Evidence map›Paper›PMID 22721955›Full record

ArticleEpilepsy research2012

Factors affecting outcomes of pilocarpine treatment in a mouse model of temporal lobe epilepsy.

Paul S Buckmaster, Megan M Haney

Abstract read
In one paragraph

Article in Epilepsy research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

28 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
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  3. Article
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  6. Adaptive Mossy Cell Circuit Plasticity after Status Epilepticus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
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  8. Review
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  12. Review
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  16. Article
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  19. Increased expression of vascular endothelial growth factor-C and vascular endothelial growth factor receptor-3 after pilocarpine-induced status epilepticus in mice.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2019
    Article
  20. 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

2 authors at 1 institution in 1 country.

Paul S BuckmasterDepartment of Comparative Medicine, Stanford University, Stanford, CA 94305, United States. psb@stanford.edu
Megan M Haney
Stanford University · US

Funding

Ictogenesis in a model of temporal lobe epilepsyR01NS040276 · NINDS · STANFORD UNIVERSITY · PI BUCKMASTER, PAUL S. · 2000 to 2019
$5.8M
INTERNEURON BASED MECHANISMS OF TEMPORAL LOBE EPILEPSYR01NS039110 · NINDS · STANFORD UNIVERSITY · PI BUCKMASTER, PAUL S. · 2000 to 2014
$4.8M
Epilepsy Research ProgramP01NS012151 · NINDS · STANFORD UNIVERSITY · PI HUGUENARD, JOHN R · 2008 to 2011
$4.4M
Research Opportunities in Comparative MedicineT35OD010989 · OD · STANFORD UNIVERSITY · PI BUCKMASTER, PAUL S. · 2012 to 2022
$565k
RESEARCH OPPORTUNITIES IN COMPARATIVE MEDICINET35RR017188 · NCRR · STANFORD UNIVERSITY · PI BUCKMASTER, PAUL S. · 2002 to 2011
$379k
NCRR NIH HHS T35 RR017188NIH HHS T35 OD010989NINDS NIH HHS P01 NS012151NINDS NIH HHS R01 NS039110NINDS NIH HHS R01 NS040276
6 · The paper itself

Abstract

Pilocarpine-treated mice are an increasingly used model of temporal lobe epilepsy. However, outcomes of treatment can be disappointing, because many mice die or fail to develop status epilepticus. To improve animal welfare and outcomes of future experiments we analyzed results of previous pilocarpine treatments to identify factors that correlate with development of status epilepticus and survival. All treatments were performed by one investigator with mice of the FVB background strain. Results from 2413 mice were evaluated for effects of sex, age, body weight, and latency between administration of atropine methyl bromide and pilocarpine. All parameters correlated with effects on outcomes. Best results were obtained from male mice, 6-7 weeks old, and 21-25 g, with pilocarpine administered 18-30 min after atropine methyl bromide. In that group only 23% failed to develop status epilepticus, and 64% developed status epilepticus and survived. Those results are substantially better than that of the total sample in which 31% failed to develop status epilepticus and only 34% developed status epilepticus and survived.

Indexed as

Age FactorsAnimalsAnticonvulsantsAtropineBody WeightDiazepamDisease Models, AnimalEpilepsy, Temporal LobeFemaleGlutamate DecarboxylaseGreen Fluorescent ProteinsMaleMiceMice, TransgenicMuscarinic AgonistsMuscarinic AntagonistsAnticonvulsantsAtropineDiazepamGlutamate Decarboxylaseglutamate decarboxylase 1Green Fluorescent ProteinsMuscarinic AgonistsMuscarinic AntagonistsPilocarpine

Identifiers

PMID22721955
PMCPMC3458129
OpenAlexW2117981682

What OpenQuestion holds

Textmetadata
LicenceTDM
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.