Evidence map›Paper›PMID 30785235›Full record

ArticlePhysiological reports2019

Endotoxin-induced cerebral pathophysiology: differences between fetus and newborn.

Susan Y S Feng, Jacob H Hollis, Thilini Samarasinghe, David J Phillips, Shripada Rao, Victor Y H Yu, Adrian M Walker

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

7 authors at 5 institutions in 1 country.

Susan Y S FengThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Victoria, Australia.
Jacob H HollisDepartment of Physiology, Monash University, Clayton, Victoria, Australia.
Thilini SamarasingheThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Victoria, Australia.
David J PhillipsAcademic & Medical Portfolio, Epworth HealthCare, Richmond, Victoria, Australia.
Shripada RaoNeonatal Directorate, King Edward Memorial Hospital, Perth Children's Hospital, Subiaco, Western Australia, Australia.
Victor Y H YuThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Victoria, Australia.
Adrian M WalkerThe Ritchie Centre, Hudson Institute of Medical Research, Clayton, Victoria, Australia.ORCID 0000-0001-6928-3668
Hudson Institute of Medical Research · AUPrincess Margaret Hospital for Children · AUEpworth Hospital · AUMonash Medical Centre · AUMonash University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the comparative pathophysiology of perinatal infection in the fetus and newborn is uncertain, this study contrasted the cerebral effects of endotoxemia in conscious fetal sheep and newborn lambs. Responses to intravenous bacterial endotoxin (lipopolysaccharide, LPS) or normal saline were studied on three consecutive days in fetal sheep (LPS 1 μg/kg, n = 5; normal saline n = 5) and newborn lambs (LPS 2 μg/kg, n = 10; normal saline n = 5). Cerebro-vascular function was assessed by monitoring cerebral blood flow (CBF) and cerebral vascular resistance (CVR) over 12 h each day, and inflammatory responses were assessed by plasma TNF alpha (TNF-α), nitrate and nitrite concentrations. Brain injury was quantified by counting both resting and active macrophages in the caudate nucleus and periventricular white matter (PVWM). An acute cerebral vasoconstriction (within 1 h of LPS injection) occurred in both the fetus (ΔCVR +53%) and newborn (ΔCVR +63%); subsequently prolonged cerebral vasodilatation occurred in the fetus (ΔCVR -33%) in association with double plasma nitrate/nitrite concentrations, but not in the newborn. Abundant infiltration of activated macrophages was observed in both CN and PVWM at each age, with the extent being 2-3 times greater in the fetus (P < 0.001). In conclusion, while the fetus and newborn experience a similar acute disruption of the cerebral circulation after LPS, the fetus suffers a more prolonged circulatory disruption, a greater infiltration of activated macrophages, and an exaggerated susceptibility to brain injury.

Indexed as

AnimalsBrainCerebrovascular CirculationEncephalitisFemaleFetal DiseasesLipopolysaccharidesMacrophagesMaleNitratesNitritesSheepTumor Necrosis Factor-alphaVasoconstrictionVasodilationLipopolysaccharidesNitratesNitritesTumor Necrosis Factor-alphaBrainendotoxinfetusinjurynewborn

Identifiers

PMID30785235
PMCPMC6381816
OpenAlexW2917325474

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.