Evidence map›Paper›PMID 29294386›Full record

ArticleNeuroImage2018

Seizure epicenter depth and translaminar field potential synchrony underlie complex variations in tissue oxygenation during ictal initiation.

Samuel S Harris, Luke W Boorman, Aneurin J Kennerley, Paul S Sharp, Chris Martin, Peter Redgrave, Theodore H Schwartz, Jason Berwick

Open access · hybridAbstract read
In one paragraph

Article in NeuroImage, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Differential contribution of excitatory and inhibitory neurons in shaping neurovascular coupling in different epileptic neural states.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
  3. Article
  4. Article
  5. 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

8 authors at 2 institutions in 2 countries.

Samuel S HarrisDepartment of Psychology, Neurovascular and Neuroimaging Research Group, University of Sheffield, Sheffield S10 2TN, UK. Electronic address: sam.harris@sheffield.ac.uk.
Luke W BoormanDepartment of Psychology, Neurovascular and Neuroimaging Research Group, University of Sheffield, Sheffield S10 2TN, UK.
Aneurin J KennerleyDepartment of Psychology, Neurovascular and Neuroimaging Research Group, University of Sheffield, Sheffield S10 2TN, UK.
Paul S SharpDepartment of Psychology, Neurovascular and Neuroimaging Research Group, University of Sheffield, Sheffield S10 2TN, UK.
Chris MartinDepartment of Psychology, Neurovascular and Neuroimaging Research Group, University of Sheffield, Sheffield S10 2TN, UK.
Peter RedgraveDepartment of Psychology, Neurovascular and Neuroimaging Research Group, University of Sheffield, Sheffield S10 2TN, UK.
Theodore H SchwartzDepartment of Neurological Surgery, Brain and Mind Research Institute, Brain and Spine Center, Weill Cornell Medical College, New York Presbyterian Hospital, 525 East 68th Street, Box 99, New York, NY 10021, USA.
Jason BerwickDepartment of Psychology, Neurovascular and Neuroimaging Research Group, University of Sheffield, Sheffield S10 2TN, UK.
University of Sheffield · GBNewYork–Presbyterian Hospital · US

Funding

Medical Research Council MR/M013553/1
6 · The paper itself

Abstract

Whether functional hyperemia during epileptic activity is adequate to meet the heightened metabolic demand of such events is controversial. Whereas some studies have demonstrated hyperoxia during ictal onsets, other work has reported transient hypoxic episodes that are spatially dependent on local surface microvasculature. Crucially, how laminar differences in ictal evolution can affect subsequent cerebrovascular responses has not been thus far investigated, and is likely significant in view of possible laminar-dependent neurovascular mechanisms and angioarchitecture. We addressed this open question using a novel multi-modal methodology enabling concurrent measurement of cortical tissue oxygenation, blood flow and hemoglobin concentration, alongside laminar recordings of neural activity, in a urethane anesthetized rat model of recurrent seizures induced by 4-aminopyridine. We reveal there to be a close relationship between seizure epicenter depth, translaminar local field potential (LFP) synchrony and tissue oxygenation during the early stages of recurrent seizures, whereby deep layer seizures are associated with decreased cross laminar synchrony and prolonged periods of hypoxia, and middle layer seizures are accompanied by increased cross-laminar synchrony and hyperoxia. Through comparison with functional activation by somatosensory stimulation and graded hypercapnia, we show that these seizure-related cerebrovascular responses occur in the presence of conserved neural-hemodynamic and blood flow-volume coupling. Our data provide new insights into the laminar dependency of seizure-related neurovascular responses, which may reconcile inconsistent observations of seizure-related hypoxia in the literature, and highlight a potential layer-dependent vulnerability that may contribute to the harmful effects of clinical recurrent seizures. The relevance of our findings to perfusion-related functional neuroimaging techniques in epilepsy are also discussed.

Indexed as

AnimalsBrainCerebrovascular CirculationFemaleHemodynamicsHyperoxiaRatsSeizuresHypoxiaNeurovascularSeizuresSynchrony

Identifiers

PMID29294386
PMCPMC5883323
OpenAlexW2951938538

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.