Underlying Susceptibility to Eating Disorders and Drug Abuse: Genetic and Pharmacological Aspects of Dopamine D4 Receptors.
Luca BotticelliEmanuela Micioni Di BonaventuraFabio Del BelloGianfabio GiorgioniAlessandro PiergentiliAdele RomanoWilma QuagliaCarlo CifaniMaria Vittoria Micioni Di BonaventuraPublished in: Nutrients (2020)
The dopamine D4 receptor (DRD4) has a predominant expression in the prefrontal cortex (PFC), brain area strictly involved in the modulation of reward processes related to both food and drug consumption. Additionally, the human DRD4 gene is characterized by a variable number of tandem repeats (VNTR) in the exon 3 and, among the polymorphic variants, the 7-repeat (7R) allele appears as a contributing factor in the neurobiological mechanisms underlying drug abuse, aberrant eating behaviors and related comorbidities. The 7R variant encodes for a receptor with a blunted intracellular response to dopamine, and carriers of this polymorphism might be more tempted to enhance dopamine levels in the brain, through the overconsumption of drugs of abuse or palatable food, considering their reinforcing properties. Moreover, the presence of this polymorphism seems to increase the susceptibility of individuals to engage maladaptive eating patterns in response to negative environmental stimuli. This review is focused on the role of DRD4 and DRD4 genetic polymorphism in these neuropsychiatric disorders in both clinical and preclinical studies. However, further research is needed to better clarify the complex DRD4 role, by using validated preclinical models and novel compounds more selective for DRD4.
Keyphrases
- prefrontal cortex
- copy number
- genome wide
- physical activity
- white matter
- drug induced
- endothelial cells
- human health
- poor prognosis
- resting state
- uric acid
- intimate partner violence
- stem cells
- emergency department
- risk assessment
- gene expression
- dna methylation
- functional connectivity
- long non coding rna
- mesenchymal stem cells
- bone marrow
- pluripotent stem cells
- blood brain barrier