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Medications are typically administered to achieve therapeutic effects. Some drugs can modify an individual's mood and perception, frequently resulting in various enjoyable experiences. However, this can result in drug dependency, a condition marked by continuous drug use despite potential negative consequences. Drug dependency primarily falls into two categories: psychological and physical dependence. Psychological dependence occurs when the pleasurable feelings induced by the drug...
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Disruption of Frontal Lobe Neural Synchrony During Cognitive Control by Alcohol Intoxication
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Reprogramming of mPFC transcriptome and function in alcohol dependence.

M Heilig1, E Barbier1, A L Johnstone2

  • 1Center for Social and Affective Neuroscience, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.

Genes, Brain, and Behavior
|September 23, 2016
PubMed
Summary
This summary is machine-generated.

Alcohol dependence causes brain changes in the medial prefrontal cortex (mPFC), leading to compulsive drinking. Epigenetic modifications, like DNA hypermethylation, reprogram mPFC function, driving addiction behaviors.

Keywords:
Alcohol use disorderBDNFDNA methylationanimal modelinhibitory controlmGlur2miRNAneuronal ensemblepost-dependenttranscriptomeviral vector

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Area of Science:

  • Neuroscience
  • Molecular Biology
  • Addiction Research

Background:

  • Alcohol dependence involves neuroadaptations promoting compulsive alcohol seeking and intake.
  • The medial prefrontal cortex (mPFC) regulates behaviors related to alcohol consumption.
  • Repeated alcohol intoxication and withdrawal cycles induce lasting changes in brain function.

Purpose of the Study:

  • To review emerging literature on mPFC functional reprogramming in alcohol dependence.
  • To highlight molecular dysregulations contributing to the post-dependent syndrome.
  • To identify epigenetic mechanisms driving long-term alcohol-related behaviors.

Main Methods:

  • Review of existing scientific literature on alcohol dependence and mPFC function.
  • Analysis of studies investigating molecular signaling pathways (glutamatergic, BDNF, calcium homeostasis).
  • Examination of epigenetic modifications, including DNA hypermethylation and histone modifications.

Main Results:

  • Prolonged alcohol exposure reprograms mPFC function, contributing to addiction.
  • Altered glutamatergic and BDNF signaling, calcium homeostasis, and neurotransmitter release are implicated.
  • Global DNA hypermethylation and repression of histone modifying enzymes, like PRDM2, are key epigenetic changes.
  • These epigenetic changes drive molecular and behavioral consequences of alcohol dependence.

Conclusions:

  • Epigenetic alterations in the mPFC are crucial for the development of alcoholism.
  • Targeting these epigenetic modifications offers potential for novel disease-modifying treatments for alcohol dependence.