Evidence map›Paper›PMID 26661194›Full record

ArticleJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism2016

Immediate remote ischemic postconditioning after hypoxia ischemia in piglets protects cerebral white matter but not grey matter.

Mojgan Ezzati, Alan Bainbridge, Kevin D Broad, Go Kawano, Aaron Oliver-Taylor, Eridan Rocha-Ferreira, Daniel Alonso-Alconada, Igor Fierens, Jamshid Rostami, K Jane Hassell and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
6.9field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
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  11. Perinatal hypoxic-ischemic brain injury in large animal models: Relevance to human neonatal encephalopathy.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2018
    Review
  12. Article
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  15. Molecular Bases of Brain Preconditioning.Frontiers in neuroscience · 2017
    Article
  16. Article
  17. 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

20 authors at 6 institutions in 3 countries.

Mojgan EzzatiInstitute for Women's Health, University College London, London, UK.
Alan BainbridgePhysics and Bioengineering, University College London NHS Trust, London, UK.
Kevin D BroadInstitute for Women's Health, University College London, London, UK.
Go KawanoInstitute for Women's Health, University College London, London, UK.
Aaron Oliver-TaylorInstitute for Women's Health, University College London, London, UK.
Eridan Rocha-FerreiraInstitute for Women's Health, University College London, London, UK.
Daniel Alonso-AlconadaInstitute for Women's Health, University College London, London, UK.
Igor FierensInstitute for Women's Health, University College London, London, UK.
Jamshid RostamiInstitute for Women's Health, University College London, London, UK.
K Jane HassellInstitute for Women's Health, University College London, London, UK.
Ilias TachtsidisMedical Physics and Biomedical Engineering, University College London, London, UK.
Pierre GressensDepartment of Perinatal Imaging and Health, Division of Imaging Sciences and Biomedical Engineering, King's College London, King's Health Partners, St. Thomas' Hospital, London, UK Inserm, U1141, Paris, France University Paris Diderot, Sorbonne Paris Cité, Paris, France PremUP, Paris, France.
Mariya HristovaInstitute for Women's Health, University College London, London, UK.
Kate BennettInstitute for Women's Health, University College London, London, UK.
Sophie LebonPremUP, Paris, France.
Bobbi FleissDepartment of Perinatal Imaging and Health, Division of Imaging Sciences and Biomedical Engineering, King's College London, King's Health Partners, St. Thomas' Hospital, London, UK Inserm, U1141, Paris, France University Paris Diderot, Sorbonne Paris Cité, Paris, France PremUP, Paris, France.
Derek YellonThe Hatter Cardiovascular Institute, University College London, London, UK.
Derek J HausenloyThe Hatter Cardiovascular Institute, University College London, London, UK Cardiovascular and Metabolic Disorders Program, Duke-NUS Graduate Medical School, Singapore, Singapore National Heart Centre Singapore, Singapore.
Xavier GolayInstitute of Neurology, University College London, London, UK.
Nicola J RobertsonInstitute for Women's Health, University College London, London, UK n.robertson@ucl.ac.uk.
University College London · GBLondon Women's Clinic · GBCentre de Recherche de l'Institut de Démographie de l'Université Paris 1 · FRDuke-NUS Medical School · SGInserm · FRUniversité Paris Cité · FR

Funding

Medical Research Council MR/J00457X/1Wellcome Trust 104580
6 · The paper itself

Abstract

Remote ischemic postconditioning (RIPostC) is a promising therapeutic intervention whereby brief episodes of ischemia/reperfusion of one organ (limb) mitigate damage in another organ (brain) that has experienced severe hypoxia-ischemia. Our aim was to assess whether RIPostC is protective following cerebral hypoxia-ischemia in a piglet model of neonatal encephalopathy (NE) using magnetic resonance spectroscopy (MRS) biomarkers and immunohistochemistry. After hypoxia-ischemia (HI), 16 Large White female newborn piglets were randomized to: (i) no intervention (n = 8); (ii) RIPostC - with four, 10-min cycles of bilateral lower limb ischemia/reperfusion immediately after HI (n = 8). RIPostC reduced the hypoxic-ischemic-induced increase in white matter proton MRS lactate/N acetyl aspartate (p = 0.005) and increased whole brain phosphorus-31 MRS ATP (p = 0.039) over the 48 h after HI. Cell death was reduced with RIPostC in the periventricular white matter (p = 0.03), internal capsule (p = 0.002) and corpus callosum (p = 0.021); there was reduced microglial activation in corpus callosum (p = 0.001) and more surviving oligodendrocytes in corpus callosum (p = 0.029) and periventricular white matter (p = 0.001). Changes in gene expression were detected in the white matter at 48 h, including KATP channel and endothelin A receptor. Immediate RIPostC is a potentially safe and promising brain protective therapy for babies with NE with protection in white but not grey matter.

Indexed as

Adenosine TriphosphateAnimalsAnimals, NewbornAspartic AcidBiomarkersBrain MappingDisease Models, AnimalElectroencephalographyGene ExpressionGray MatterHypoxia-Ischemia, BrainImmunohistochemistryIschemic PostconditioningKATP ChannelsLactic AcidLower ExtremityAdenosine TriphosphateAspartic AcidBiomarkersKATP ChannelsLactic AcidN-acetylaspartateReceptor, Endothelin ABirth asphyxiahypoxia–ischemianeonatal encephalopathyneuroprotectionremote ischemic postconditioning

Identifiers

PMID26661194
PMCPMC4976661
OpenAlexW2291734176

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.