Evidence map›Paper›PMID 31250073›Full record

ArticlePsychopharmacology2019

CB1 receptor antagonism in capuchin monkeys alters social interaction and aversive memory extinction.

Natália Gonczarowska, Carlos Tomaz, Fabio V Caixeta, Renato Malcher-Lopes, Marilia Barros, Hisao Nishijo, Rafael S Maior

Abstract read
PubMed Publisher
In one paragraph

Article in Psychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Combinatorial approaches for treating neuropsychiatric social impairment.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  3. 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

7 authors at 2 institutions in 4 countries.

Natália GonczarowskaPrimate Center, Institute of Biology, University of Brasília, Brasilia, DF, Brazil.
Carlos TomazPrimate Center, Institute of Biology, University of Brasília, Brasilia, DF, Brazil.
Fabio V CaixetaLaboratory of Neuroscience and Behavior, Department of Physiological Sciences, Institute of Biological Sciences, University of Brasília, Brasilia, DF, 70910-900, Brazil.
Renato Malcher-LopesLaboratory of Neuroscience and Behavior, Department of Physiological Sciences, Institute of Biological Sciences, University of Brasília, Brasilia, DF, 70910-900, Brazil.
Marilia BarrosPrimate Center, Institute of Biology, University of Brasília, Brasilia, DF, Brazil.
Hisao NishijoSystem Emotional Science, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Sugitani, Toyama, 2630, Japan.
Rafael S MaiorPrimate Center, Institute of Biology, University of Brasília, Brasilia, DF, Brazil. rsmaior@unb.br.ORCID http://orcid.org/0000-0001-7219-8675
Universidade de Brasília · BRUniversity of Toyama · JP

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 304041/2015-7Conselho Nacional de Desenvolvimento Científico e Tecnológico 310719/2017-8Conselho Nacional de Desenvolvimento Científico e Tecnológico 455532/2014-1Coordination for the improvement of higher education personnel (CAPES) N/A
6 · The paper itself

Abstract

rationaleThe endocannabinoid system (eCS) is an important modulator of social anxiety and social reward, as well as memory functions.

objectivesThe present study evaluated the role of eCS in social interactions and aversive memory extinction in capuchin monkeys (Sapajus spp.) by blocking the cannabinoid type 1 receptor (CB

methodsIn experiment 1, spontaneous social and non-social behaviors of five capuchin males, each one living in triads with two other females, were observed after AM251 treatment (vehicle, 0.3, 1.0, and 3.0 mg/kg; i.m.). In experiment 2, seven male capuchin monkeys were trained to reach for a reward inside a wooden box. After training, they were given either vehicle or a 3.0-mg/kg i.m. dose of AM251 before a single aversive encounter with a live snake in the box. The latency to return to reach the reward inside the box in subsequent trials was measured.

resultsThe 3.0-mg/kg dose significantly increased the time spent performing self-directed behaviors, while decreasing that of social interactions. No changes were observed in vigilance or locomotion. AM251 increased the latency to reach the reward after the aversive encounter.

conclusionTaken together, these results suggest that CB

Indexed as

Interpersonal RelationsAnimalsAvoidance LearningCebusDose-Response Relationship, DrugFearFemaleMaleMemoryPiperidinesPyrazolesRandom AllocationReceptor, Cannabinoid, CB1RewardAM 251PiperidinesPyrazolesReceptor, Cannabinoid, CB1AM-251Aversive memoryCapuchin monkeyEndocannabinoid systemSocial interaction

Identifiers

PMID31250073
OpenAlexW2955591399

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.