Evidence map›Paper›PMID 23994182›Full record

ArticleNeuroscience2013

Sex-dependent roles of prolactin and prolactin receptor in postoperative pain and hyperalgesia in mice.

M J Patil, D P Green, M A Henry, A N Akopian

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Prolactin and pain of endometriosis.Pharmacology & therapeutics · 2023
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Endorphins, Sexuality, and Reproduction.Advances in neurobiology · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. A Female-Specific Role for Calcitonin Gene-Related Peptide (CGRP) in Rodent Pain Models.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

4 authors at 2 institutions in 1 country.

M J PatilDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, TX 78229, USA.
D P Green
M A Henry
A N Akopian
American Association of Endodontists · USThe University of Texas Health Science Center at San Antonio · US

Funding

Prolactin Regulation of Trigeminal NociceptorsR01DE017696 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI AKOPIAN, ARMEN N · 2007 to 2011
$1.8M
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
The Role of the OLAM System in Burn PainF31NS082019 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI GREEN, DUSTIN PEPPER · 2013 to 2014
$53k
NIDCR NIH HHS R01 DE017696NIGMS NIH HHS R01 GM112747NINDS NIH HHS F31 NS082019
6 · The paper itself

Abstract

Although surgical trauma activates the anterior pituitary gland and elicits an increase in prolactin (PRL) serum levels that can modulate nociceptive responses, the role of PRL and the PRL-receptor (PRL-R) in thermal and mechanical hyperalgesia in postoperative pain is unknown. Acute postoperative pain condition was generated with the use of the hindpaw plantar incision model. Results showed endogenous PRL levels were significantly increased in serum, operated hindpaw and spinal cords of male and female rats 24h after incision. These alterations were especially pronounced in females. We then examined the role of the PRL system in thermal and mechanical hyperalgesia in male and female mice 3-168 h after plantar incision with the use of knock-out (KO) mice with PRL or PRL-R gene ablations and in wild-type (WT) mice. WT mice showed postoperative cold hyperalgesia in a sex-dependent manner (only in females), but with no effect on heat hyperalgesia or mechanical allodynia in either sex. Studies in KO mice showed no effect of PRL and PRL-R gene ablation on heat and cold hyperalgesia in male mice, while heat hyperlgesia were reduced 3-72 h post-surgery in female PRL and PRL-R KO mice. In contrast, PRL and PRL-R ablations significantly attenuated mechanical allodynia 3-72 h post-surgery in both male and female mice. Overall, we found elevated PRL levels in serum, hindpaws and spinal cords after incision, and identify a contributory role for the PRL system in postoperative pain responses to thermal stimuli in females and to mechanical stimuli in both males and females.

Indexed as

Analysis of VarianceAnimalsDisease Models, AnimalFemaleFunctional LateralityHyperalgesiaMaleMiceMice, KnockoutPain MeasurementPain ThresholdPhysical StimulationPostoperative PainProlactinRatsReceptors, ProlactinProlactinReceptors, Prolactinanalysis of varianceANOVAknock-outKOpainpost operative modelPRLPRL KOPRL null-mutantPRL-RPRL-receptorPRL-R KOPRL-R null-mutantprolactinprolactin receptorsex-dependencewild-typeWT

Identifiers

PMID23994182
PMCPMC4943227
OpenAlexW2030262806

What OpenQuestion holds

Textmetadata
LicenceTDM
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.