Abstract

In preeclampsia, it is believed that widespread endothelial dysfunction leads to reduced placental perfusion and increased oxidative stress. Oxidative stress is the accumulation of reactive oxygen species (ROS) such as superoxide (O2-), nitric oxide (NO), and peroxynitrite (ONOO-). Our lab has previously established a colony of transgenic mice that do not express catechol-O-methyl transferase (COMT-/-). COMT produces 2-methoxyestradiol (2-ME), a potent vasodilator that is normally increased in pregnancy. Pregnant COMT-/- mice exhibit a phenotype similar to the one observed in preeclampsia. We hypothesize that COMT-/- mice have a decreased tolerance to prenatal hypoxic insults, characterized by an increase in placental oxidative stress when compared to control (C57) mice exposed to similar conditions.

Highlights

  • In preeclampsia, it is believed that widespread endothelial dysfunction leads to reduced placental perfusion and increased oxidative stress

  • We hypothesize that COMT-/- mice have a decreased tolerance to prenatal hypoxic insults, characterized by an increase in placental oxidative stress when compared to control (C57) mice exposed to similar conditions

  • No significant differences in placental levels of superoxide were observed among experimental groups

Read more

Summary

Introduction

It is believed that widespread endothelial dysfunction leads to reduced placental perfusion and increased oxidative stress. Oxidative stress is the accumulation of reactive oxygen species (ROS) such as superoxide (O2-), nitric oxide (NO), and peroxynitrite (ONOO-). Our lab has previously established a colony of transgenic mice that do not express catechol-Omethyl transferase (COMT-/-). COMT produces 2methoxyestradiol (2-ME), a potent vasodilator that is normally increased in pregnancy. Pregnant COMT-/mice exhibit a phenotype similar to the one observed in preeclampsia. We hypothesize that COMT-/- mice have a decreased tolerance to prenatal hypoxic insults, characterized by an increase in placental oxidative stress when compared to control (C57) mice exposed to similar conditions

Methods
Results
Conclusions
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.