The stereoselective metabolic disruption of cypermethrin by a sub-acute study based on metabolomics

Author:

Gu Sijia1,Zhang Quan1ORCID,Gu Jinping1,Wang Cui2,Chu Mengjie1,Li Jing1,Mo Xunjie1

Affiliation:

1. Zhejiang University of Technology

2. Zhejiang Chinese Medical University

Abstract

Abstract Due to the massive application of cypermethrins (CYPs) for pest control in China, the adverse effects on non-target organisms have aroused great attention. However, comparative studies between its different stereoisomers remain scarce, especially for metabolism perturbations. Herein, the rats were administered α-CYP, β-CYP and θ-CYP by gavage at doses of 8.5, 29.2 and 25.0 mg/kg, respectively, for 28 consecutive days. By blood examination, significant changes in liver and renal function parameters were observed in rats exposed to all three CYPs. The stereoisomeric selectivity in metabolism was assessed based on a metabolomic strategy via principal component analysis (PCA), orthogonal partial least squares discriminant analysis (OPLS-DA) and pathway analysis. The results demonstrated that amino acid and glycolipid metabolism were disrupted in all CYP groups. Among them, the most significant changes in the metabolic phenotype were observed in the θ-CYP group, with 56 differential metabolites enriched in 9 differential metabolic pathways. Perturbations in the alpha-linolenic acid metabolism associated with inflammation occurred only in the θ-CYP group of rats. At the same time, the endogenous metabolite trimethylamine oxide (TMAO), which is closely linked to the gut microbiota, was also significantly elevated in this group. Gender differences were evident in α- and θ-CYP-exposed rats, with perturbations in amino acid and glucose metabolism of greater concern in females and lipid metabolism of greater concern in males. Overall, β-CYP exhibited a lower risk of metabolic perturbations than α-CYP or θ-CYP, which helps to screen suitable agrochemical products for green agricultural development.

Publisher

Research Square Platform LLC

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