Evidence map›Paper›PMID 25769812›Full record

ArticleNeurobiology of disease2015

Seizure-related regulation of GABAA receptors in spontaneously epileptic rats.

Marco I González, Heidi L Grabenstatter, Christian A Cea-Del Rio, Yasmin Cruz Del Angel, Jessica Carlsen, Rick P Laoprasert, Andrew M White, Molly M Huntsman, Amy Brooks-Kayal

Abstract read
In one paragraph

Article in Neurobiology of disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Clptm1, a new target in suppressing epileptic seizure by regulating GABAThe Kaohsiung journal of medical sciences · 2023
    Article
  3. Virally-induced expression of GABAProgress in neurobiology · 2022
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Neurosteroid regulation of GABABrain research · 2019
    Review
  10. Article
  11. Article
  12. Investigations in GABANeurology · 2017
    Article
  13. Article
  14. 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

9 authors.

Marco I GonzálezDepartment of Pediatrics, Division of Neurology, University of Colorado School of Medicine, Aurora, CO, 80045 USA; Translational Epilepsy Research Program, University of Colorado Aurora CO 80045, USA. Electronic address: marco.gonzalez@ucdenver.edu.
Heidi L GrabenstatterDepartment of Pediatrics, Division of Neurology, University of Colorado School of Medicine, Aurora, CO, 80045 USA; Translational Epilepsy Research Program, University of Colorado Aurora CO 80045, USA.
Christian A Cea-Del RioDepartment of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA; Translational Epilepsy Research Program, University of Colorado Aurora CO 80045, USA.
Yasmin Cruz Del AngelDepartment of Pediatrics, Division of Neurology, University of Colorado School of Medicine, Aurora, CO, 80045 USA; Translational Epilepsy Research Program, University of Colorado Aurora CO 80045, USA.
Jessica CarlsenDepartment of Pediatrics, Division of Neurology, University of Colorado School of Medicine, Aurora, CO, 80045 USA; Translational Epilepsy Research Program, University of Colorado Aurora CO 80045, USA.
Rick P LaoprasertDepartment of Pediatrics, Division of Neurology, University of Colorado School of Medicine, Aurora, CO, 80045 USA.
Andrew M WhiteDepartment of Pediatrics, Division of Neurology, University of Colorado School of Medicine, Aurora, CO, 80045 USA; Translational Epilepsy Research Program, University of Colorado Aurora CO 80045, USA.
Molly M HuntsmanDepartment of Pediatrics, Division of Neurology, University of Colorado School of Medicine, Aurora, CO, 80045 USA; Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA; Translational Epilepsy Research Program, University of Colorado Aurora CO 80045, USA.
Amy Brooks-KayalDepartment of Pediatrics, Division of Neurology, University of Colorado School of Medicine, Aurora, CO, 80045 USA; Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA; Translational Epilepsy Research Program, University of Colorado Aurora CO 80045, USA; Children's Hospital Colorado, Aurora, CO 80045, USA.

Funding

Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
ZEBRAFISH TRANSGENIC CORE - ROCKY MOUNTAIN NEUROLOGICAL DISORDERS CORE CENTERP30NS048154 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2004 to 2020
$10.1M
GABA(A) Receptor Subunit Regulation in EpileptogenesisR01NS051710 · NINDS · UNIVERSITY OF COLORADO DENVER · PI BROOKS-KAYAL, AMY R., RUSSEK, SHELLEY J · 2006 to 2018
$5.5M
Testing the excitability of inhibitory neuronsR01NS053719 · NINDS · GEORGETOWN UNIVERSITY · PI HUNTSMAN, MOLLY-MAUREEN · 2007 to 2010
$1.1M
GABA(A) RECEPTOR TRAFFICKING AND EPILEPTOGENESISK01NS069583 · NINDS · UNIVERSITY OF COLORADO DENVER · PI GONZALEZ, MARCO I. · 2010 to 2014
$788k
NCATS NIH HHS UL1 TR001082NINDS NIH HHS K01 NS069583NINDS NIH HHS K01-NS069583NINDS NIH HHS P30 NS048154NINDS NIH HHS R01 NS051710NINDS NIH HHS R01-NS051710NINDS NIH HHS R01 NS053719NINDS NIH HHS R01-NS053719
6 · The paper itself

Abstract

In this study, we analyzed the impact that spontaneous seizures might have on the plasma membrane expression, composition and function of GABAA receptors (GABAARs). For this, the tissue of chronically epileptic rats was collected within 3h of seizure occurrence (≤3h group) or at least 24h after seizure occurrence (≥24h group). A retrospective analysis of seizure frequency revealed that selecting animals on the bases of seizure proximity also grouped animals in terms of overall seizure burden with a higher seizure burden observed in the ≤3h group. A biochemical analysis showed that although animals with more frequent/recent seizures (≤3h group) had similar levels of GABAAR at the plasma membrane they showed deficits in inhibitory neurotransmission. By contrast, the tissue obtained from animals experiencing infrequent seizures (≥24h group) had increased plasma membrane levels of GABAAR and showed no deficit in inhibitory function. Together, our findings offer an initial insight into the molecular changes that might help to explain how alterations in GABAAR function can be associated with differential seizure burden. Our findings also suggest that increased plasma membrane levels of GABAAR might act as a compensatory mechanism to more effectively maintain inhibitory function, repress hyperexcitability and reduce seizure burden. This study is an initial step towards a fuller characterization of the molecular events that trigger alterations in GABAergic neurotransmission during chronic epilepsy.

Indexed as

AnimalsBiotinylationDisease Models, AnimalExcitatory Amino Acid AntagonistsGABA AgonistsGene Expression RegulationHippocampusInhibitory Postsynaptic PotentialsIn Vitro TechniquesIsoxazolesMaleMuscarinic AgonistsNeuronsPilocarpineQuinoxalinesRats2-amino-5-phosphopentanoic acidExcitatory Amino Acid AntagonistsFG 9041GABA AgonistsgaboxadolIsoxazolesMuscarinic AgonistsPilocarpineQuinoxalinesReceptors, GABA-AValineEpilepsyEpileptogenesisGABA(A)R regulationSpontaneous seizures

Identifiers

PMID25769812
PMCPMC4415851

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Registered trials

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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.