Evidence map›Paper›PMID 40597281›Full record

ArticleJournal of cannabis research2025

Orally consumed cannabinoids: the effect of carrier oil on acute tissue distribution in male C57BL/6 mice.

Cody A C Lust, Lyn M Hillyer, Mitchell Pallister, Amanda J Wright, Michael A Rogers, Erin M Rock, Cheryl L Limebeer, Linda A Parker, David W L Ma

Abstract read
In one paragraph

Article in Journal of cannabis research, 2025. 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. Article
  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.

Cody A C LustDepartment of Human Health and Nutritional Sciences, University of Guelph, Guelph, ON, N1G2W1, Canada.
Lyn M HillyerDepartment of Human Health and Nutritional Sciences, University of Guelph, Guelph, ON, N1G2W1, Canada.
Mitchell PallisterDepartment of Human Health and Nutritional Sciences, University of Guelph, Guelph, ON, N1G2W1, Canada.
Amanda J WrightDepartment of Human Health and Nutritional Sciences, University of Guelph, Guelph, ON, N1G2W1, Canada.
Michael A RogersDepartment of Food Science, Guelph, Canada.
Erin M RockDepartment of Psychology and Collaborative Neuroscience Program, ON, Guelph, N1G2W1, Canada.
Cheryl L LimebeerDepartment of Psychology and Collaborative Neuroscience Program, ON, Guelph, N1G2W1, Canada.
Linda A ParkerDepartment of Psychology and Collaborative Neuroscience Program, ON, Guelph, N1G2W1, Canada.
David W L MaDepartment of Human Health and Nutritional Sciences, University of Guelph, Guelph, ON, N1G2W1, Canada. davidma@uoguelph.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFundamental gaps in knowledge exist in understanding the tissue distribution of cannabinoids, cannabidiol (CBD) and tetrahydrocannabinol (THC), following oral ingestion. CBD and THC are lipid-soluble and oral bioavailability is increased when combined with long-chain fatty acid carrier oils prior to oral ingestion. Oils with eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) confer positive health benefits and have yet to be examined as a carrier oil for oral cannabinoid delivery thus, examination is warranted.

methodsThis study investigated the acute tissue distribution of cannabinoids in serum, adipose, brain, liver, heart, and muscle of male C57BL/6 mice at 1, 2, and 3 h (H) post oral ingestion. Mice were gavaged with CBD (5 mg/kg) and THC (1 mg/kg) combined with either sesame (SES), mixed EPA/DHA, or DHA enriched (DHA) oil as a carrier. With assistance of the Analytical Facility for Bioactive Molecules (Toronto, Canada), tissue concentration of cannabinoids was quantified using liquid chromatography with tandem mass spectrometry.

resultsSES oil resulted in a significantly greater concentration of CBD and THC (p < 0.05) across all tissues and times compared to the n-3 polyunsaturated fatty acid (PUFA) oils. The ratio of EPA:DHA in the carrier oils modestly affected distribution of cannabinoids to tissues, notably, DHA oil resulted in a greater concentration of CBD in the brain. Heart tissue had the highest concentration of CBD at 1 and 2H post-oral gavage, and adipose tissue had the highest concentration at 3H which was consistent across all three carrier oils.

conclusionsThis study profiled the greatest number of tissues to-date for the acute distribution of CBD and THC following oral consumption with a lipid carrier in mice which demonstrated a non-uniform distribution to tissues over time. SES oil proved to be far more effective as a carrier oil at delivering orally consumed cannabinoids to tissues compared to two different n-3 PUFA containing oils. Further developing our fundamental understanding of cannabinoid distribution across tissues following their consumption from foods and pharmaceuticals are necessary to establish specific pharmacokinetic profiles to aid oral dosing strategies and maximize the bioactive potential of cannabinoids.

Indexed as

CannabinoidsCBDMiceOmega-3OralSesameTHCTissue distribution

Identifiers

PMID40597281
PMCPMC12219598

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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.