NRF2 attenuation aggravates detrimental consequences of metabolic stress on cultured porcine parthenote embryos
View abstract on PubMed
Summary
This summary is machine-generated.Nuclear factor erythroid 2-related factor 2 (NRF2) is vital for early embryo development. Attenuating NRF2 impairs blastocyst formation, especially under high glucose conditions, but melatonin may offer some protection.
Area Of Science
- Reproductive Biology
- Molecular Biology
- Developmental Biology
Background
- Nuclear factor erythroid 2-related factor 2 (NRF2) regulates oxidative stress responses.
- NRF2's role in early embryonic development is not well understood.
- NRF2 binds antioxidant response elements to control gene expression.
Purpose Of The Study
- To investigate the expression and function of NRF2 during porcine early embryo development.
- To determine the impact of NRF2 attenuation on embryo development under varying glucose concentrations.
- To assess the potential protective effect of melatonin on NRF2-deficient embryos.
Main Methods
- NRF2 mRNA expression analysis in porcine embryos (day 2-7).
- Assessment of parthenogenetic embryo development after NRF2 mRNA attenuation.
- Culture of NRF2-attenuated embryos under different glucose and melatonin conditions.
Main Results
- NRF2 mRNA is present throughout porcine early development, with dynamic changes in abundance.
- NRF2 attenuation significantly reduced blastocyst development rates.
- High glucose concentrations exacerbated the negative effects of NRF2 attenuation on embryo development.
- Melatonin partially rescued development in NRF2-attenuated embryos under moderate glucose stress.
Conclusions
- NRF2 plays a critical role in early porcine embryo development.
- NRF2 is essential for mitigating metabolic stress during embryonic development.
- Targeting NRF2 pathways or using antioxidants like melatonin may improve embryo viability under stress.

