Expression of GDAP1 gene correlates with alcohol deprivation effect

Alcohol addiction is a widespread disease, and the exact causes and consequences are still not fully determined. Neurotransmitters and neuronal circuits are not only the target structure of alcohol and responsible for its direct effects but also play a central role in the development of addiction. A gene that has been linked to alcohol use disorder in recent studies is the \(\textit {ganglioside-induced differentiation-associated protein 1 (GDAP1)}\) gene. The present study focuses on the hippocampus, a brain region particularly vulnerable to alcohol and rich in \(\it Gdap1\) gene expression. Using an established drinking model, alcohol drinking behavior was induced in adult male Long Evans rats. After 6 weeks of voluntary alcohol intake, followed by 2 weeks of deprivation, the animals were divided into two groups based on the alcohol deprivation effect (ADE). \(\it Gdap1\) gene expression was measured with real-time PCR in the hippocampus. Results reveal significantly decreased mRNA expression in the high ADE group compared to the low ADE group. This decrease was specifically detected within the cornu ammonis 3 (CA3) region. \(\it Gdap1\) expression in this region also negatively correlated with ADE in all animals. Taken together, results indicate that \(\it Gdap1\) might not only be associated with alcohol consumption but might even play a role in alcohol dependence.