Transcriptional response to chronic long-access fentanyl self-administration in rat habenula and amygdala.
Ontology highlight
ABSTRACT: Fentanyl is a potent synthetic opioid associated with overdose. However, little is known about fentanyl-induced molecular adaptations in the habenula and amygdala, two brain regions implicated in opioid use and withdrawal. We performed bulk RNA-sequencing in the rat habenula and amygdala to identify transcriptomic changes associated with fentanyl intake. Rats self-administered intravenous saline or fentanyl over 22-24 days. Ninety minutes following the final session, brains were collected for transcriptomic profiling. In Hb, we identified 453 differentially expressed genes (DEGs) between saline and fentanyl rats, with upregulated genes associated with synaptic transmission and ionic conductance. In amygdala, we identified 3,041 fentanyl-associated DEGs with upregulated genes implicated in
SUBMITTER: Magnard R
PROVIDER: S-EPMC12699572 | biostudies-literature | 2025 Dec
REPOSITORIES: biostudies-literature
ACCESS DATA