (+)-EPX preferentially distributed in these tissues. The elimination of (−)-EPX was faster than that of (+)-EPX in lizard liver and kidney in the high dose groups. Chiral conversion was found between EPX enantiomers in lizard skin. Simultaneously, five metabolites including M2, M4, M10, M18 and M19 were detected in lizard liver and kidney after EPX enantiomers exposure. The relative concentrations of M2, M4, and M10 were higher in the liver and kidney of (−)-EPX groups than those produced from (+)-EPX groups. The metabolic enzymes CYP3A4 and SULT1A1 primarily mediated enantioselective metabolism of EPX. The conclusions drawn from this study significantly enhance our understanding of the enantioselective behaviors of chiral triazole fungicides in reptiles, offering essential guidance for assessing the risks associated with different enantiomers of triazole fungicides. [Display omitted] • (+)-EPX was easier absorbed than (−)-EPX in lizard plasma. • (+)-EPX was preferentially distributed in the liver, intestine, skin, gonad, brain, and kidney. • (−)-EPX was eliminated faster than (+)-EPX in the liver and kidney. • Chiral conversion was found between EPX enantiomers in the skin. • Relative concentrations of M2, M4, M10 in (−)-EPX groups were higher than in (+)-EPX groups. [ABSTRACT FROM AUTHOR]
- Subjects :
- *LIZARDS
*GONADS
*METABOLISM
*EXPOSURE dose
*ABSORPTION
*TRIAZOLES
*ENANTIOMERS
Subjects
Details
- Language :
- English
- ISSN :
- 00456535
- Volume :
- 360
- Database :
- Academic Search Index
- Journal :
- Chemosphere
- Publication Type :
- Academic Journal
- Accession number :
- 177750245
- Full Text :
- https://doi.org/10.1016/j.chemosphere.2024.142444