Exploration of Epigenetic State Hyperdopaminergia (Surfeit) and Genetic Trait Hypodopaminergia (Deficit) during Adolescent Brain Development

Author:

Blum Kenneth1,Bowirrat Abdalla2,Lewis Marjorie C.G.3,Simpatico Thomas A.4,Ceccanti Mauro5,Steinberg Bruce6,Modestino Edward J.6,Thanos Panayotis K.7,Baron David1,McLaughlin Thomas8,Brewer Raymond9,Badgaiyan Rajendra D.10,Ponce Jessica V.9,Lott Lisa9,Gold Mark S.11

Affiliation:

1. Division of Addiction Research and Education, Center for Psychiatry, Medicine, Primary Care (Office of Provost), Western University Health Sciences, Pomona, CA, United States

2. Department of Molecular Biology and Adelson School of Medicine, Ariel University, Ariel, Israel

3. Departments of Anatomy & Psychiatry & Behavioural Sciences, Howard University School of Medicine, Washington, DC, United States

4. Department of Psychiatry, University of Vermont, School of Medicine, Burlington, VA, United States

5. Department of Translational and Precision Medicine, Sapienza University, Rome, Italy

6. Department of Psychology, Curry College, Milton, MA, United States

7. Institute of Addiction Research, NY, United States

8. Center for Psychiatric Medicine, Lawrence, MA, United States

9. Division of Precision Addiction Management, Geneus Health, LLC., San Antonio, TX, United States

10. Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, Long School of Medicine, University of Texas Medical Center, San Antonio, TX, United States

11. Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, United States

Abstract

Background: The risk for all addictive drug and non-drug behaviors, especially, in the unmyelinated Prefrontal Cortex (PFC) of adolescents, is important and complex. Many animal and human studies show the epigenetic impact on the developing brain in adolescents, compared to adults. Some reveal an underlying hyperdopaminergia that seems to set our youth up for risky behaviors by inducing high quanta pre-synaptic dopamine release at reward site neurons. In addition, altered reward gene expression in adolescents caused epigenetically by social defeat, like bullying, can continue into adulthood. In contrast, there is also evidence that epigenetic events can elicit adolescent hypodopaminergia. This complexity suggests that neuroscience cannot make a definitive claim that all adolescents carry a hyperdopaminergia trait. Objective: The primary issue involves the question of whether there exists a mixed hypo or hyper - dopaminergia in this population. Methods: Genetic Addiction Risk Score (GARS®) testing was carried out of 24 Caucasians of ages 12-19, derived from families with RDS. Results: We have found that adolescents from this cohort, derived from RDS parents, displayed a high risk for any addictive behavior (a hypodopaminergia), especially, drug-seeking (95%) and alcohol- seeking (64%). Conclusion: The adolescents in our study, although more work is required, show a hypodopaminergic trait, derived from a family with Reward Deficiency Syndrome (RDS). Certainly, in future studies, we will analyze GARS in non-RDS Caucasians between the ages of 12-19. The suggestion is first to identify risk alleles with the GARS test and, then, use well-researched precision, pro-dopamine neutraceutical regulation. This “two-hit” approach might prevent tragic fatalities among adolescents, in the face of the American opioid/psychostimulant epidemic.

Funder

National Institutes of Health

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmacology (medical),Psychiatry and Mental health,Pharmacology

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