The Impacts of Periconceptional Alcohol on Neonatal Ovaries and Subsequent Adult Fertility in the Rat.
Sarah E SteaneDanielle J BurgessKaren M MoritzLisa K AkisonPublished in: International journal of molecular sciences (2024)
Maternal exposures during pregnancy can impact the establishment of the ovarian reserve in offspring, the lifetime supply of germ cells that determine a woman's reproductive lifespan. However, despite alcohol consumption being common in women of reproductive age, the impact of prenatal alcohol on ovarian development is rarely investigated. This study used an established rat model of periconceptional ethanol exposure (PCEtOH; 12.5% v / v ethanol) for 4 days prior to 4 days post-conception. Ovaries were collected from neonates (day 3 and day 10), and genes with protein products involved in regulating the ovarian reserve analyzed by qPCR. Adult offspring had estrous cycles monitored and breeding performance assessed. PCEtOH resulted in subtle changes in expression of genes regulating apoptosis at postnatal day (PN) 3, whilst those involved in regulating growth and recruitment of primordial follicles were dysregulated at PN10 in neonatal ovaries. Despite these gene expression changes, there were no significant impacts on breeding performance in adulthood, nor on F2-generation growth or survival. This contributes additional evidence to suggest that a moderate level of alcohol consumption exclusively around conception, when a woman is often unaware of her pregnancy, does not substantially impact the fertility of her female offspring.
Keyphrases
- alcohol consumption
- gene expression
- cell cycle arrest
- high fat diet
- pregnancy outcomes
- childhood cancer
- oxidative stress
- induced apoptosis
- genome wide
- endoplasmic reticulum stress
- cell death
- poor prognosis
- pregnant women
- dna methylation
- preterm infants
- case report
- young adults
- polycystic ovary syndrome
- binding protein
- low birth weight
- pi k akt
- preterm birth
- high intensity
- body mass index
- cell proliferation
- transcription factor
- long non coding rna
- physical activity
- early life