Evidence map›Paper›PMID 25707915›Full record

ArticleMolecular neurobiology2016

The Pronociceptive Effect of Paradoxical Sleep Deprivation in Rats: Evidence for a Role of Descending Pain Modulation Mechanisms.

Dabna H Tomim, Felipe M Pontarolla, Jessica F Bertolini, Mauricio Arase, Glaucia Tobaldini, Marcelo M S Lima, Luana Fischer

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

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  10. At the Intersection of Pain and Sleep: a Roadmap for Preclinical Pain Research.Frontiers in pain research (Lausanne, Switzerland) · 2025
    Review
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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

7 authors at 1 institution in 1 country.

Dabna H TomimDepartment of Physiology, Division of Biological Sciences, Federal University of Parana, Curitiba, Parana, Brazil.
Felipe M PontarollaDepartment of Physiology, Division of Biological Sciences, Federal University of Parana, Curitiba, Parana, Brazil.
Jessica F BertoliniDepartment of Physiology, Division of Biological Sciences, Federal University of Parana, Curitiba, Parana, Brazil.
Mauricio AraseDepartment of Physiology, Division of Biological Sciences, Federal University of Parana, Curitiba, Parana, Brazil.
Glaucia TobaldiniDepartment of Physiology, Division of Biological Sciences, Federal University of Parana, Curitiba, Parana, Brazil.
Marcelo M S LimaDepartment of Physiology, Division of Biological Sciences, Federal University of Parana, Curitiba, Parana, Brazil.
Luana FischerDepartment of Physiology, Division of Biological Sciences, Federal University of Parana, Curitiba, Parana, Brazil. fischer@ufpr.br.
Universidade Federal do Paraná · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanisms underlying the pronociceptive effect of paradoxical sleep deprivation (PSD) are not known. In this study, we asked whether PSD increases tonic nociception in the formalin test, decreases the antinociceptive effect of morphine administered into the periaqueductal gray matter (PAG), and disrupts endogenous descending pain modulation. PSD for either 24 or 48 h significantly increased formalin-induced nociception and decreased mechanical nociceptive paw withdrawal threshold. The maximal antinociceptive effect induced by morphine (0.9-9 nmol, intra-PAG) was significantly decreased by PSD. The administration of a low dose of the GABAA receptor antagonist, bicuculline (30-300 pmol, intra-PAG), decreased nociception in control rats, but not in paradoxical-sleep-deprived ones. Furthermore, the administration of the cholecystokinin (CCK) 2 receptor antagonist, YM022 (0.5-2 pmol) in the rostral ventral medulla (RVM), decreased nociception in paradoxical-sleep-deprived rats but not in control ones. While a dose of the CCK 2 receptor agonist, CCK-8 (8-24 pmol intra-RVM), increased nociception in control rats, but not in paradoxical-sleep-deprived ones. In addition, the injection of lidocaine (QX-314, 2%, intra-RVM) decreased nociception in sleep-deprived rats, but not in control rats, while the lesion of the dorsolateral funiculus prevented the pronociceptive effect of PSD. Finally, PSD significantly increased c-Fos expression in the RVM. Therefore, PSD increases pain independently of its duration or of the characteristic of the nociceptive stimulus and decreases morphine analgesia at the PAG. PSD appears to increase pain by decreasing descending pain inhibitory activity and by increasing descending pain facilitatory activity.

Indexed as

NociceptionAnimalsBicucullineLidocaineMaleMorphineMotor ActivityPainPain MeasurementPeriaqueductal GrayProto-Oncogene Proteins c-fosRats, WistarSleep DeprivationBicucullineLidocaineMorphineProto-Oncogene Proteins c-fosQX-314Descending pain modulationMorphineNociceptionPainParadoxical sleep deprivationSleep

Identifiers

PMID25707915
OpenAlexW2108100721

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.