MicroRNAs in drug addiction: Current status and future perspectives

Elsevier

Available online 21 May 2022, 108215

Pharmacology & TherapeuticsAbstract

Drug addiction is a chronic and relapsing brain disorder characterized by compulsive drug seeking and continued drug use despite adverse consequences. The high prevalence and social burden of addiction is indisputable; however, the available intervention is insufficient. Abnormal gene expression is observed in reward-related brain regions in animal models of addiction. The modulation of gene expression and aberrant adaptation of neural networks attribute to the changes in brain function under repeated exposure to addictive drugs. The emerging recognition of the role of microRNA (miRNA) provides new insights into many biological and pathological processes in the central nervous system. Considerable studies have demonstrated that miRNAs are strong modulators of posttranscriptional gene expression in drug addiction. Here, we provide an overview of miRNAs, followed by evidence for aberrant miRNA expression and regulatory roles of miRNAs in drug addiction as well as neuroadaptation. We concluded by providing our perspectives that miRNAs have the potential as novel therapeutic targets for drug addiction.

Keywords

microRNAs (miRNAs)

Drug addiction

Neuroadaptation

Biomarker

AbbreviationsAgo2

argonaute RISC catalytic component 2

AT1R

Angiotensin II type 1 receptor

BDNF

brain-derived neurotrophic factor

BK channel

large-conductance Ca2+ and voltage-activated K+ channel

CNS

central nervous system

CREB

cAMP response element-binding

DNMT

DNA methyltransferases

EAAT

excitatory amino acid transporter

GABAA

γ-aminobutyric acid receptor A

HDAC5

histone deacetylase 5

MeCP2

methyl CpG binding protein 2

NMDA

N-methyl-D-aspartic acid receptor

NeuroD

neurogenic differentiation 1

REST

repressor element silencing transcription factor

RISC

RNA-induced silencing complex

RT–PCR

reverse transcription-polymerase–chain reaction

TrkB

tropomyosin-related kinase B

VTA

ventral tegmental area.

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© 2022 Published by Elsevier Inc.

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