Gene-environment interactions resulting in risk alcohol drinking behaviour are mediated by CRF and CRF1.
- Authors
- Clarke, Toni-Kim; Schumann, Gunter
- Year
- 2009
- Journal
- Pharmacology, biochemistry, and behavior
- PMID
- 19409922
- DOI
- 10.1016/j.pbb.2009.04.014
Both genetic and environmental influences are known to influence an individuals' vulnerability to the misuse of alcohol. One of the most relevant environmental risk factors for alcoholism is that of stress. This review aims to examine the role of the biological stress systems in the etiology of alcoholism, with a focus on corticotrophin releasing factor (CRF) and its receptor CRF1. CRF is reviewed in the context of the biological stress systems within which it acts such as the HPA-axis, the noradrenergic system and the central and medial amygdale. These systems are examined in more detail by reviewing their genetic and molecular components in both humans and animals. It is concluded from the findings of the studies discussed in this review that CRF has a central role in the modulation of the stress response and that genetic variations in CRF or CRF1 may confer a susceptibility to alcoholism which is, in part, mediated by life stressors. Together these neurobiological, animal and human data suggest a role for CRF when developing treatment modalities for alcoholism alongside a pharmacogenetic approach to identify subtypes of patients which would benefit from these treatments or interventions.
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|---|---|---|---|---|
| Recent Efforts to Dissect the Genetic Basis of Alcohol Use and Abuse. | Sanchez-Roige S et al. | β | 2020 | β |
| Addictions Neuroclinical Assessment: A reverse translational approach. | Kwako LE et al. | β | 2017 | β |
| Late-Onset Cognitive Impairments after Early-Life Stress Are Shaped by Inherited Differences in Stress Reactivity. | McIlwrick S et al. | β | 2017 | β |
| Drug addiction: An affective-cognitive disorder in need of a cure. | Fattore L et al. | β | 2016 | β |
| Neurogenetics and gene therapy for reward deficiency syndrome: are we going to the Promised Land? | Blum K et al. | β | 2015 | β |
| Stress-response pathways are altered in the hippocampus of chronic alcoholics. | McClintick JN et al. | β | 2013 | β |
| The impact of self-reported life stress on current impulsivity in cocaine dependent adults. | Ross EL et al. | β | 2013 | β |
| Multiple polymorphisms in genes of the adrenergic stress system confer vulnerability to alcohol abuse. | Clarke TK et al. | β | 2012 | β |
| Serotonin transporter-linked polymorphic region (5-HTTLPR) genotype is associated with cortisol responsivity to naloxone challenge. | Stephens MA et al. | β | 2012 | β |
| Stress and the HPA axis: role of glucocorticoids in alcohol dependence. | Stephens MA et al. | β | 2012 | β |
| Drugs as instruments: a new framework for non-addictive psychoactive drug use. | MΓΌller CP et al. | β | 2011 | β |
| Molecular signaling and translational significance of the corticotropin releasing factor system. | Ronan PJ et al. | β | 2011 | β |
| Role of corticotropin-releasing factor in drug addiction: potential for pharmacological intervention. | Logrip ML et al. | β | 2011 | β |
| The influence of gene-environment interactions on alcohol consumption and alcohol use disorders: a comprehensive review. | Young-Wolff KC et al. | β | 2011 | β |
| The limbic-hypothalamic-pituitary-adrenal axis and the development of alcohol use disorders in youth. | Schepis TS et al. | β | 2011 | β |
| Consilient research approaches in studying gene x environment interactions in alcohol research. | Sher KJ et al. | β | 2010 | β |
| The role of oestradiol in sexually dimorphic hypothalamic-pituitary-adrena axis responses to intracerebroventricular ethanol administration in the rat. | Larkin JW et al. | β | 2010 | β |
| The genetics of alcoholism. | Stacey D et al. | β | 2009 | β |