1. Effects of BPA, BPS, and BPF on Oxidative Stress and Antioxidant Enzyme Expression in Bovine Oocytes and Spermatozoa
- Author
-
Mimi Nguyen, Reem Sabry, Ola S. Davis, and Laura A. Favetta
- Subjects
Male ,bisphenol F ,endocrine system ,urogenital system ,bisphenol A ,Free Radical Scavengers ,QH426-470 ,bisphenol S ,oocytes ,spermatozoa ,oxidative stress ,Antioxidants ,Article ,Phenols ,Genetics ,Animals ,Cattle ,Female ,Sulfones ,Benzhydryl Compounds ,Genetics (clinical) ,reproductive and urinary physiology ,hormones, hormone substitutes, and hormone antagonists - Abstract
Bisphenol A (BPA) and its analogs, bisphenol S (BPS) and bisphenol F (BPF), might impact fertility by altering oxidative stress pathways. Here, we hypothesize that bisphenols-induced oxidative stress is responsible for decreased gamete quality. In both female (cumulus-oocyte-complexes—COCs) and male (spermatozoa), oxidative stress was measured by CM-H2DCFDA assay and key ROS scavengers (SOD1, SOD2, GPX1, GPX4, CAT) were quantified at the mRNA and protein levels using qPCR and Western blot (COCs)/immunofluorescence (sperm). Either gamete was treated in five groups: control, vehicle, and 0.05 mg/mL of BPA, BPS, or BPF. Our results show elevated ROS in BPA-treated COCs but decreased production in BPS- and BPF-treated spermatozoa. Additionally, both mRNA and protein expression of SOD2, GPX1, and GPX4 were decreased in BPA-treated COCs (p < 0.05). In sperm, motility (p < 0.03), but not morphology, was significantly altered by bisphenols. SOD1 mRNA expression was significantly increased, while GPX4 was significantly reduced. These results support BPA’s ability to alter oxidative stress in oocytes and, to a lesser extent, in sperm. However, BPS and BPF likely act through different mechanisms.
- Published
- 2022