» Articles » PMID: 24505260

3-Nitropropionic Acid Induces Ovarian Oxidative Stress and Impairs Follicle in Mouse

Overview
Journal PLoS One
Date 2014 Feb 8
PMID 24505260
Citations 39
Authors
Affiliations
Soon will be listed here.
Abstract

Oxidative stress induces many serious reproductive diseases in female mammals and thus poses a serious threat to reproductive health. However, the relationship between reactive oxygen species (ROS)-induced oxidative stress and follicular development, oocyte and embryo quality is not clear. The aim of this study was to investigate the effect of ovarian oxidative stress on the health of follicle and oocyte development. Female ICR mice were dosed with 3-nitropropionic acid (3-NPA) at three different concentrations (6.25, 12.5 and 25 mg/kg) and saline (control) via continuous intraperitoneal injection for 7 days. The treatment with 12.5 mg/kg reduced the weight of mouse ovaries, and significantly increased ROS levels and the activities of antioxidant enzymes--total superoxide dismutase (T-SOD), glutathione peroxidase (GPx) and catalase (CAT)--in granulosa cells and ovarian tissues, but not in other tissues (brain, liver, kidney and spleen). The same treatment significantly increased the percentage of atretic large follicles, and reduced the number of large follicles, the number of ovulated oocytes, and the capacity for early embryonic development compared with controls. It also significantly decreased the ratio of Bcl-2 to Bax, while causing an increase in the mRNA expression of (SOD2, CAT and GP X) and ROS levels in granulosa cells. Collectively, these data indicate that 3-NPA induces granulosa cell apoptosis, large follicle atresia, and an increase of ROS levels in the ovary. Therefore, we have established an in vivo model of ovarian oxidative stress for studying the mechanism of resulting damage induced by free radicals and for the screening of novel antioxidants.

Citing Articles

Quantitative Analysis of Flavonoids and Coumarins from Fingered Citron in Different Growth Periods and Their Regulatory Effects on Oxidative Stress.

Tan T, Xu M, Hong X, Li Z, Li J, Jiao B Foods. 2025; 14(2.

PMID: 39856847 PMC: 11765496. DOI: 10.3390/foods14020180.


Proanthocyanidins protects 3-NPA-induced ovarian function decline by activating SESTRIN2-NRF2-mediated oxidative stress in mice.

Huang Y, Cui Y, Huang J, Xinyuan H, Zihang W, Luo T Sci Rep. 2024; 14(1):25643.

PMID: 39465303 PMC: 11514188. DOI: 10.1038/s41598-024-76743-w.


Which is the current knowledge on man-made endocrine- disrupting chemicals in follicular fluid? An overview of effects on ovarian function and reproductive health.

Shulhai A, Bianco V, Donini V, Esposito S, Street M Front Endocrinol (Lausanne). 2024; 15:1435121.

PMID: 39415794 PMC: 11479995. DOI: 10.3389/fendo.2024.1435121.


Paeoniflorin Promotes Ovarian Development in Mice by Activating Mitophagy and Preventing Oxidative Stress.

Xi H, Wang Z, Li M, Duan X, Li Y Int J Mol Sci. 2024; 25(15).

PMID: 39125927 PMC: 11313479. DOI: 10.3390/ijms25158355.


Variations of plasma oxidative stress levels in male patients with chronic schizophrenia. Correlations with psychopathology and matrix metalloproteinase-9: a case-control study.

Yang H, Zhang C, Yang M, Liu J, Zhang Y, Liu D BMC Psychiatry. 2024; 24(1):20.

PMID: 38172869 PMC: 10765744. DOI: 10.1186/s12888-023-05479-0.


References
1.
Hoyer P, Devine P, Hu X, Thompson K, Sipes I . Ovarian toxicity of 4-vinylcyclohexene diepoxide: a mechanistic model. Toxicol Pathol. 2001; 29(1):91-9. DOI: 10.1080/019262301301418892. View

2.
Cawthon R . Telomere measurement by quantitative PCR. Nucleic Acids Res. 2002; 30(10):e47. PMC: 115301. DOI: 10.1093/nar/30.10.e47. View

3.
Farzaneh-Far R, Lin J, Epel E, Lapham K, Blackburn E, Whooley M . Telomere length trajectory and its determinants in persons with coronary artery disease: longitudinal findings from the heart and soul study. PLoS One. 2010; 5(1):e8612. PMC: 2797633. DOI: 10.1371/journal.pone.0008612. View

4.
Taupeau C, Poupon J, Nome F, Lefevre B . Lead accumulation in the mouse ovary after treatment-induced follicular atresia. Reprod Toxicol. 2001; 15(4):385-91. DOI: 10.1016/s0890-6238(01)00139-3. View

5.
Borgeest C, Symonds D, Mayer L, Hoyer P, Flaws J . Methoxychlor may cause ovarian follicular atresia and proliferation of the ovarian epithelium in the mouse. Toxicol Sci. 2002; 68(2):473-8. DOI: 10.1093/toxsci/68.2.473. View