Evidence map›Paper›PMID 39229006›Full record

ArticlebioRxiv : the preprint server for biology2025

Anxiety and risk-taking behavior maps onto opioid and alcohol polysubstance consumption patterns in male and female mice.

Makenzie Patarino, Ziheng Christina Wang, Andrew Byungwook Kim, Katrina Wong, Suhjung Janet Lee, Emma Skillen, Richa Nag, Britahny Baskin, Abigail G Schindler

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

9 authors.

Makenzie PatarinoDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA 98195.
Ziheng Christina WangVA Northwest Geriatric Research Education and Clinical Center, VA Puget Sound Health Care System, Seattle, WA 98108, USA.
Andrew Byungwook KimWestern Governors University, Millcreek, UT 84107, USA.
Katrina WongDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA 98195.
Suhjung Janet LeeVA Northwest Geriatric Research Education and Clinical Center, VA Puget Sound Health Care System, Seattle, WA 98108, USA.
Emma SkillenDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA 98195.
Richa NagDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA 98195.
Britahny BaskinDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA 98195.
Abigail G SchindlerDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA 98195.ORCID 0000-0002-7039-1348

Funding

University of Washington Center of Excellence in Opioid Addiction ResearchP30DA048736 · NIDA · UNIVERSITY OF WASHINGTON · PI Charles Chavkin · 2019 to 2026
$13.0M
Psychology Training in Alcohol Research (PTAR)T32AA007455 · NIAAA · UNIVERSITY OF WASHINGTON · PI MARY E. LARIMER · 1985 to 2026
$11.4M
TRAINING IN THE MOLECULAR PHARMACOLOGY OF ABUSED DRUGST32DA007278 · NIDA · UNIVERSITY OF WASHINGTON · PI Susan Marie Ferguson, Paul E. M. Phillips · 1993 to 2026
$9.8M
Neural Mechanisms of Impulsivity and Attention Following Traumatic Brain InjuryIK2BX003258 · VA · VA PUGET SOUND HEALTHCARE SYSTEM · PI SCHINDLER, ABIGAIL G · 2017 to 2021
–
BLRD VA I01 BX005582BLRD VA IK2 BX003258NIAAA NIH HHS T32 AA007455NIDA NIH HHS P30 DA048736NIDA NIH HHS T32 DA007278
6 · The paper itself

Abstract

Polysubstance use is prevalent in the population but remains understudied in preclinical models. Alcohol and opioid polysubstance use is associated with negative outcomes, worse treatment prognosis, and higher overdose risk; but underlying mechanisms are still being uncovered. Examining factors that motivate use of one substance over another in different contexts in preclinical models will better our understanding of polysubstance use and improve translational value. Here we assessed baseline anxiety-like and locomotive behavior and then measured voluntary consumption of multiple doses of alcohol and fentanyl in group housed male and female mice using our novel Socially Integrated Polysubstance (SIP) system. Fifty-six male (n=32) and female (n=24) adult mice were housed in groups of 4 for one week with continuous access to food, water, two doses of ethanol (5% and 10%) and two doses of fentanyl (5 ug/ml and 20 ug/ml). Our analyses revealed sex differences across multiple domains - female mice consumed more liquid in the dark cycle, had higher activity, a higher preference for both ethanol and fentanyl over water, and their fentanyl preference increased over the seven days. Furthermore, both male and female mice displayed polysubstance consumption patterns, with female mice displaying more prolonged polysubstance use across days in the SIP chambers. We then used machine-learning techniques to reveal underlying relationships between baseline behavioral phenotypes and subsequent polysubstance consumption patterns, where anxiety- and risk-taking-like behavioral phenotypes mapped onto discrete patterns of polysubstance use, preference, and escalation. By simulating more translationally relevant substance use and improving our understanding of the motivations for different patterns of consumption, this study contributes to the developing preclinical literature on polysubstance use with the goal of facilitating better treatment outcomes and novel therapeutic strategies.

Indexed as

AlcoholAnxietyEthanolFentanylIndividual differencesLocomotionNoveltyOpioidsPolysubstanceSex differencesSubstance Use Disorder

Identifiers

PMID39229006
PMCPMC11370560

What OpenQuestion holds

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Registered trials

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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.