The overall objective of the proposed research is to enhance understanding of the relationship between biological and psychosocial risk and protective factors and level of alcohol involvement (alcohol use and alcohol-related problems) in Mexican American young adults. This project will be an extension of our previous investigations that have evaluated vulnerability factors associated with alcohol involvement in young adult Native Americans, African Americans, Asian Americans, and EuroAmericans living in San Diego, CA. Hispanics are the second largest ethnic minority group in the U.S. and the largest in the city of San Diego, yet biopsychosocial vulnerability factors for alcohol problems in this population remain relatively unexplored. We now have preliminary data that suggests a distinct cluster of biological factors may be associated with alcohol involvement in Mexican American young adults that merit further investigation. These potential biological vulnerability factors include: the presence of certain EEG variants previously associated with alcoholism risk in EuroAmericans, a quantitatively different response to alcohol challenge (see Polich Component), and a distribution of alcohol metabolizing genotypes (ADH2*3 and CYP2E 1 alleles). New studies utilizing EEG and ERP paradigms are proposed. A longitudinal follow-up is planned. This study will assess drinking patterns, alcohol-related problems, and psychiatric diagnoses, and is designed in a manner suitable for the development of a study that can eventually incorporate genetic analyses. Select psychosocial variables will be assessed and a risk/protective factor model will be developed and tested (see Clinical Core). Additionally, a new set of measures that index vulnerability and neuroadaption to alcohol will be developed that may allow parallel investigations to be made in human participants and animal models within the center. Ultimately, a better understanding of the factors associated with alcohol behavior in Mexican Americans will contribute important information for understanding the causes of alcohol abuse and dependence and might aid in the development of efficacious and culturally sensitive prevention and intervention programs.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Comprehensive Center (P60)
Project #
5P60AA006420-22
Application #
7552588
Study Section
Project Start
Project End
Budget Start
2005-01-01
Budget End
2005-12-31
Support Year
22
Fiscal Year
2005
Total Cost
$281,550
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
781613492
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Spierling, Samantha R; Kreisler, Alison D; Williams, Casey A et al. (2018) Intermittent, extended access to preferred food leads to escalated food reinforcement and cyclic whole-body metabolism in rats: Sex differences and individual vulnerability. Physiol Behav 192:3-16
Blasio, Angelo; Wang, Jingyi; Wang, Dan et al. (2018) Novel Small-Molecule Inhibitors of Protein Kinase C Epsilon Reduce Ethanol Consumption in Mice. Biol Psychiatry 84:193-201
Kirson, Dean; Oleata, Christopher Shaun; Parsons, Loren Howell et al. (2018) CB1 and ethanol effects on glutamatergic transmission in the central amygdala of male and female msP and Wistar rats. Addict Biol 23:676-688
Matzeu, Alessandra; Kallupi, Marsida; George, Olivier et al. (2018) Dynorphin Counteracts Orexin in the Paraventricular Nucleus of the Thalamus: Cellular and Behavioral Evidence. Neuropsychopharmacology 43:1010-1020
de Guglielmo, Giordano; Conlisk, Dana E; Barkley-Levenson, Amanda M et al. (2018) Inhibition of Glyoxalase 1 reduces alcohol self-administration in dependent and nondependent rats. Pharmacol Biochem Behav 167:36-41
Matzeu, Alessandra; Terenius, Lars; Martin-Fardon, Remi (2018) Exploring Sex Differences in the Attenuation of Ethanol Drinking by Naltrexone in Dependent Rats During Early and Protracted Abstinence. Alcohol Clin Exp Res 42:2466-2478
Kononoff, Jenni; Melas, Philippe A; Kallupi, Marsida et al. (2018) Adolescent cannabinoid exposure induces irritability-like behavior and cocaine cross-sensitization without affecting the escalation of cocaine self-administration in adulthood. Sci Rep 8:13893
Verheij, Michel M M; Contet, Candice; Karel, Peter et al. (2018) Median and Dorsal Raphe Serotonergic Neurons Control Moderate Versus Compulsive Cocaine Intake. Biol Psychiatry 83:1024-1035
Schmeichel, Brooke E; Matzeu, Alessandra; Koebel, Pascale et al. (2018) Knockdown of hypocretin attenuates extended access of cocaine self-administration in rats. Neuropsychopharmacology 43:2373-2382
Kononoff, Jenni; Kallupi, Marsida; Kimbrough, Adam et al. (2018) Systemic and Intra-Habenular Activation of the Orphan G Protein-Coupled Receptor GPR139 Decreases Compulsive-Like Alcohol Drinking and Hyperalgesia in Alcohol-Dependent Rats. eNeuro 5:

Showing the most recent 10 out of 211 publications