The long-term effects of norgestrel on the reproductive and thyroid systems in adult zebrafish at environmentally relevant concentrations.

Progestins are crucial steroid hormones that have attracted wide attention due to their endocrine disrupting effects in fish. The aim of this study is to investigate the effects of long-term exposure to low concentrations of norgestrel (NGT) on the reproductive and thyroid endocrine systems of adult zebrafish. Adult zebrafish were exposed to 7 and 39 ng/L NGT for a duration of 90 days. The results revealed that exposure to 39 ng/L NGT led to a significant up-regulation of 3ß-hydroxysteroid dehydrogenase (hsd3b) and 20ß-hydroxysteroid dehydrogenase (hsd20b) genes in the ovary of female zebrafish. Additionally, there was a significant up-regulation of 11ß-hydroxysteroid dehydrogenase 2 (hsd11b2) gene in the testis of male zebrafish. Furthermore, egg production decreased significantly, accompanied by notable alterations in the proportion of ovarian development stages, as well as reductions of sex hormone levels (E2, 11-KT, and T) in both females and males. However, long-term exposure to low concentrations of NGT did not lead to changes in thyroid hormone levels and thyroid histopathology in adult zebrafish. The overall results imply that environmental concentrations of NGT have a strong endocrine disrupting effect on the reproductive system of zebrafish, while the thyroid system is not sensitive to NGT exposure. The present study underscores the reproductive endocrine impacts of NGT and emphasizes the necessity for prolonged exposure at environmental concentrations.

Ferrate(vi) initiated oxidative degradation mechanisms clarified by DFT calculations: a case for sulfamethoxazole.

Ferrate(vi) is an efficient and environmentally friendly oxidant for the degradation of organic micropollutants. However, the related mechanism for the degradation is ambiguous and can hardly be elucidated empirically due to the rapid oxidation process and unstable intermediates for experimental trapping. Herein we performed density function theory (DFT) calculations to unveil the mechanism of ferrate(vi)-mediated degradation, taking sulfamethoxazole as a model compound. The results show that nucleophilic attack (rather than electrophilic attack) of HFeO4- on the isoxazole moiety of sulfamethoxazole initiates the subsequent degradations, and ferrate(vi) rather than the water molecule provides O atoms for the oxidation of the nitroso group and isoxazole moiety. Electron delocalization from the Fe atom to the isoxazole moiety is crucial for the ring-opening of isoxazole, and organometallic intermediates suggested previously are not the necessary ones in the oxidation of sulfamethoxazole by HFeO4-. Thus, this study has theoretically clarified the ferrate(vi) oxidation mechanisms for a representative sulfonamide, which were also partially corroborated by the intermediates and products observed in the previous experimental studies for phosphite and tryptophan. This study provides an exemplification on the application of quantum chemical calculations to clarify the degradation pathways of organic micropollutants, which is important for the prediction of degradation products needed in their engineering design.