Evidence map›Paper›PMID 31783064›Full record

ArticleNeuropharmacology2020

Activation of small conductance calcium-activated potassium channels suppresses seizure susceptibility in the genetically epilepsy-prone rats.

Padmini Khandai, Patrick A Forcelli, Prosper N'Gouemo

Abstract read
In one paragraph

Article in Neuropharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Small-Conductance CaNeuroscience bulletin · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Calcium-Activated Potassium Channel KMolecular neurobiology · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Review
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

3 authors.

Padmini KhandaiDepartments of Pediatrics, Georgetown University Medical Center, Washington, USA.
Patrick A ForcelliDepartment of Pharmacology and Physiology, Georgetown University Medical Center, Washington DC, USA; Department of Neuroscience, Georgetown University Medical Center, Washington DC, USA; Interdisciplinary Program in Neuroscience, Georgetown University Medical Center, Washington DC, USA.
Prosper N'GouemoDepartments of Pediatrics, Georgetown University Medical Center, Washington, USA; Department of Pharmacology and Physiology, Georgetown University Medical Center, Washington DC, USA; Interdisciplinary Program in Neuroscience, Georgetown University Medical Center, Washington DC, USA. Electronic address: pn@georgetown.edu.

Funding

Research_ProjectU54HD090257 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI VITTORIO GALLO, VITTORIO GALLO VITTORIO GALLO · 2016 to 2020
$5.9M
Optogenetic control of seizures via the basal gangliaR01NS097762 · NINDS · GEORGETOWN UNIVERSITY · PI Patrick Alexander Forcelli · 2016 to 2026
$4.1M
Mechanisms of Alcohol Withdrawal Seizures: Role of L-type Ca2+ ChannelsR01AA020073 · NIAAA · GEORGETOWN UNIVERSITY · PI N'GOUEMO, PROSPER · 2011 to 2015
$1.7M
Pediatric seizures: role of IP3R Ca2+ release channelsR21AA027171 · NIAAA · HOWARD UNIVERSITY · PI N'GOUEMO, PROSPER · 2018 to 2019
$408k
NIAAA NIH HHS R01 AA020073NIAAA NIH HHS R21 AA027171NICHD NIH HHS U54 HD090257NINDS NIH HHS R01 NS097762
6 · The paper itself

Abstract

Small conductance calcium-activated potassium (SK) channels dampen neuronal excitability by contributing to slow afterhyperpolarization (AHP) that follows a series of action potentials, and therefore may represent an intrinsic inhibitory mechanism to prevent seizures. We have previously reported that susceptibility to acoustically evoked seizures was associated with downregulation of SK1 and SK3 subtypes of SK channels in the inferior colliculus of the moderated seizure severity strain of the genetically epilepsy-prone rats (GEPR-3s). Here, we evaluated the effects of 1-ethyl-2-benzimidazolinone (1-EBIO), a potent activator of SK channels, on acoustically evoked seizures in both male and female adult GEPR-3s at various time points post-treatment. Systemic administration of 1-EBIO at various tested doses suppressed seizure susceptibility in both male and female GEPR-3s; however, the complete seizure suppression was only observed following administration of relatively higher doses of 1-EBIO in females. These findings indicate that activation of SK channels results in anticonvulsive action against generalized tonic-clonic seizures in both male and female GEPR-3s, with males exhibiting higher sensitivity than females.

Indexed as

Action PotentialsAnimalsBenzimidazolesEpilepsyFemaleMaleRatsSeizuresSmall-Conductance Calcium-Activated Potassium Channels1-ethyl-2-benzimidazolinoneBenzimidazolesSmall-Conductance Calcium-Activated Potassium Channels6): 1-ethyl-2-benzimidazoline (1-EBIO)Audiogenic seizuresCalcium-activated potassium channelHyperexcitabilityInherited epilepsy

Identifiers

PMID31783064
PMCPMC6939461

What OpenQuestion holds

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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.