Evidence map›Paper›PMID 35065194›Full record

ArticleBrain, behavior, and immunity2022

Sex-dependent pain trajectories induced by prolactin require an inflammatory response for pain resolution.

Jennifer Mecklenburg, Andi Wangzhou, Anahit H Hovhannisyan, Priscilla Barba-Escobedo, Sergey A Shein, Yi Zou, Korri Weldon, Zhao Lai, Vincent Goffin, Gregory Dussor and 3 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05720065 (Peripheral TMD Pain Mechanisms and the Effect by Botulinum Toxin A. A Randomized, Controlled, Double-blind Study), which is not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 12% 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.

NCT05720065 phase2recruitingnot on this mapstarted 2023, after this paper: background citation

Peripheral TMD Pain Mechanisms and the Effect by Botulinum Toxin A. A Randomized, Controlled, Double-blind Study

TypeinterventionalSponsorKarolinska InstitutetRan2023 to 2027Enrolled100ConditionsTemporomandibular DisordersArmsBotulinum toxin type A, Isotonic saline 0,9%
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 18 citations in OpenAlex.

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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

13 authors at 3 institutions in 2 countries.

Jennifer MecklenburgDepartment of Endodontics, The School of Dentistry, University of Texas Health Science Center at San Antonio (UTHSCSA), San Antonio, TX 78229, United States.
Andi WangzhouDepartment of Neuroscience and Center for Advanced Pain Studies, University of Texas at Dallas (UTD), Richardson, TX 75080, United States.
Anahit H HovhannisyanDepartment of Endodontics, The School of Dentistry, University of Texas Health Science Center at San Antonio (UTHSCSA), San Antonio, TX 78229, United States.
Priscilla Barba-EscobedoDepartment of Endodontics, The School of Dentistry, University of Texas Health Science Center at San Antonio (UTHSCSA), San Antonio, TX 78229, United States.
Sergey A SheinDepartments of Microbiology, Immunology & Molecular Genetics, the School of Medicine, UTHSCSA, San Antonio, TX 78229, United States.
Yi ZouMolecular Medicine, The School of Medicine, UTHSCSA, San Antonio, TX 78229, United States.
Korri WeldonMolecular Medicine, The School of Medicine, UTHSCSA, San Antonio, TX 78229, United States.
Zhao LaiMolecular Medicine, The School of Medicine, UTHSCSA, San Antonio, TX 78229, United States; Greehey Children's Cancer Research Institute, UTHSCSA, United States.
Vincent GoffinInserm U1151, Université Paris Descartes, Paris, France.
Gregory DussorDepartment of Neuroscience and Center for Advanced Pain Studies, University of Texas at Dallas (UTD), Richardson, TX 75080, United States.
Alexei V TumanovDepartments of Microbiology, Immunology & Molecular Genetics, the School of Medicine, UTHSCSA, San Antonio, TX 78229, United States.
Theodore J PriceDepartment of Neuroscience and Center for Advanced Pain Studies, University of Texas at Dallas (UTD), Richardson, TX 75080, United States.
Armen N AkopianDepartment of Endodontics, The School of Dentistry, University of Texas Health Science Center at San Antonio (UTHSCSA), San Antonio, TX 78229, United States; Departments of Pharmacology, The School of Medicine, UTHSCSA, San Antonio, TX 78229, United States. Electronic address: Akopian@UTHSCSA.edu.
The University of Texas Health Science Center at San Antonio · USThe University of Texas at Dallas · USUniversité Paris Cité · FR

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
Translation Control of Pain PlasticityR01NS065926 · NINDS · UNIVERSITY OF TEXAS DALLAS · PI PRICE, THEODORE J. · 2010 to 2023
$5.7M
LIGHT and Lymphotoxin targeting for the treatment of chronic orofacial pain conditionsR01DE029187 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI AKOPIAN, ARMEN N, RUPAREL, SHIVANI B · 2019 to 2021
$3.8M
Sex-specific regulation of local translation and chronic pain mechanisms in femalesR01NS102161 · NINDS · UNIVERSITY OF TEXAS DALLAS · PI AKOPIAN, ARMEN N, PRICE, THEODORE J. · 2018 to 2022
$2.5M
Lymphotoxin-Beta Receptor Peripheral Signaling Regulates the Transition to Inflammation and Neuropathy-Induced Chronic PainR01NS112263 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI AKOPIAN, ARMEN N, TUMANOV, ALEXEI V · 2020 to 2024
$2.4M
Meningeal prolactin signaling and female-selective migraine mechanismsR01NS104200 · NINDS · UNIVERSITY OF TEXAS DALLAS · PI AKOPIAN, ARMEN N, DUSSOR, GREGORY O · 2018 to 2022
$2.4M
Prolactin regulation of postoperative pain in males and femalesR01GM112747 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI AKOPIAN, ARMEN N · 2015 to 2018
$1.2M
High Throughput DNA Sequencer: Illumina HiSeq 3000 SequencerS10OD021805 · OD · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LAI, ZHAO · 2016 to 2016
$600k
NCI NIH HHS P30 CA054174NIDCR NIH HHS R01 DE029187NIGMS NIH HHS R01 GM112747NIH HHS S10 OD021805NINDS NIH HHS R01 NS065926NINDS NIH HHS R01 NS102161NINDS NIH HHS R01 NS104200NINDS NIH HHS R01 NS112263
6 · The paper itself

Abstract

Pain development and resolution patterns in many diseases are sex-dependent. This study aimed to develop pain models with sex-dependent resolution trajectories, and identify factors linked to resolution of pain in females and males. Using different intra-plantar (i.pl.) treatment protocols with prolactin (PRL), we established models with distinct, sex-dependent patterns for development and resolution of pain. An acute PRL-evoked pain trajectory, in which hypersensitivity is fully resolved within 1 day, showed substantial transcriptional changes after pain-resolution in female and male hindpaws and in the dorsal root ganglia (DRG). This finding supports the notion that pain resolution is an active process. Prolonged treatment with PRL high dose (1 μg) evoked mechanical hypersensitivity that resolved within 5-7 days in mice of both sexes and exhibited a pro-inflammatory transcriptional response in the hindpaw, but not DRG, at the time point preceding resolution. Flow cytometry analysis linked pro-inflammatory responses in female hindpaws to macrophages/monocytes, especially CD11b

Indexed as

ProlactinReceptors, ProlactinAnimalsFemaleGanglia, SpinalMaleMicePainSensory Receptor CellsProlactinReceptors, ProlactinDRGInflammationPain resolutionProlactinSex-differenceSkin

Identifiers

PMID35065194
PMCPMC9173405
OpenAlexW4206206032

What OpenQuestion holds

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Registered trials

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.