Early Life Stress, Nicotinic Acetylcholine Receptors and Alcohol Use Disorders

Stress is a major driving force in alcohol use disorders (AUDs). It influences how much one consumes, craving intensity and whether an abstinent individual will return to harmful alcohol consumption. We are most vulnerable to the effects of stress during early development, and exposure to multiple t...

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Main Authors: Joan Y. Holgate, Selena E. Bartlett
Format: Article
Language:English
Published: MDPI AG 2015-06-01
Series:Brain Sciences
Subjects:
Online Access:http://www.mdpi.com/2076-3425/5/3/258
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spelling doaj-ec527de39706406fab5511baf377d6f92020-11-25T01:02:52ZengMDPI AGBrain Sciences2076-34252015-06-015325827410.3390/brainsci5030258brainsci5030258Early Life Stress, Nicotinic Acetylcholine Receptors and Alcohol Use DisordersJoan Y. Holgate0Selena E. Bartlett1Institute of Health and Biomedical Innovation, Translational Research Institute, Queensland University of Technology, 37 Kent St, Woolloongabba, Queensland 4102, AustraliaInstitute of Health and Biomedical Innovation, Translational Research Institute, Queensland University of Technology, 37 Kent St, Woolloongabba, Queensland 4102, AustraliaStress is a major driving force in alcohol use disorders (AUDs). It influences how much one consumes, craving intensity and whether an abstinent individual will return to harmful alcohol consumption. We are most vulnerable to the effects of stress during early development, and exposure to multiple traumatic early life events dramatically increases the risk for AUDs. However, not everyone exposed to early life stress will develop an AUD. The mechanisms determining whether an individual’s brain adapts and becomes resilient to the effects of stress or succumbs and is unable to cope with stress remain elusive. Emerging evidence suggests that neuroplastic changes in the nucleus accumbens (NAc) following early life stress underlie the development of AUDs. This review discusses the impact of early life stress on NAc structure and function, how these changes affect cholinergic signaling within the mesolimbic reward pathway and the role nicotinic acetylcholine receptors (nAChRs) play in this process. Understanding the neural pathways and mechanism determining stress resilience or susceptibility will improve our ability to identify individuals susceptible to developing AUDs, formulate cognitive interventions to prevent AUDs in susceptible individuals and to elucidate and enhance potential therapeutic targets, such as the nAChRs, for those struggling to overcome an AUD.http://www.mdpi.com/2076-3425/5/3/258Early life stressalcoholnicotinic acetylcholine receptorsstress resiliencenucleus accumbenscholinergicmesolimbicdopamineGABA
collection DOAJ
language English
format Article
sources DOAJ
author Joan Y. Holgate
Selena E. Bartlett
spellingShingle Joan Y. Holgate
Selena E. Bartlett
Early Life Stress, Nicotinic Acetylcholine Receptors and Alcohol Use Disorders
Brain Sciences
Early life stress
alcohol
nicotinic acetylcholine receptors
stress resilience
nucleus accumbens
cholinergic
mesolimbic
dopamine
GABA
author_facet Joan Y. Holgate
Selena E. Bartlett
author_sort Joan Y. Holgate
title Early Life Stress, Nicotinic Acetylcholine Receptors and Alcohol Use Disorders
title_short Early Life Stress, Nicotinic Acetylcholine Receptors and Alcohol Use Disorders
title_full Early Life Stress, Nicotinic Acetylcholine Receptors and Alcohol Use Disorders
title_fullStr Early Life Stress, Nicotinic Acetylcholine Receptors and Alcohol Use Disorders
title_full_unstemmed Early Life Stress, Nicotinic Acetylcholine Receptors and Alcohol Use Disorders
title_sort early life stress, nicotinic acetylcholine receptors and alcohol use disorders
publisher MDPI AG
series Brain Sciences
issn 2076-3425
publishDate 2015-06-01
description Stress is a major driving force in alcohol use disorders (AUDs). It influences how much one consumes, craving intensity and whether an abstinent individual will return to harmful alcohol consumption. We are most vulnerable to the effects of stress during early development, and exposure to multiple traumatic early life events dramatically increases the risk for AUDs. However, not everyone exposed to early life stress will develop an AUD. The mechanisms determining whether an individual’s brain adapts and becomes resilient to the effects of stress or succumbs and is unable to cope with stress remain elusive. Emerging evidence suggests that neuroplastic changes in the nucleus accumbens (NAc) following early life stress underlie the development of AUDs. This review discusses the impact of early life stress on NAc structure and function, how these changes affect cholinergic signaling within the mesolimbic reward pathway and the role nicotinic acetylcholine receptors (nAChRs) play in this process. Understanding the neural pathways and mechanism determining stress resilience or susceptibility will improve our ability to identify individuals susceptible to developing AUDs, formulate cognitive interventions to prevent AUDs in susceptible individuals and to elucidate and enhance potential therapeutic targets, such as the nAChRs, for those struggling to overcome an AUD.
topic Early life stress
alcohol
nicotinic acetylcholine receptors
stress resilience
nucleus accumbens
cholinergic
mesolimbic
dopamine
GABA
url http://www.mdpi.com/2076-3425/5/3/258
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