Evidence map›Paper›PMID 34625655›Full record

ArticlePediatric research2022

Azithromycin reduces inflammation-amplified hypoxic-ischemic brain injury in neonatal rats.

John D E Barks, Yiqing Liu, Ian A Dopp, Faye S Silverstein

Open access · greenAbstract read
In one paragraph

Article in Pediatric research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

14 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

4 authors at 1 institution in 1 country.

John D E BarksDepartment of Pediatrics, University of Michigan Medical School, The University of Michigan, Ann Arbor, MI, USA. jbarks@med.umich.edu.ORCID http://orcid.org/0000-0003-1320-905X
Yiqing LiuDepartment of Pediatrics, University of Michigan Medical School, The University of Michigan, Ann Arbor, MI, USA.
Ian A DoppDepartment of Pediatrics, University of Michigan Medical School, The University of Michigan, Ann Arbor, MI, USA.
Faye S SilversteinDepartment of Pediatrics, University of Michigan Medical School, The University of Michigan, Ann Arbor, MI, USA.
University of Michigan · US

Funding

Michigan Institute for Clinical and Health Research (MICHR)UL1TR002240 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUMENG, JULIE C, MASHOUR, GEORGE ALEXANDER · 2017 to 2022
$54.9M
Repurposing Azithromycin for Neonatal NeuroprotectionR21HD096251 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BARKS, JOHN D · 2018 to 2019
$429k
NCATS NIH HHS UL1 TR002240NICHD NIH HHS R21 HD096251
6 · The paper itself

Abstract

backgroundSystemic inflammation amplifies neonatal hypoxic-ischemic (HI) brain injury. Azithromycin (AZ), an antibiotic with anti-inflammatory properties, improves sensorimotor function and reduces tissue damage after neonatal rat HI brain injury. The objective of this study was to determine if AZ is neuroprotective in two neonatal rat models of inflammation-amplified HI brain injury. DESIGN/

methodsSeven-day-old (P7) rats received injections of toll-like receptor agonists lipopolysaccharide (LPS) or Pam

resultsIn both LPS + HI and PAM + HI models, AZ improved sensorimotor function, survival, brain tissue preservation, and composite scores. Benefits increased with five- vs. three-dose AZ and declined with longer initiation delay.

conclusionsPerinatal systemic infection is a common comorbidity of neonatal asphyxia brain injury and contributes to adverse outcomes. These data support further evaluation of AZ as a candidate treatment for neonatal neuroprotection. IMPACT: AZ treatment decreases sensorimotor impairment and severity of brain injury, and improves survival, after inflammation-amplified HI brain injury, and this can be achieved even with a 2 h delay in initiation. This neuroprotective benefit is seen in models of inflammation priming by both Gram-negative and Gram-positive infections. This extends our previous findings that AZ treatment is neuroprotective after HI brain injury in neonatal rats.

Indexed as

Brain InjuriesHypoxia-Ischemia, BrainNeuroprotective AgentsAnimalsAnimals, NewbornAnti-Bacterial AgentsAnti-Inflammatory AgentsAzithromycinBrainInflammationLipopolysaccharidesOxygenRatsRats, WistarToll-Like ReceptorsAnti-Bacterial AgentsAnti-Inflammatory AgentsAzithromycinLipopolysaccharidesNeuroprotective AgentsOxygenToll-Like Receptors

Identifiers

PMID34625655
PMCPMC8989723
OpenAlexW3203389190

What OpenQuestion holds

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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.