Retrieved from https://www.eurekalert.org/news-releases/1131296
A growing body of research suggests that a father’s health before conception may play a larger role in child development than previously understood — and researchers are working to understand how a father’s drinking before conception may affect offspring health and development.
Dr. Michael Golding, a professor in the Texas A&M College of Veterinary Medicine and Biomedical Sciences Department of Veterinary Physiology and Pharmacology, studies how alcohol exposure may alter biological signals in sperm in ways that affect offspring development and metabolism.
Through a new $2.9 million grant from the National Institute on Alcohol Abuse and Alcoholism (NIAAA), part of the National Institutes of Health (NIH), and supported by Texas A&M AgriLife Research, Golding and his team will expand their research into how parental alcohol exposure may contribute to chronic disease, accelerated aging and developmental disorders in offspring.
“We want to understand how the memory of paternal alcohol exposure transmits to the children and then how it predisposes them to birth defects and chronic disease later in life,” Golding said.
Expanding research on alcohol exposure and chronic disease
The study builds on Golding’s previous research exploring how paternal alcohol exposure contributes to fetal growth restriction and birth defects.
“In this phase, we want to see if dad’s drinking interacts with mom’s drinking to make things worse,” Golding said. “Do these things compound and contribute to worse health outcomes over time for their children?”
A major focus of the project is the mitochondria — the parts of cells responsible for producing energy. Golding’s team believes alcohol-related stress (stress that impacts the body on a cellular level) alters important molecular signals in sperm, disrupting mitochondrial function in offspring and potentially accelerating aging and disease development.
Golding and his team are studying how a father’s alcohol use can alter the biological information passed to his children — without changing their DNA — with the goal of one day finding ways to improve outcomes for those impacted by FASD.
“If your dysfunctional mitochondria represent a flat tire, you’re basically starting off life with a flat tire,” Golding said. “The question is, ‘how far do you get before the car starts to break down?’”