Evidence map›Paper›PMID 31333645›Full record

ArticleFrontiers in immunology2019

Neonatal Intermittent Hypoxia Induces Lasting Sex-Specific Augmentation of Rat Microglial Cytokine Expression.

Elizabeth A Kiernan, Tao Wang, Amanda M Vanderplow, Sneha Cherukuri, Michael E Cahill, Jyoti J Watters

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Perinatal Hypoxemia and Oxygen Sensing.Comprehensive Physiology · 2021
    Article
  8. Article
  9. Article
  10. Review
  11. 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

6 authors at 1 institution in 1 country.

Elizabeth A KiernanNeuroscience Training Program, University of Wisconsin-Madison, Madison, WI, United States.
Tao WangDepartment of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI, United States.
Amanda M VanderplowDepartment of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI, United States.
Sneha CherukuriDepartment of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI, United States.
Michael E CahillNeuroscience Training Program, University of Wisconsin-Madison, Madison, WI, United States.
Jyoti J WattersNeuroscience Training Program, University of Wisconsin-Madison, Madison, WI, United States.
University of Wisconsin–Madison · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AMY TRENTHAM-DIETZ · 1985 to 2026
$142.6M
NEUROSCIENCE TRAINING PROGRAMT32GM007507 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI HALLORAN, MARY C · 1985 to 2017
$9.3M
Intermittent Hypoxia-Induced Inflammation Modulates Respiratory PlasticityR01HL111598 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI MITCHELL, GORDON S., WATTERS, JYOTI J · 2012 to 2016
$2.9M
Regulation of microglial plasticity by TLR4 and microRNAsR01NS085226 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI WATTERS, JYOTI J · 2015 to 2019
$1.7M
Special BD LSR FortessaS10OD018202 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI PATANKAR, MANISH S · 2014 to 2014
$351k
Oligosaccharides Regulating Cell FunctionR21GM075007 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SASISEKHARAN, RAM · 2005 to 2006
$226k
The Role of TLR4 Signaling and Histone Modifications in Neonatal Microglial Priming by Chronic Intermittent HypoxiaF31NS100229 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI KIERNAN, ELIZABETH ANNE · 2017 to 2019
$62k
MOLECULAR MECHANISMS OF ESTROGEN INDUCED CELL GROWTHF32CA081733 · NCI · UNIVERSITY OF WISCONSIN MADISON · PI WATTERS, JYOTI J · 1999 to 2000
$38k
NCI NIH HHS F32 CA081733NCI NIH HHS P30 CA014520NHLBI NIH HHS R01 HL111598NIGMS NIH HHS R21 GM075007NIGMS NIH HHS T32 GM007507NIH HHS S10 OD018202NINDS NIH HHS F31 NS100229NINDS NIH HHS R01 NS085226
6 · The paper itself

Abstract

Sleep disordered breathing (SDB) affects 3-5% of the pediatric population, including neonates who are highly susceptible due to an underdeveloped ventilatory control system, and REM-dominated sleep. Although pediatric SDB is associated with poor cognitive outcomes, very little research has focused on models of pediatric SDB, particularly in neonates. In adults and neonates, intermittent hypoxia (IH), a hallmark of SDB, recapitulates multiple physiological aspects of severe SDB, including neuronal apoptosis, sex-specific cognitive deficits, and neuroinflammation. Microglia, resident CNS immune cells, are important mediators of neurodevelopment and neuroinflammation, but to date, no studies have examined the molecular properties of microglia in the context of neonatal IH. Here, we tested the hypothesis that neonatal IH will enhance microglial inflammation and sex-specifically lead to long-term changes in working memory. To test this hypothesis, we exposed post-natal day (P1) neonates with dams to an established adult model of pathological IH consisting of 2 min cycles of 10.5% O

Indexed as

AnimalsAnimals, NewbornCytokinesDisease Models, AnimalFemaleHypoxiaInflammationLipopolysaccharidesMaleMaze LearningMemory, Short-TermMicrogliaRatsRats, Sprague-DawleyRNA-SeqSex FactorsCytokinesLipopolysaccharidesdevelopmentintermittent hypoxiamicroglianeonatesex differences

Identifiers

PMID31333645
PMCPMC6615134
OpenAlexW2949725531

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.