Evidence map›Paper›PMID 34207178›Full record

ArticleMolecules (Basel, Switzerland)2021

Increasing Endocannabinoid Tone Alters Anxiety-Like and Stress Coping Behaviour in Female Rats Prenatally Exposed to Valproic Acid.

Aoife M Thornton, Rachel M Humphrey, Daniel M Kerr, David P Finn, Michelle Roche

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
2.4field-weighted citation impact, top 11% of its field
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, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. 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

5 authors at 1 institution in 1 country.

Aoife M ThorntonPhysiology, School of Medicine, National University of Ireland Galway, H91 W5P7 Galway, Ireland.
Rachel M HumphreyPhysiology, School of Medicine, National University of Ireland Galway, H91 W5P7 Galway, Ireland.ORCID 0000-0002-5157-5010
Daniel M KerrPharmacology and Therapeutics, School of Medicine, National University of Ireland Galway, H91 W5P7 Galway, Ireland.
David P FinnGalway Neuroscience Centre, National University of Ireland Galway, H91 W5P7 Galway, Ireland.ORCID 0000-0001-6186-621X
Michelle RochePhysiology, School of Medicine, National University of Ireland Galway, H91 W5P7 Galway, Ireland.ORCID 0000-0002-7242-9397
Ollscoil na Gaillimhe – University of Galway · IE

Funding

National University of Ireland, Galway 00000
6 · The paper itself

Abstract

Given the sex differences evident in the prevalence of autism, there is an increased awareness of the importance of including females in autism research to determine sexual dimorphism and sex-specific treatments. Cannabinoids and endocannabinoid modulators have been proposed as potential novel treatments for autism-related symptoms; however, few studies to date have examined if these pharmacological agents elicit sex-specific effects. The aim of the present study was to use the valproic acid (VPA) model of autism to compare the behavioural responses of male and female rats and examine the effects of increasing endocannabinoid tone on the behavioural responses of VPA-exposed female rats. These data revealed that VPA-exposed male, but not female, rats exhibit reduced social responding in the three-chamber and olfactory habituation/dishabituation (OHD) test during adolescence. In comparison, VPA-exposed female, but not male, adolescent rats exhibited anxiety-like behaviour in the elevated plus maze (EPM) and open field test (OFT). In VPA-exposed female rats, increasing 2-AG levels augmented anxiety-like behaviour in the EPM and OFT, while increasing AEA levels reduced stress coping behaviour in the swim stress test. These data highlight sexual dimorphic behaviours in the VPA model and indicate that enhancing endocannabinoid levels may exacerbate negative affective behaviour in VPA-exposed females. Thus, considerations should be paid to the possible sex-specific effects of cannabinoids for the treatment of symptoms associated with autism.

Indexed as

AnimalsAnxietyAnxiety DisordersAutistic DisorderBehavior, AnimalDisease Models, AnimalEndocannabinoidsFemaleMalePregnancyPrenatal Exposure Delayed EffectsPsychological DistressRatsRats, Sprague-DawleyValproic AcidEndocannabinoidsValproic Acid2-AGanandamideautismFAAHMGLsex differencessocial behaviourVPA

Identifiers

PMID34207178
PMCPMC8233839
OpenAlexW3174068514

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.