Evidence map›Paper›PMID 29464766›Full record

ArticleJournal of pineal research2018

Systemic and transdermal melatonin administration prevents neuropathology in response to perinatal asphyxia in newborn lambs.

James D S Aridas, Tamara Yawno, Amy E Sutherland, Ilias Nitsos, Michael Ditchfield, Flora Y Wong, Rod W Hunt, Michael C Fahey, Atul Malhotra, Euan M Wallace and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of pineal research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
12.7field-weighted citation impact, top 1% 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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 57 citations in OpenAlex.

  1. Melatonin treatment for neonatal encephalopathy.The Cochrane database of systematic reviews · 2026
    Pooled it
  2. Efficacy of melatonin in term neonatal models of perinatal hypoxia-ischaemia.Annals of clinical and translational neurology · 2022
    Pooled it
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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

12 authors at 3 institutions in 1 country.

James D S AridasThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Vic., Australia.ORCID http://orcid.org/0000-0002-4000-2110
Tamara YawnoThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Vic., Australia.
Amy E SutherlandThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Vic., Australia.
Ilias NitsosThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Vic., Australia.
Michael DitchfieldMonash Children's Hospital, Monash Health, Clayton, Vic., Australia.
Flora Y WongThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Vic., Australia.
Rod W HuntMurdoch Children's Research Institute, Melbourne, Vic., Australia.
Michael C FaheyThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Vic., Australia.
Atul MalhotraThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Vic., Australia.
Euan M WallaceThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Vic., Australia.ORCID http://orcid.org/0000-0002-4506-5233
Graham JenkinThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Vic., Australia.
Suzanne L MillerThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Vic., Australia.
Hudson Institute of Medical Research · AUMonash Children’s Hospital · AUMurdoch Children's Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Perinatal asphyxia remains a principal cause of infant mortality and long-term neurological morbidity, particularly in low-resource countries. No neuroprotective interventions are currently available. Melatonin (MLT), a potent antioxidant, anti-inflammatory and antiapoptotic agent, offers promise as an intravenous (IV) or transdermal therapy to protect the brain. We aimed to determine the effect of melatonin (IV or transdermal patch) on neuropathology in a lamb model of perinatal asphyxia. Asphyxia was induced in newborn lambs via umbilical cord occlusion at birth. Animals were randomly allocated to melatonin commencing 30 minutes after birth (60 mg in 24 hours; IV or transdermal patch). Brain magnetic resonance spectroscopy (MRS) was undertaken at 12 and 72 hours. Animals (control n = 9; control+MLT n = 6; asphyxia n = 16; asphyxia+MLT [IV n = 14; patch n = 4]) were euthanised at 72 hours, and cerebrospinal fluid (CSF) and brains were collected for analysis. Asphyxia resulted in severe acidosis (pH 6.9 ± 0.0; lactate 9 ± 2 mmol/L) and altered determinants of encephalopathy. MRS lactate:N-acetyl aspartate ratio was 2.5-fold higher in asphyxia lambs compared with controls at 12 hours and 3-fold higher at 72 hours (P < .05). Melatonin prevented this rise (3.5-fold reduced vs asphyxia; P = .02). Asphyxia significantly increased brain white and grey matter apoptotic cell death (activated caspase-3), lipid peroxidation (4HNE) and neuroinflammation (IBA-1). These changes were significantly mitigated by both IV and patch melatonin. Systemic or transdermal neonatal melatonin administration significantly reduces the neuropathology and encephalopathy signs associated with perinatal asphyxia. A simple melatonin patch, administered soon after birth, may improve outcome in infants affected by asphyxia, especially in low-resource settings.

Indexed as

AnimalsAnimals, NewbornAsphyxia NeonatorumBrainMelatoninNeuroprotective AgentsRandom AllocationSheepMelatoninNeuroprotective Agentsbrain injurycell deathmelatoninneuroprotectionoxidative stressperinatal asphyxiaradiologytransdermal

Identifiers

PMID29464766
PMCPMC5947141
OpenAlexW2794122143

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.