TY - JOUR
T1 - Exposure to Zinc Oxide Nanoparticles Increases Estradiol Levels and Induces an Antioxidant Response in Antral Ovarian Follicles In Vitro
AU - Santacruz-Márquez, Ramsés
AU - Flaws, Jodi A.
AU - Sánchez-Peña, Luz del Carmen
AU - Hernández-Ochoa, Isabel
N1 - Funding Information:
The authors want to thank the excellent assistance of Ángel Barrera Hernández, supervision of Luz María Del Razo, and the LISTO (Department of Toxicology, Cinvestav, Mexico) for the ICP-MS analyses. They thank Sihomara García Zepeda from the Department of Toxicology, Cinvestav, for her technical assistance. They also thank Andrea De Vizcaya for providing the gifted ZnO nanoparticles. They also thank all members of Flaws’ laboratory, in particular, Liying Gao for her technical assistance. RSM was enrolled in a PhD Toxicology program at Cinvestav and was recipient of a scholarship for graduate students (No. 429019) from the National Council of Science and Technology-Mexico (CONACyT-Mexico).
Publisher Copyright:
© 2023 by the authors.
PY - 2023/7
Y1 - 2023/7
N2 - The use of zinc oxide nanoparticles (ZnO NP) in consumer products is increasing, raising concern about their potential toxicity to human health. Nanoparticles have endocrine disrupting effects and can induce oxidative stress, leading to biomolecule oxidation and cell dysfunction. The ovary is one of the most important endocrine organs in female reproduction. Nanoparticles accumulate in the ovary, but it is unknown whether and how exposure to these materials disrupts antral follicle functions. Thus, this study tested the hypothesis that the in vitro exposure to ZnO NPs affects the steroidogenic pathway and induces oxidative stress in ovarian antral follicles. Antral follicles from CD-1 mice were cultured with ZnO NPs (5, 10, and 15 µg/mL) for 96 h. ZnO NP exposure did not affect apoptosis and cell cycle regulators at any of the tested concentrations. ZnO NP exposure at low levels (5 µg/mL) increased aromatase levels, leading to increased estradiol levels and decreased estrogen receptor alpha (Esr1) expression. ZnO NP exposure at 15 µg/mL induced an antioxidant response in the antral follicles as evidenced by changes in expression of antioxidant molecules (Nrf2, Cat, Sod1, Gsr, Gpx) and decreased levels of reactive oxygen species. Interestingly, ZnO NPs dissolve up to 50% in media and are internalized in cells as soon as 1 h after culture. In conclusion, ZnO NPs are internalized in antral follicles, leading to increased estrogen production and an antioxidant response.
AB - The use of zinc oxide nanoparticles (ZnO NP) in consumer products is increasing, raising concern about their potential toxicity to human health. Nanoparticles have endocrine disrupting effects and can induce oxidative stress, leading to biomolecule oxidation and cell dysfunction. The ovary is one of the most important endocrine organs in female reproduction. Nanoparticles accumulate in the ovary, but it is unknown whether and how exposure to these materials disrupts antral follicle functions. Thus, this study tested the hypothesis that the in vitro exposure to ZnO NPs affects the steroidogenic pathway and induces oxidative stress in ovarian antral follicles. Antral follicles from CD-1 mice were cultured with ZnO NPs (5, 10, and 15 µg/mL) for 96 h. ZnO NP exposure did not affect apoptosis and cell cycle regulators at any of the tested concentrations. ZnO NP exposure at low levels (5 µg/mL) increased aromatase levels, leading to increased estradiol levels and decreased estrogen receptor alpha (Esr1) expression. ZnO NP exposure at 15 µg/mL induced an antioxidant response in the antral follicles as evidenced by changes in expression of antioxidant molecules (Nrf2, Cat, Sod1, Gsr, Gpx) and decreased levels of reactive oxygen species. Interestingly, ZnO NPs dissolve up to 50% in media and are internalized in cells as soon as 1 h after culture. In conclusion, ZnO NPs are internalized in antral follicles, leading to increased estrogen production and an antioxidant response.
KW - nanoparticles
KW - endocrine disruptors
KW - hormones
KW - toxicity
KW - ovary
KW - antral follicles
KW - ZnO nanoparticles
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U2 - 10.3390/toxics11070602
DO - 10.3390/toxics11070602
M3 - Article
C2 - 37505567
SN - 2305-6304
VL - 11
JO - Toxics
JF - Toxics
IS - 7
M1 - 602
ER -