Evidence map›Paper›PMID 34512286›Full record

ArticleFrontiers in behavioral neuroscience2021

Cannabidiol Exposure During the Mouse Adolescent Period Is Without Harmful Behavioral Effects on Locomotor Activity, Anxiety, and Spatial Memory.

J S Kaplan, J K Wagner, K Reid, F McGuinness, S Arvila, M Brooks, H Stevenson, J Jones, B Risch, T McGillis and 3 more

Abstract read
In one paragraph

Article in Frontiers in behavioral neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–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

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  7. Long-Term Treatment with Cannabidiol-EnrichedInternational journal of molecular sciences · 2023
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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

13 authors.

J S KaplanDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
J K WagnerDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
K ReidDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
F McGuinnessDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
S ArvilaDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
M BrooksDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
H StevensonDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
J JonesDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
B RischDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
T McGillisDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
R BudinichDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
E GambellDepartment of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
B PredovichPrelabs, Lehigh Acres, FL, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cannabidiol (CBD) is a non-intoxicating phytocannabinoid whose purported therapeutic benefits and impression of a high safety profile has promoted its increasing popularity. CBD's popularity is also increasing among children and adolescents who are being administered CBD, off label, for the treatment of numerous symptoms associated with autism spectrum disorder, attention deficit hyperactivity disorder, anxiety, and depression. The relative recency of its use in the adolescent population has precluded investigation of its impact on the developing brain and the potential consequences that may present in adulthood. Therefore, there's an urgency to identify whether prolonged adolescent CBD exposure has substantive impacts on the developing brain that impact behavioral and cognitive processes in adulthood. Here, we tested the effect of twice-daily intraperitoneal administrations of CBD (20 mg/kg) in male and female C57BL/6J mice during the adolescent period of 25-45 days on weight gain, and assays for locomotor behavior, anxiety, and spatial memory. Prolonged adolescent CBD exposure had no detrimental effects on locomotor activity in the open field, anxiety behavior on the elevated plus maze, or spatial memory in the Barnes Maze compared to vehicle-treated mice. Interestingly, CBD-treated mice had a faster rate of learning in the Barnes Maze. However, CBD-treated females had reduced weight gain during the exposure period. We conclude that prolonged adolescent CBD exposure in mice does not have substantive negative impacts on a range of behaviors in adulthood, may improve the rate of learning under certain conditions, and impacts weight gain in a sex-specific manner.

Indexed as

adolescenceanxietycannabidiolcannabinoidcannabisdevelopmentlearningweight

Identifiers

PMID34512286
PMCPMC8426900

What OpenQuestion holds

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LicenceCC BY
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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.