Drug addiction is a psychiatric disorder characterized by a transition from recreational to compulsive drug use that continues in spite of severe negative consequences. Despite attempts by individuals to quit, the desire or need to resume drug-taking can last for months or years. The persistence of addiction over time suggests that exposure to drugs results in long-term adaptations in the brain that likely involve alterations in transcription and genetic regulation. In addition to genetic factors, epigenetic mechanisms may also play a role in the maintenance of addictions not only throughout an individual's lifetime, but in his/her descendants. However, the potential impact of drug exposure across generations has not been characterized. To date, no comprehensive study has been undertaken to determine if exposure to drugs of abuse in the parental generation leads to alterations in behavioral or molecular phenotypes in subsequent generations. To address this question, we will examine the phenotypic consequences of two mechanistically different drugs (cocaine and morphine) in three inbred mouse strains (C57BL/6J, DBA/2J, A/J) as well as a multi-generation series of F1 hybrids. In addition to studying behavioral phenotypes across generations, we will characterize RNA expression, DNA methylation, and post-translational histone modifications as both the molecular signature and the mechanistic basis for heritable epigenetic changes. These studies will allow us to determine (1) whether any of 2 mechanistically different drugs of abuse results in transmission of addiction-related phenotypes through multiple generations after treatment, (2) whether these phenotypes are mediated by changes to the epigenome (DNA methylation, post-translational histone modifications, or RNAs), and (3) whether these phenotypes vary according to the sex of exposed parent in an imprinted or allele-specific manner. These experiments will inform future studies aimed at elucidating the mechanisms by which drugs of abuse lead to transgenerational phenotypes.
The inheritance of many psychiatric diseases, such as addiction, is evident in the population. However despite the millions of dollars spent on genome-wide association studies, the genetic variance in risk for most addictions has eluded discovery. The fact that not all inherited information is present in the DNA sequence and that """"""""epigenetic"""""""" information in the form of chemical modifications of DNA can be passed from parent to offspring is just now being appreciated. Techniques are available to identify these variants in a high-throughput fashion;however it is critical to establish first if epigenetically inherited variation contributes to addiction. The mouse has been used extensively in both behavioral pharmacology as well as genetic studies to investigate mechanisms underlying addiction, thus it is a tractable organism with which to detect epigenetic inheritance. These discoveries could revolutionize our understanding of inherited risk for drug abuse and in doing so change behavior of future generations.
|Browne, Caroline A; Erickson, Rebecca L; Blendy, Julie A et al. (2017) Genetic variation in the behavioral effects of buprenorphine in female mice derived from a murine model of the OPRM1 A118G polymorphism. Neuropharmacology 117:401-407|
|Yohn, Nicole L; Blendy, Julie A (2017) Adolescent Chronic Unpredictable Stress Exposure Is a Sensitive Window for Long-Term Changes in Adult Behavior in Mice. Neuropsychopharmacology 42:1670-1678|
|Yohn, Nicole L; Bartolomei, Marisa S; Blendy, Julie A (2015) Multigenerational and transgenerational inheritance of drug exposure: The effects of alcohol, opiates, cocaine, marijuana, and nicotine. Prog Biophys Mol Biol 118:21-33|
|Buchner, David A; Nadeau, Joseph H (2015) Contrasting genetic architectures in different mouse reference populations used for studying complex traits. Genome Res 25:775-91|
|Briand, Lisa A; Hilario, Monica; Dow, Holly C et al. (2015) Mouse model of OPRM1 (A118G) polymorphism increases sociability and dominance and confers resilience to social defeat. J Neurosci 35:3582-90|