Evidence map›Paper›PMID 38270614›Full record

ArticlePsychopharmacology2024

Activation of NOP receptor increases vulnerability to stress: role of glucocorticoids and CRF signaling.

Victor A D Holanda, Raissa N de Almeida, Matheus C de Oliveira, Edilson D da Silva Junior, Nicole L Galvão-Coelho, Girolamo Calo', Chiara Ruzza, Elaine C Gavioli

Abstract read
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In one paragraph

Article in Psychopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

8 authors at 3 institutions in 2 countries.

Victor A D HolandaDepartment of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Av. Senador salgado Filho, 3000, Campus Universitário - Lagoa Nova, Natal, 59078-900, Brazil.
Raissa N de AlmeidaDepartment of Physiology and Behavior and Postgraduate Program in Psychobiology, Federal University of Rio Grande do Norte, Natal, Brazil.
Matheus C de OliveiraDepartment of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Av. Senador salgado Filho, 3000, Campus Universitário - Lagoa Nova, Natal, 59078-900, Brazil.
Edilson D da Silva JuniorDepartment of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Av. Senador salgado Filho, 3000, Campus Universitário - Lagoa Nova, Natal, 59078-900, Brazil.
Nicole L Galvão-CoelhoDepartment of Physiology and Behavior and Postgraduate Program in Psychobiology, Federal University of Rio Grande do Norte, Natal, Brazil.
Girolamo Calo'Department of Pharmaceutical and Pharmacological Sciences, University of Padua, Padua, Italy.
Chiara RuzzaDepartment of Neuroscience and Rehabilitation, University of Ferrara, Ferrara, Italy.
Elaine C GavioliDepartment of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Av. Senador salgado Filho, 3000, Campus Universitário - Lagoa Nova, Natal, 59078-900, Brazil. egavioli@hotmail.com.ORCID http://orcid.org/0000-0001-8967-1369
Universidade Federal do Rio Grande do Norte · BRUniversity of Ferrara · ITUniversity of Padua · IT

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 303072/2019-9Conselho Nacional de Desenvolvimento Científico e Tecnológico 401837/2016-5Coordenação de Aperfeiçoamento de Pessoal de Nível Superior PNPD fellowship
6 · The paper itself

Abstract

rationaleRecently, we demonstrated that the activation of the nociceptin/orphanin FQ (N/OFQ) receptor (NOP) signaling facilitates depressive-like behaviors. Additionally, literature findings support the ability of the N/OFQ-NOP system to modulate the hypothalamic-pituitary-adrenal (HPA) axis.

objectivesConsidering that dysfunctional HPA axis is strictly related to stress-induced psychopathologies, we aimed to study the role of the HPA axis in the pro-depressant effects of NOP agonists.

methodsMice were treated prior to stress with the NOP agonist Ro 65-6570, and immobility time in the forced swimming task and corticosterone levels were measured. Additionally, the role of endogenous glucocorticoids and CRF was investigated using the glucocorticoid receptor antagonist mifepristone and the CRF

resultsThe NOP agonist in a dose-dependent manner further increased the immobility of mice in the second swimming session compared to vehicle. By contrast, under the same conditions, the administration of the NOP antagonist SB-612111 before stress reduced immobility, while the antidepressant nortriptyline was inactive. Concerning in-serum corticosterone in mice treated with vehicle, nortriptyline, or SB-612111, a significant decrease was observed after re-exposition to stress, but no differences were detected in Ro 65-6570-treated mice. Administration of mifepristone or antalarmin blocked the Ro 65-6570-induced increase in the immobility time in the second swimming session.

conclusionsPresent findings suggest that NOP agonists increase vulnerability to depression by hyperactivating the HPA axis and then increasing stress circulating hormones and CRF

Indexed as

CycloheptanesImidazolesOpioid PeptidesPiperidinesReceptors, OpioidSpiro CompoundsAnimalsCorticosteroneGlucocorticoidsHypothalamo-Hypophyseal SystemMiceMifepristoneNociceptin ReceptorNortriptylinePituitary-Adrenal System8-acenaphthen-1-yl-1-phenyl-1,3,8-triazaspiro(4.5)decan-4-onecis-1-methyl-7-((4-(2,6-dichlorophenyl)piperidin-1-yl)methyl)-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-olCorticosteroneCycloheptanesGlucocorticoidsImidazolesMifepristoneNociceptin ReceptorNortriptylineOpioid PeptidesPiperidinesReceptors, OpioidSpiro CompoundsDepressionForced swimmingHypothalamic-pituitary-adrenal axismouseNociceptin/orphanin FQStress susceptibility

Identifiers

PMID38270614
OpenAlexW4391228903

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.