
Targeting Epigenetic Mechanisms to Treat Alcohol Use Disorders (AUD)
Author(s) -
Fernando Mateos Rodríguez
Publication year - 2021
Publication title -
current pharmaceutical design
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.69
H-Index - 159
eISSN - 1873-4286
pISSN - 1381-6128
DOI - 10.2174/1381612827666210203142539
Subject(s) - alcohol use disorder , medicine , epigenetics , disease , psychiatry , bioinformatics , alcohol , biology , genetics , pathology , biochemistry , gene
Background: The impact of abusive alcohol consumption on human health is remarkable. Accordingto the World Health Organization (WHO), approximately 3.3 million people die annually because of harmfulalcohol consumption (the figure represents around 5.9% of global deaths). Alcohol Use Disorder (AUD) is achronic disease where individuals exhibit compulsive alcohol drinking and present negative emotional stateswhen they do not drink. In the most severe manifestations of AUD, the individuals lose control over intake despitea decided will to stop drinking. Given the multiple faces and the specific forms of this disease, the termAUD often appears in the plural (AUDs). Since only a few approved pharmacological treatments are availableto treat AUD and they do not apply to all individuals or AUD forms, the search for compounds that may help toeliminate the burden of the disease and complement other therapeutical approaches is necessary. Method: This work reviews recent research focused on the involvement of epigenetic mechanisms in the pathophysiologyof AUD. Excessive drinking leads to chronic and compulsive consumption that eventually damagesthe organism. The central nervous system is a key target and is the focus of this study. The search for the geneticand epigenetic mechanisms behind the intricated dysregulation induced by ethanol will aid researchers inestablishing new therapy approaches. Conclusion: Recent findings in the field of epigenetics are essential and offer new windows for observation and research.The study of small molecules that inhibit key epienzymes involved in nucleosome architecture dynamics is necessary inorder to prove their action and specificity in the laboratory and to test their effectivity and safety in clinical trials withselected patients bearing defined alterations caused by ethanol.