Evidence map›Paper›PMID 26630670›Full record

ArticlePloS one2015

Early-Onset Convulsive Seizures Induced by Brain Hypoxia-Ischemia in Aging Mice: Effects of Anticonvulsive Treatments.

Justin Wang, Chiping Wu, Jessie Peng, Nisarg Patel, Yayi Huang, Xiaoxing Gao, Salman Aljarallah, James H Eubanks, Robert McDonald, Liang Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  4. Between life and death: the brain twilight zones.Frontiers in neuroscience · 2023
    Review
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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

10 authors at 3 institutions in 2 countries.

Justin WangToronto Western Research Institute, University Health Network, Toronto, Ontario, Canada.
Chiping WuToronto Western Research Institute, University Health Network, Toronto, Ontario, Canada.
Jessie PengToronto Western Research Institute, University Health Network, Toronto, Ontario, Canada.
Nisarg PatelToronto Western Research Institute, University Health Network, Toronto, Ontario, Canada.
Yayi HuangToronto Western Research Institute, University Health Network, Toronto, Ontario, Canada.
Xiaoxing GaoToronto Western Research Institute, University Health Network, Toronto, Ontario, Canada.
Salman AljarallahToronto Western Research Institute, University Health Network, Toronto, Ontario, Canada.
James H EubanksToronto Western Research Institute, University Health Network, Toronto, Ontario, Canada.
Robert McDonaldDepartment of Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada.
Liang ZhangToronto Western Research Institute, University Health Network, Toronto, Ontario, Canada.
University Health Network · CAUniversity of Lethbridge · CAUniversity of Toronto · CA

Funding

Canadian Institutes of Health Research 219171
6 · The paper itself

Abstract

Aging is associated with an increased risk of seizures/epilepsy. Stroke (ischemic or hemorrhagic) and cardiac arrest related brain injury are two major causative factors for seizure development in this patient population. With either etiology, seizures are a poor prognostic factor. In spite of this, the underlying pathophysiology of seizure development is not well understood. In addition, a standardized treatment regimen with anticonvulsants and outcome assessments following treatment has yet to be established for these post-ischemic seizures. Previous studies have modeled post-ischemic seizures in adult rodents, but similar studies in aging/aged animals, a group that mirrors a higher risk elderly population, remain sparse. Our study therefore aimed to investigate early-onset seizures in aging animals using a hypoxia-ischemia (HI) model. Male C57 black mice 18-20-month-old underwent a unilateral occlusion of the common carotid artery followed by a systemic hypoxic episode (8% O2 for 30 min). Early-onset seizures were detected using combined behavioral and electroencephalographic (EEG) monitoring. Brain injury was assessed histologically at different times post HI. Convulsive seizures were observed in 65% of aging mice post-HI but not in control aging mice following either sham surgery or hypoxia alone. These seizures typically occurred within hours of HI and behaviorally consisted of jumping, fast running, barrel-rolling, and/or falling (loss of the righting reflex) with limb spasms. No evident discharges during any convulsive seizures were seen on cortical-hippocampal EEG recordings. Seizure development was closely associated with acute mortality and severe brain injury on brain histological analysis. Intra-peritoneal injections of lorazepam and fosphenytoin suppressed seizures and improved survival but only when applied prior to seizure onset and not after. These findings together suggest that seizures are a major contributing factor to acute mortality in aging mice following severe brain ischemia and that early anticonvulsive treatment may prevent seizure genesis and improve overall outcomes.

Indexed as

Age of OnsetAgingAnimalsAnticonvulsantsCerebral CortexDisease Models, AnimalHippocampusHypoxia-Ischemia, BrainInjections, IntraperitonealLorazepamMaleMiceMice, Inbred C57BLPhenytoinSeizuresAnticonvulsantsfosphenytoinLorazepamPhenytoin

Identifiers

PMID26630670
PMCPMC4668036
OpenAlexW2185125703

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.