TY - JOUR
T1 - Sex, Drugs, and Rock 'N' Roll
T2 - Hypothesizing common mesolimbic activation as a function of reward gene polymorphisms
AU - Blum, Kenneth
AU - Werner, Tonia
AU - Carnes, Stefanie
AU - Carnes, Patrick
AU - Bowirrat, Abdalla
AU - Giordano, John
AU - Berman, Marlene Oscar
AU - Gold, Mark
N1 - Funding Information:
The authors are indebted to the superb editorial work by Margaret Madigan and Paula J. Edge. The writing of this paper was supported in part by funds from the US Department of Health Services, NIAAA (R01-AA07112 and K05-AA00219) and the Medical Research Service of the US Department of Veterans Affairs (Marlene Oscar-Berman). Conflict of interest: Kenneth Blum, PhD owns stock in LifeGen, Inc. San Diego, CA, a neurogentics company involved in developing natural DA D2 agonists and genetic testing.
PY - 2012
Y1 - 2012
N2 - The nucleus accumbens, a site within the ventral striatum, plays a prominent role in mediating the reinforcing effects of drugs of abuse, food, sex, and other addictions. Indeed, it is generally believed that this structure mandates motivated behaviors such as eating, drinking, and sexual activity, which are elicited by natural rewards and other strong incentive stimuli. This article focuses on sex addiction, but we hypothesize that there is a common underlying mechanism of action for the powerful effects that all addictions have on human motivation. That is, biological drives may have common molecular genetic antecedents, which if impaired, lead to aberrant behaviors. Based on abundant scientific support, we further hypothesize that dopaminergic genes, and possibly other candidate neurotransmitter-related gene polymorphisms, affect both hedonic and anhedonic behavioral outcomes. Genotyping studies already have linked gene polymorphic associations with alcohol and drug addictions and obesity, and we anticipate that future genotyping studies of sex addicts will provide evidence for polymorphic associations with specific clustering of sexual typologies based on clinical instrument assessments. We recommend that scientists and clinicians embark on research coupling the use of neuroimaging tools with dopaminergic agonistic agents to target specific gene polymorphisms systematically for normalizing hyper- or hypo-sexual behaviors.
AB - The nucleus accumbens, a site within the ventral striatum, plays a prominent role in mediating the reinforcing effects of drugs of abuse, food, sex, and other addictions. Indeed, it is generally believed that this structure mandates motivated behaviors such as eating, drinking, and sexual activity, which are elicited by natural rewards and other strong incentive stimuli. This article focuses on sex addiction, but we hypothesize that there is a common underlying mechanism of action for the powerful effects that all addictions have on human motivation. That is, biological drives may have common molecular genetic antecedents, which if impaired, lead to aberrant behaviors. Based on abundant scientific support, we further hypothesize that dopaminergic genes, and possibly other candidate neurotransmitter-related gene polymorphisms, affect both hedonic and anhedonic behavioral outcomes. Genotyping studies already have linked gene polymorphic associations with alcohol and drug addictions and obesity, and we anticipate that future genotyping studies of sex addicts will provide evidence for polymorphic associations with specific clustering of sexual typologies based on clinical instrument assessments. We recommend that scientists and clinicians embark on research coupling the use of neuroimaging tools with dopaminergic agonistic agents to target specific gene polymorphisms systematically for normalizing hyper- or hypo-sexual behaviors.
KW - Dopamine
KW - Mesolimbic systems
KW - Neurogenetics
KW - Reward deficiency syndrome (RDS)
KW - Sexual addiction
UR - http://www.scopus.com/inward/record.url?scp=84862588560&partnerID=8YFLogxK
U2 - 10.1080/02791072.2012.662112
DO - 10.1080/02791072.2012.662112
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C2 - 22641964
AN - SCOPUS:84862588560
SN - 0279-1072
VL - 44
SP - 38
EP - 55
JO - Journal of Psychoactive Drugs
JF - Journal of Psychoactive Drugs
IS - 1
ER -