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Di‐(2‐ethylhexyl) phthalate induces ferroptosis in prepubertal mouse testes via the lipid metabolism pathway.
- Source :
- Environmental Toxicology; Mar2024, Vol. 39 Issue 3, p1747-1758, 12p
- Publication Year :
- 2024
-
Abstract
- Di‐(2‐ethylhexyl) phthalate (DEHP), a widely used plasticizer, has been shown to cause reproductive toxicity, but the precise mechanism remains unclear. This study aimed to investigate the possible molecular mechanism of DEHP‐induced testicular damage. In vivo study, we administered different doses of DEHP (0, 250, and 500 mg/kg/day) to male C57BL/6 mice from 22 and 35 days after birth. We found that DEHP exposure induced histopathological alterations in prepubertal testes, and testicular lipidomics indicated notable alterations in lipid metabolism and significant enrichment of ferroptosis. Further tests showed that ferrous iron (Fe2+) and malondialdehyde (MDA) levels significantly increased after DEHP exposure. Western blotting revealed that DEHP exposure reduced glutathione peroxidase 4 (GPX4) expression, and elevated acyl coenzyme A synthetase long‐chain member 4 (ACSL4) and lysophosphatidylcholine acyltransferase 3 (LPCAT3) expression. The in vitro results were consistent with the in vivo results. When Leydig cells and Sertoli cells were treated with ferrostatin‐1 and monoethylhexyl phthalate (MEHP), MEHP‐induced increases in Fe2+ and MDA levels, accumulation of lipid reactive oxygen species, downregulation of GPX4, and upregulation of ACSL4 and LPCAT3 were reversed. Collectively, our findings suggested that aberrant lipid metabolism and ferroptosis may be involved in prepubertal DEHP exposure‐induced testicular damage. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 15204081
- Volume :
- 39
- Issue :
- 3
- Database :
- Complementary Index
- Journal :
- Environmental Toxicology
- Publication Type :
- Academic Journal
- Accession number :
- 175303514
- Full Text :
- https://doi.org/10.1002/tox.24065