Evidence map›Paper›PMID 39975197›Full record

ArticlebioRxiv : the preprint server for biology2025

Early Life Outcomes of Prenatal Exposure to Alcohol and Synthetic Cannabinoids in Mice.

Siara K Rouzer, McKay Domen, Aisley George, Abigail Bowring, Rajesh C Miranda

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

5 authors.

Siara K RouzerDepartment of Neuroscience and Experimental Therapeutics, Texas A&M College of Medicine, 8447 John Sharp Parkway, Bryan, TX 77807, United States.ORCID 0000-0002-5860-9308
McKay DomenDepartment of Neuroscience and Experimental Therapeutics, Texas A&M College of Medicine, 8447 John Sharp Parkway, Bryan, TX 77807, United States.
Aisley GeorgeDepartment of Neuroscience and Experimental Therapeutics, Texas A&M College of Medicine, 8447 John Sharp Parkway, Bryan, TX 77807, United States.
Abigail BowringDepartment of Neuroscience and Experimental Therapeutics, Texas A&M College of Medicine, 8447 John Sharp Parkway, Bryan, TX 77807, United States.ORCID 0009-0005-0028-9443
Rajesh C MirandaDepartment of Neuroscience and Experimental Therapeutics, Texas A&M College of Medicine, 8447 John Sharp Parkway, Bryan, TX 77807, United States.ORCID 0000-0002-8359-892X

Funding

Prenatal alcohol/cannabinoid co-exposures and fetal brain developmentR01AA028406 · NIAAA · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI LARIN, KIRILL V, MIRANDA, RAJESH C · 2020 to 2024
$2.6M
Simultaneous prenatal alcohol and cannabinoid exposure & offspring corticostriatal neurocircuitryF32AA029866 · NIAAA · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ROUZER, SIARA · 2022 to 2024
$200k
NIAAA NIH HHS F32 AA029866NIAAA NIH HHS L40 AA030427NIAAA NIH HHS R01 AA028406
6 · The paper itself

Abstract

This study explores the effects of prenatal co-exposure to alcohol and synthetic cannabinoids on offspring viability, physical development, and neurobehavioral outcomes in young adulthood. The aim is to identify distinct outcomes of co-exposure compared to single-drug exposures and to examine potential sex-specific vulnerabilities in motor coordination and exploratory behaviors. Pregnant C57Bl/6J mice were assigned to one of four treatment groups: Control, Alcohol-exposed, Cannabinoid-exposed, or Alcohol+Cannabinoid-exposed, with drug administration occurring between Gestational Days 12-15. Offspring were first evaluated at birth for survival, physical malformations, and developmental delays. Subsequently, young adult offspring were assessed for motor coordination using rotarod tests and exploratory behavior using open field tests. Our results indicate that alcohol and cannabinoid co-exposure significantly reduced offspring survival and litter sizes compared to controls. Non-viable offspring displayed craniofacial abnormalities, limb malformations, and developmental delays. Behavioral assessments in young adulthood demonstrated that all forms of prenatal drug exposure impaired motor coordination in males, while alcohol and cannabinoid exposures independently produced impairments in females. In the open field test, co-exposed male offspring exhibited reduced center exploration, indicative of anxiety-like behavior. Co-exposed offspring, regardless of sex, demonstrated hyperactivity, characterized by increased speed and distance traveled. Together, these findings underscore the heightened risks associated with prenatal polysubstance exposure, which exacerbates offspring mortality and induces sex-specific neurobehavioral deficits. This study highlights the distinct outcomes associated with prenatal co-exposure, and the need for future research to investigate underlying mechanisms driving these developmental disruptions and sex-specific susceptibilities.

Indexed as

AlcoholCannabinoidMotor behaviorPrenatalSex differencesSurvival

Identifiers

PMID39975197
PMCPMC11838379

What OpenQuestion holds

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LicenceCC BY-NC
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.