Metabolomics reveals the reproductive abnormality in female zebrafish exposed to environmentally relevant levels of climbazole

Climbazole (CBZ) ubiquitously detected in the aquatic environment may disrupt fish reproductive function. Thus far, the previous study has focused on its transcriptional impact of steroidogenesis-related genes on zebrafish, but the underlying toxic mechanism still needs further investigation at the metabolic level. In this study, adult zebrafish were chronically exposed to CBZ at concentrations of 0.1 (corresponding to the real concentration in surface water), 10, and 1000 mu mg/L and evaluated for reproductive function by egg production, with subsequent ovarian tissue samples taken for histology, metabolomics, and other biochemical analysis. After 28 days' exposure, fecundity was significantly decreased in all exposure groups, with the inhibition of oocytes in varying developmental stages to a certain degree. The decrease in retinoic acid and sex hormones, down-regulated genes important in steroidogenesis, and increase in oxidized/reduced glutathione ratio and occurrence of apoptotic cells were observed in zebrafish ovaries following exposure to CBZ even at environmentally realistic concentrations, suggesting that alternations in steroidogenesis and oxidative stress can play significant roles in CBZ-triggered reproductive toxicity. Besides, mass spectrometry imaging analysis validated the results from metabolomics analysis. Our findings provide novel perspectives for unveiling the mechanism of reproductive dysfunction by CBZ and highlight its risk to fish reproduction. (C) 2021 Elsevier Ltd. All rights reserved.

Automated summary

This study found that exposure to climbazole in zebrafish significantly affects reproductive function, leading to decreased fecundity and inhibited cell development in the ovaries. Metabolomics analysis and other biochemical assays revealed that climbazole may trigger reproductive toxicity through alterations in steroidogenesis and oxidative stress, shedding new light on the mechanism of reproductive dysfunction caused by climbazole.