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Series GSE212651 Query DataSets for GSE212651
Status Public on Aug 30, 2023
Title Abstinence from Escalation of Cocaine Intake Changes the microRNA Landscape in the Cortico-Accumbal Pathway
Organism Rattus norvegicus
Experiment type Non-coding RNA profiling by high throughput sequencing
Summary Cocaine administration alters the microRNA (miRNA) landscape in the cortico-accumbal pathway. These changes in miRNA can play a major role in the posttranscriptional regulation of gene expression during withdrawal. This study aimed to investigate the changes in microRNA expression in the cortico-accumbal pathway during acute withdrawal and protracted abstinence following escalated cocaine intake. Small RNA sequencing (sRNA-seq) was used to profile miRNA
transcriptomic changes in the cortico-accumbal pathway [infralimbic- and prelimbic-prefrontal cortex (IL and PL) and nucleus accumbens (NAc)] of rats with extended access to cocaine self-administration followed by an 18-h withdrawal or a 4-week abstinence. An 18-h withdrawal led to differential expression (fold-change > 1.5 and p < 0.05) of 21 miRNAs in the IL, 18 miRNAs in the PL, and two miRNAs in the NAc. The mRNAs potentially targeted by these miRNAs were enriched in the following pathways: gap junctions, neurotrophin signaling, MAPK signaling, and cocaine addiction. Moreover, a 4-week abstinence led to differential expression (fold-change > 1.5 and p < 0.05) of 23 miRNAs in the IL, seven in the PL, and five miRNAs in the NAc. The mRNAs potentially targeted by these miRNAs were enriched in pathways including gap junctions, cocaine addiction, MAPK signaling,
glutamatergic synapse, morphine addiction, and amphetamine addiction. Additionally, the expression levels of several miRNAs differentially expressed in either the IL or the NAc were significantly correlated with addiction behaviors. Our findings highlight the impact of acute and protracted abstinence from escalated cocaine intake on miRNA expression in the cortico-accumbal pathway, a key circuit in addiction, and suggest developing novel biomarkers and therapeutic approaches to prevent relapse by targeting abstinence-associated miRNAs and their regulated mRNAs.
 
Overall design Compare miRNA transcriptome profiles among the three groups of rats (4-week abstinence vs. naïve; 16-hr withdrawal vs. naïve; and 4-week abstinence vs. 16-hr withdrawal)
 
Contributor(s) Huiping Z
Citation(s) 37239038
NIH grant(s)
Grant ID Grant title Affiliation Name
R01 AA025080 Brain microRNA-mRNA regulatory networks and alcohol use disorders BOSTON UNIVERSITY Huiping Zhang
R01 AA029758 Identifying Brain Epitranscriptomic Changes Associated with Alcohol Use Disorder BOSTON UNIVERSITY Huiping Zhang
U01 DA043799 Identification of Genetic Variants that Contribute to Compulsive Cocaine Intakein Rats THE REGENTS OF THE UNIV. OF CALIF., UNIV. OF CALIF., SAN DIEGO Olivier George
Submission date Sep 03, 2022
Last update date Aug 30, 2023
Contact name Huiping Zhang
E-mail(s) huipingz@bu.edu
Organization name Boston University
Street address 72 East Concord Street
City Boston
State/province MA
ZIP/Postal code 02118
Country USA
 
Platforms (1)
GPL18694 Illumina HiSeq 2500 (Rattus norvegicus)
Samples (36)
GSM6542416 HZ_1
GSM6542417 HZ_2
GSM6542418 HZ_3
Relations
BioProject PRJNA876564

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE212651_Raw_gene_counts_matrix.txt.gz 36.5 Kb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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