Literature DB >> 32979584

Interspecies differences in cytochrome P450-mediated metabolism of neonicotinoids among cats, dogs, rats, and humans.

Kraisiri Khidkhan1, Yoshinori Ikenaka2, Takahiro Ichise1, Shouta M M Nakayama1, Hazuki Mizukawa3, Kei Nomiyama4, Hisato Iwata4, Koji Arizono5, Keisuke Takahashi6, Keisuke Kato6, Mayumi Ishizuka7.   

Abstract

Neonicotinoid insecticides are used for agricultural and non-agricultural purposes worldwide. Pets are directly exposed to neonicotinoids in veterinary products and through environmental contamination. Cytochrome P450 (CYP) is among the most significant xenobiotic metabolizing enzymes that oxidizes several chemicals, including neonicotinoids. However, CYP activities and metabolite compositions of neonicotinoid metabolites are unknown in most domesticated pet species. Our objectives were to reveal the differences in metabolites of neonicotinoids (imidacloprid, clothianidin, and acetamiprid) and CYP activities among common pet species (cats and dogs), humans, and rats. The results indicated that the CYP-mediated neonicotinoid metabolism was different depending on species and each neonicotinoid. Among these four species, the kinetics of imidacloprid metabolism indicated that rats have the highest rate of oxidation of imidacloprid to 4OH-imidacloprid, while the greatest enzyme kinetics of imidacloprid metabolism to 5OH-imidacloprid were found in rats and humans. Clothianidin was rapidly metabolized to 1-methyl-3-nitroguanidine and dm-clothianidin in rats, but cats and humans showed the lowest formation of dm-clothianidin. CYP activities in metabolism of acetamiprid to dm-acetamiprid and N-acetyl-acetamiprid were determined to be significantly higher in humans compared to other species. However, further studies should be targeted at identifying the differences in hepatic metabolism of neonicotinoids in these species using recombinant CYP enzymes.
Copyright © 2020. Published by Elsevier Inc.

Entities:  

Keywords:  Cytochrome P450; In vitro microsomal assay; Neonicotinoids; Species variations

Mesh:

Substances:

Year:  2020        PMID: 32979584     DOI: 10.1016/j.cbpc.2020.108898

Source DB:  PubMed          Journal:  Comp Biochem Physiol C Toxicol Pharmacol        ISSN: 1532-0456            Impact factor:   3.228


  4 in total

1.  Human metabolism and urinary excretion of seven neonicotinoids and neonicotinoid-like compounds after controlled oral dosages.

Authors:  Sonja A Wrobel; Daniel Bury; Heiko Hayen; Holger M Koch; Thomas Brüning; Heiko U Käfferlein
Journal:  Arch Toxicol       Date:  2021-10-13       Impact factor: 5.153

2.  Use of transcriptomics in hazard identification and next generation risk assessment: A case study with clothianidin.

Authors:  Heike Sprenger; Katrin Kreuzer; Jimmy Alarcan; Kristin Herrmann; Julia Buchmüller; Philip Marx-Stoelting; Albert Braeuning
Journal:  Food Chem Toxicol       Date:  2022-06-08       Impact factor: 5.572

3.  Estimation of the Effects of Neonicotinoid Insecticides on Wild Raccoon, Procyon lotor, in Hokkaido, Japan: Urinary Concentrations and Hepatic Metabolic Capability of Neonicotinoids.

Authors:  So Shinya; Mariko Sashika; Miku Minamikawa; Tetsuji Itoh; Yared Beyene Yohannes; Shouta M M Nakayama; Mayumi Ishizuka; Collins Nimako; Yoshinori Ikenaka
Journal:  Environ Toxicol Chem       Date:  2022-06-09       Impact factor: 4.218

4.  Ca2+ imaging with two-photon microscopy to detect the disruption of brain function in mice administered neonicotinoid insecticides.

Authors:  Anri Hirai; Shouta Sugio; Collins Nimako; Shouta M M Nakayama; Keisuke Kato; Keisuke Takahashi; Koji Arizono; Tetsushi Hirano; Nobuhiko Hoshi; Kazutoshi Fujioka; Kumiko Taira; Mayumi Ishizuka; Hiroaki Wake; Yoshinori Ikenaka
Journal:  Sci Rep       Date:  2022-03-24       Impact factor: 4.379

  4 in total

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