Literature DB >> 28346058

Promising pharmacogenetic targets for treating alcohol use disorder: evidence from preclinical models.

Jennifer A Rinker1,2, Patrick J Mulholland1,2.   

Abstract

Inherited genetic variants contribute to risk factors for developing an alcohol use disorder, and polymorphisms may inform precision medicine strategies for treating alcohol addiction. Targeting genetic mutations linked to alcohol phenotypes has provided promising initial evidence for reducing relapse rates in alcoholics. Although successful in some studies, there are conflicting findings and the reports of adverse effects may ultimately limit their clinical utility, suggesting that novel pharmacogenetic targets are necessary to advance precision medicine approaches. Here, we describe promising novel genetic variants derived from preclinical models of alcohol consumption and dependence that may uncover disease mechanisms that drive uncontrolled drinking and identify novel pharmacogenetic targets that facilitate therapeutic intervention for the treatment of alcohol use disorder.

Entities:  

Keywords:  K+ channels; RAS signaling; alcohol use disorder; neuroimmune genes; pharmacogenetics; preclinical models; tachykinins

Mesh:

Substances:

Year:  2017        PMID: 28346058      PMCID: PMC5558539          DOI: 10.2217/pgs-2016-0193

Source DB:  PubMed          Journal:  Pharmacogenomics        ISSN: 1462-2416            Impact factor:   2.533


  155 in total

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  6 in total

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5.  Downregulation of M-channels in lateral habenula mediates hyperalgesia during alcohol withdrawal in rats.

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6.  Bioinformatics identification and pharmacological validation of Kcnn3/KCa2 channels as a mediator of negative affective behaviors and excessive alcohol drinking in mice.

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  6 in total

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