Sleep and circadian rhythm activity alterations during adolescence in a mouse model of neonatal fentanyl withdrawal syndrome
- PMID: 39914521
- PMCID: PMC11884988
- DOI: 10.1016/j.neuroscience.2025.01.064
Sleep and circadian rhythm activity alterations during adolescence in a mouse model of neonatal fentanyl withdrawal syndrome
Abstract
Fentanyl, a highly potent synthetic opioid, is a major contributor to the ongoing opioid epidemic. During adulthood, fentanyl is known to induce pronounced sleep and circadian disturbances during use and withdrawal. Children exposed to opioids in utero are likely to develop neonatal opioid withdrawal syndrome, and display sleep disturbances after birth. However, it is currently unknown how neonatal opioid withdrawal from fentanyl impacts sleep and circadian rhythms in mice later in life. To model neonatal opioid withdrawal syndrome, mice were treated with fentanyl from postnatal days 1 through 14, analogous to the third trimester of human gestation. After weaning, fentanyl and saline treated mice underwent non-invasive sleep and circadian rhythm monitoring during adolescence postnatal days 23 through 30. Neonatal fentanyl exposure led to an increase in the percent time spent in rapid eye movement sleep across days. Thus, neonatal fentanyl exposure leads to altered sleep-wake states during adolescence in mice.
Keywords: Circadian; Fentanyl; Neonatal; Opioids; Sleep.
Copyright © 2025 International Brain Research Organization (IBRO). Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Update of
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Sleep and circadian rhythm activity alterations during adolescence in a mouse model of neonatal fentanyl withdrawal syndrome.bioRxiv [Preprint]. 2024 Jul 9:2024.07.05.602239. doi: 10.1101/2024.07.05.602239. bioRxiv. 2024. Update in: Neuroscience. 2025 Mar 17;569:85-91. doi: 10.1016/j.neuroscience.2025.01.064. PMID: 39026736 Free PMC article. Updated. Preprint.
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