Evidence map›Paper›PMID 37635256›Full record

ArticleCell & bioscience2023

Repetitive and compulsive behavior after Early-Life-Pain associated with reduced long-chain sphingolipid species.

Alexandra Vogel, Timo Ueberbach, Annett Wilken-Schmitz, Lisa Hahnefeld, Luisa Franck, Marc-Philipp Weyer, Tassilo Jungenitz, Tobias Schmid, Giulia Buchmann, Florian Freudenberg and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell & bioscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Dysregulation of sphingolipid metabolism in pain.Frontiers in pharmacology · 2024
    Review
  5. Article
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

16 authors at 2 institutions in 1 country.

Alexandra VogelInstitute of Clinical Pharmacology, Faculty of Medicine, Goethe-University, Frankfurt, Germany.
Timo UeberbachInstitute of Physiology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Annett Wilken-SchmitzInstitute of Clinical Pharmacology, Faculty of Medicine, Goethe-University, Frankfurt, Germany.
Lisa HahnefeldInstitute of Clinical Pharmacology, Faculty of Medicine, Goethe-University, Frankfurt, Germany.
Luisa FranckInstitute of Clinical Pharmacology, Faculty of Medicine, Goethe-University, Frankfurt, Germany.
Marc-Philipp WeyerInstitute of Clinical Pharmacology, Faculty of Medicine, Goethe-University, Frankfurt, Germany.
Tassilo JungenitzInstitute of Clinical Neuroanatomy, Neuroscience Center, Goethe University, Frankfurt, Germany.
Tobias SchmidInstitute of Biochemistry I, Faculty of Medicine, Goethe-University, Frankfurt, Germany.
Giulia BuchmannInstitute of Cardiovascular Physiology, Faculty of Medicine, Goethe-University, Frankfurt, Germany.
Florian FreudenbergDepartment of Psychiatry, Psychosomatic Medicine and Psychotherapy, Goethe-University Hospital, Frankfurt, Germany.
Ralf P BrandesInstitute of Cardiovascular Physiology, Faculty of Medicine, Goethe-University, Frankfurt, Germany.
Robert GurkeInstitute of Clinical Pharmacology, Faculty of Medicine, Goethe-University, Frankfurt, Germany.
Stephan W SchwarzacherInstitute of Clinical Neuroanatomy, Neuroscience Center, Goethe University, Frankfurt, Germany.
Gerd GeisslingerInstitute of Clinical Pharmacology, Faculty of Medicine, Goethe-University, Frankfurt, Germany.
Thomas MittmannInstitute of Physiology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Irmgard TegederInstitute of Clinical Pharmacology, Faculty of Medicine, Goethe-University, Frankfurt, Germany. itegeder@hotmail.com.ORCID http://orcid.org/0000-0001-7524-8025
Goethe University Frankfurt · DEJohannes Gutenberg University Mainz · DE

Funding

Deutsche Forschungsgemeinschaft 445757098Deutsche Forschungsgemeinschaft CRC1039 A03Deutsche Forschungsgemeinschaft CRC1039 Z01Deutsche Forschungsgemeinschaft CRC1080 C02
6 · The paper itself

Abstract

backgroundPain in early life may impact on development and risk of chronic pain. We developed an optogenetic Cre/loxP mouse model of "early-life-pain" (ELP) using mice with transgenic expression of channelrhodopsin-2 (ChR2) under control of the Advillin (Avil) promoter, which drives expression of transgenes predominantly in isolectin B4 positive non-peptidergic nociceptors in postnatal mice. Avil-ChR2 (Cre +) and ChR2-flfl control mice were exposed to blue light in a chamber once daily from P1-P5 together with their Cre-negative mother.

resultsELP caused cortical hyperexcitability at P8-9 as assessed via multi-electrode array recordings that coincided with reduced expression of synaptic genes (RNAseq) including Grin2b, neurexins, piccolo and voltage gated calcium and sodium channels. Young adult (8-16 wks) Avil-ChR2 mice presented with nociceptive hypersensitivity upon heat or mechanical stimulation, which did not resolve up until one year of age. The persistent hypersensitivy to nociceptive stimuli was reflected by increased calcium fluxes in primary sensory neurons of aged mice (1 year) upon capsaicin stimulation. Avil-ChR2 mice behaved like controls in maze tests of anxiety, social interaction, and spatial memory but IntelliCage behavioral studies revealed repetitive nosepokes and corner visits and compulsive lickings. Compulsiveness at the behavioral level was associated with a reduction of sphingomyelin species in brain and plasma lipidomic studies. Behavioral studies were done with female mice.

conclusionThe results suggest that ELP may predispose to chronic "pain" and compulsive psychopathology in part mediated by alterations of sphingolipid metabolism, which have been previously described in the context of addiction and psychiatric diseases.

Indexed as

CalciumCompulsive behaviorCortical excitabilityIntelliCageMultichannel electrode arraysNociceptionOptogeneticRepetitiveness

Identifiers

PMID37635256
PMCPMC10463951
OpenAlexW4386203998

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.