Evidence map›Paper›PMID 39083456›Full record

ArticlePloS one2024

Effects of in utero delta-9-tetrahydrocannabinol (THC) exposure on fetal and infant musculoskeletal development in a preclinical nonhuman primate model.

Samantha A Moellmer, Olivia L Hagen, Parsa A Farhang, Victoria R Duke, Meghan E Fallon, Monica T Hinds, Owen J T McCarty, Jamie O Lo, Karina H Nakayama

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Prenatal Cannabis and Tobacco: Studies in Animal Models.Advances in experimental medicine and biology · 2026
    Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Samantha A MoellmerDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, United States of America.
Olivia L HagenDivision of Reproduction and Developmental Sciences, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR, United States of America.ORCID 0009-0001-0369-5819
Parsa A FarhangDepartment of Molecular Microbiology and Immunology, Johns Hopkins University, Baltimore, MD, United States of America.
Victoria R DukeDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, United States of America.
Meghan E FallonYale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine, New Haven, CT, United States of America.ORCID 0000-0002-5868-7576
Monica T HindsDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, United States of America.
Owen J T McCartyDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, United States of America.
Jamie O LoDivision of Reproduction and Developmental Sciences, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR, United States of America.ORCID 0000-0002-1934-1935
Karina H NakayamaDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR, United States of America.ORCID 0000-0001-5426-7446

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
Characterization of Coagulation Factor-platelet Interactions: Role of FXIR01HL101972 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Owen J McCarty · 2010 to 2026
$8.5M
Effects of human milk handling practices on peptide release and bioactivity in the preterm infant intestineR01HD097367 · NICHD · OREGON STATE UNIVERSITY · PI David Charles Dallas · 2022 to 2026
$3.0M
Impact of maternal marijuana use on epigenetic regulation of offspring neurodevelopmentDP1DA056493 · NIDA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Jamie Lo · 2022 to 2026
$2.6M
PORT (Portland Oral health Research Training)T90DE030859 · NIDCR · OREGON HEALTH & SCIENCE UNIVERSITY · PI WU, HUI · 2021 to 2025
$2.1M
Regenerative engineering for complex extremity traumaR01AR080150 · NIAMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Karina Nakayama · 2023 to 2026
$2.1M
NHLBI NIH HHS R01 HL101972NIAMS NIH HHS R01 AR080150NICHD NIH HHS R01 HD097367NIDA NIH HHS DP1 DA056493NIDCR NIH HHS T90 DE030859NIH HHS P51 OD011092
6 · The paper itself

Abstract

The endocannabinoid system (ECS) plays a major role in the maintenance of bodily homeostasis and adaptive response to external insults. It has been shown to regulate crucial physiological processes and behaviors, spanning nervous functions, anxiety, cognition, and pain sensation. Due to this broad activity, the ECS has been explored as a potential therapeutic target in the treatment of select diseases. However, until there is a more comprehensive understanding of how ECS activation by exogenous and endogenous ligands manifests across disparate tissues and cells, discretion should be exercised. Previous work has investigated how endogenous cannabinoid signaling impacts skeletal muscle development and differentiation. However, the effects of activation of the ECS by delta-9-tetrahydrocannabinol (THC, the most psychoactive component of cannabis) on skeletal muscle development, particularly in utero, remain unclear. To address this research gap, we used a highly translational non-human primate model to examine the potential impact of chronic prenatal THC exposure on fetal and infant musculoskeletal development. RNA was isolated from the skeletal muscle and analyzed for differential gene expression using a Nanostring nCounter neuroinflammatory panel comprised of 770 genes. Histomorphological evaluation of muscle morphology and composition was also performed. Our findings suggest that while prenatal THC exposure had narrow overall effects on fetal and infant muscle development, the greatest impacts were observed within pathways related to inflammation and cytokine signaling, which suggest the potential for tissue damage and atrophy. This pilot study establishes feasibility to evaluate neuroinflammation due to prenatal THC exposure and provides rationale for follow-on studies that explore the longer-term implications and functional consequences encountered by offspring as they continue to mature.

Indexed as

DronabinolMuscle, SkeletalPrenatal Exposure Delayed EffectsAnimalsFemaleFetal DevelopmentMacaca mulattaMaleMusculoskeletal DevelopmentPregnancyDronabinol

Identifiers

PMID39083456
PMCPMC11290632

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.