3-Nitropropionic acid induces ovarian oxidative stress and impairs follicle in mouse

PLoS One. 2014 Feb 5;9(2):e86589. doi: 10.1371/journal.pone.0086589. eCollection 2014.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antihypertensive Agents / pharmacology*
  • Apoptosis / drug effects*
  • Female
  • Follicular Atresia / drug effects*
  • Granulosa Cells / metabolism*
  • Granulosa Cells / pathology
  • Mice
  • Mice, Inbred ICR
  • Nitro Compounds / pharmacology*
  • Oxidative Stress / drug effects*
  • Oxidoreductases / metabolism
  • Propionates / pharmacology*
  • Reactive Oxygen Species / metabolism
  • bcl-2-Associated X Protein / metabolism

Substances

  • Antihypertensive Agents
  • Bax protein, mouse
  • Nitro Compounds
  • Propionates
  • Reactive Oxygen Species
  • bcl-2-Associated X Protein
  • Oxidoreductases
  • 3-nitropropionic acid

Grants and funding

This work was supported by a grant from a key project of the Chinese National Programs for Fundamental Research and Development (973 Program 2014CB138502). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.