Evidence map›Paper›PMID 37397463›Full record

ArticleFrontiers in neuroscience2023

Cannabidiol and cannabis-inspired terpene blends have acute prosocial effects in the BTBR mouse model of autism spectrum disorder.

Jenika Staben, Megan Koch, Keelee Reid, Jessica Muckerheide, Lauren Gilman, Finn McGuinness, Sarina Kiesser, Iain W H Oswald, Kevin A Koby, Thomas J Martin and 1 more

Abstract read
In one paragraph

Article in Frontiers in neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Cannabis and cannabinoid research · 2024
    Article
  4. Article
  5. Article
  6. Review
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

11 authors.

Jenika StabenDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
Megan KochDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
Keelee ReidDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
Jessica MuckerheideDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
Lauren GilmanDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
Finn McGuinnessDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
Sarina KiesserScientific Technical Services, Western Washington University, Bellingham, WA, United States.
Iain W H OswaldDepartment of Research and Development, Abstrax Tech, Inc., Tustin, CA, United States.
Kevin A KobyDepartment of Research and Development, Abstrax Tech, Inc., Tustin, CA, United States.
Thomas J MartinDepartment of Research and Development, Abstrax Tech, Inc., Tustin, CA, United States.
Joshua S KaplanDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Cannabidiol (CBD) is a non-intoxicating phytocannabinoid with increasing popularity due to its purported therapeutic efficacy for numerous off-label conditions including anxiety and autism spectrum disorder (ASD). Those with ASD are commonly deficient in endogenous cannabinoid signaling and GABAergic tone. CBD has a complex pharmacodynamic profile that includes enhancing GABA and endocannabinoid signaling. Thus, there is mechanistic justification for investigating CBD's potential to improve social interaction and related symptoms in ASD. Recent clinical trials in children with ASD support CBD's beneficial effects in numerous comorbid symptoms, but its impact on social behavior is understudied. Methods: Here, we tested the prosocial and general anxiolytic efficacy of a commercially available CBD-rich broad spectrum hemp oil delivered by repeated puff vaporization and consumed via passive inhalation in the female cohort of the BTBR strain, a common inbred mouse line for preclinical assessment of ASD-like behaviors. Results: We observed that CBD enhanced prosocial behaviors using the 3-Chamber Test with a different vapor dose-response relationship between prosocial behavior and anxiety-related behavior on the elevated plus maze. We also identified that inhalation of a vaporized terpene blend from the popular OG Kush cannabis strain increased prosocial behavior independently of CBD and acted together with CBD to promote a robust prosocial effect. We observed similar prosocial effects with two additional cannabis terpene blends from the Do-Si-Dos and Blue Dream strains, and further reveal that these prosocial benefits rely on the combination of multiple terpenes that comprise the blends. Discussion: Our results illustrate the added benefit of cannabis terpene blends for CBD-based treatment of ASD.

Indexed as

autism spectrum disordercannabidiolcannabinoidcannabisCBDsocial behaviorterpenesvolatile organic compounds

Identifiers

PMID37397463
PMCPMC10311644

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.