Evidence map›Paper›PMID 41000765›Full record

ArticlebioRxiv : the preprint server for biology2025

Effects of acute adolescent stress on the acquisition and maintenance of intravenous oxycodone self-administration in male and female rats.

Corinne A Gallagher, Daniel J Chandler, Daniel F Manvich

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Corinne A GallagherDepartment of Neuroscience, Rowan-Virtua School of Osteopathic Medicine, 42 East Laurel Rd, Suite 2200, Stratford, NJ 08084.
Daniel J ChandlerDepartment of Neuroscience, Rowan-Virtua School of Osteopathic Medicine, 42 East Laurel Rd, Suite 2200, Stratford, NJ 08084.
Daniel F ManvichDepartment of Neuroscience, Rowan-Virtua School of Osteopathic Medicine, 42 East Laurel Rd, Suite 2200, Stratford, NJ 08084.

Funding

Stress-induced locus coeruleus dysfunction as a mediator of opioid abuseR21DA052815 · NIDA · ROWAN UNIVERSITY SCHOOL/OSTEOPATHIC MED · PI CHANDLER, DANIEL · 2021 to 2022
$449k
Counteracting cardiorespiratory and subjective effects of fentanyl-xylazine mixtures using a dual antagonist approachR21DA062164 · NIDA · ROWAN UNIVERSITY SCHOOL/OSTEOPATHIC MED · PI MANVICH, DANIEL F., MARTINEZ, DIANA · 2024 to 2024
$424k
NIDA NIH HHS R21 DA052815NIDA NIH HHS R21 DA062164
6 · The paper itself

Abstract

Background: The persistent threat of the opioid epidemic warrants investigation into risk factors that predispose individuals to opioid use disorder (OUD). Adolescent stress has been linked to enhanced risk for OUD in humans, however attempts to model this preclinically have yielded mixed results. Additionally, few studies have explored whether adolescent stress modulates the reinforcing effects of prescription opioids. Here we investigate the impact of acute adolescent stress on oxycodone self-administration in male and female rats. Methods: Adolescent male and female rats underwent acute restraint stress during concurrent exposure to predator odor, or control handling. Approximately one week later, subjects were allowed to acquire IV oxycodone self-administration (0.03 mg/kg/inf) over 10 sessions (2 h/day) under a fixed-ratio 1 (FR1) schedule of reinforcement. Following three additional FR1 sessions and seven sessions under FR3, rats underwent two progressive-ratio tests (0.03 mg/kg/inf and 0.06 mg/kg/inf, respectively). Separate groups of adolescent rats underwent similar experimental manipulations but were trained on sucrose reinforcement. Results: Adolescent stress did not affect the rate of acquisition of IV oxycodone self-administration. However, oxycodone self-administration escalated during post-acquisition FR1 sessions and remained elevated during FR3 sessions in stressed rats as compared to unstressed controls. Adolescent stress exposure did not affect responding during progressive-ratio tests, nor did it affect any measure of sucrose pellet reinforcement. Conclusions: The present results are the first to demonstrate adolescent stress-induced enhancement of oxycodone reinforcement in rats and provide a preclinical model for investigating the neurobiological mechanisms by which adolescent stress increases vulnerability for prescription opioid misuse.

Indexed as

adolescent stressoxycodonePrescription opioidsself-administration

Identifiers

PMID41000765
PMCPMC12458122

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.