Captopril's influence on Danio rerio embryonic development: Unveiling significant toxic outcomes at environmentally relevant concentrations

• Published in: The Science of the total environment 2024-07, Vol.933, p.173179-173179, Article 173179
• Main Authors: García-Valdespino, Fernando, Elizalde-Velázquez, Gustavo Axel, Herrera-Vázquez, Selene Elizabeth, Gómez-Oliván, Leobardo Manuel
• Format: Article
• Language: English
• Subjects: Antihypertensive drug; Apoptosis; Embryonic damage; Oxidative damage; Zebrafish
• ISSN: 0048-9697; 1879-1026
• DOI: 10.1016/j.scitotenv.2024.173179

Anticipating a global increase in cardiovascular diseases, there is an expected surge in the use of angiotensin-converting enzyme inhibitors, notably captopril (CAP). This heightened usage raises significant environmental apprehensions, mainly due to limited knowledge regarding CAP's toxic effects on aquatic species. In response to these concerns, the current study aimed to tackle this knowledge gap by evaluating the potential influence of nominal concentrations of CAP (0.2–2000 μg/L) on the embryonic development of Danio rerio. The findings revealed that CAP at all concentrations, even at concentrations considered environmentally significant (0.2 and 2 μg/L), induced various malformations in the embryos, ultimately leading to their mortality. Main malformations included pericardial edema, craniofacial malformation, scoliosis, tail deformation, and yolk sac deformation. In addition, CAP significantly altered the antioxidant activity of superoxide dismutase and catalase across all concentrations. Simultaneously, it elevated lipid peroxidation levels, hydroperoxides, and carbonylic proteins in the embryos, eliciting a substantial oxidative stress response. Likewise, CAP, at all concentrations, exerted significant modulatory effects on the expression of genes associated with apoptosis (bax, bcl2, p53, and casp3), organogenesis (tbx2a, tbx2b, and irx3b), and ion exchange (slc12a1 and kcnj1) in Danio rerio embryos. Both augmentation and reduction in the expression levels of these genes characterized this modulation. The Pearson correlation analysis indicated a close association between oxidative damage biomarkers and the expression patterns of all examined genes with the elevated incidence of malformations and mortality in the embryos. In summary, it can be deduced that CAP poses a threat to aquatic species. Nevertheless, further research is imperative to enhance our understanding of the environmental implications of this pharmaceutical compound. [Display omitted] •Pericardial edema was the main malformation observed in exposed embryos.•Realistic concentrations of captopril prompted oxidative stress in organisms.•Apoptosis-, organogenesis-, and ion exchange- related genes were altered.•Edema formation might be a consequence of pronephros alterations in embryos.