Evidence map›Paper›PMID 31058213›Full record

ArticleeNeuro

Electroconvulsive Shock Enhances Responsive Motility and Purinergic Currents in Microglia in the Mouse Hippocampus.

Alberto Sepulveda-Rodriguez, Pinggan Li, Tahiyana Khan, James D Ma, Colby A Carlone, P Lorenzo Bozzelli, Katherine E Conant, Patrick A Forcelli, Stefano Vicini

Open access · goldAbstract read
In one paragraph

Article in eNeuro. 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
0.7field-weighted citation impact, top 29% 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, 18 citations in OpenAlex.

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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

9 authors at 2 institutions in 2 countries.

Alberto Sepulveda-RodriguezDepartment of Pharmacology and Physiology, Georgetown University, Washington, DC 20007.ORCID 0000-0002-6479-8635
Pinggan LiDepartment of Pharmacology and Physiology, Georgetown University, Washington, DC 20007.
Tahiyana KhanDepartment of Pharmacology and Physiology, Georgetown University, Washington, DC 20007.
James D MaDepartment of Pharmacology and Physiology, Georgetown University, Washington, DC 20007.
Colby A CarloneDepartment of Pharmacology and Physiology, Georgetown University, Washington, DC 20007.
P Lorenzo BozzelliInterdisciplinary Program in Neuroscience, Georgetown University, Washington, DC 20007.
Katherine E ConantInterdisciplinary Program in Neuroscience, Georgetown University, Washington, DC 20007.
Patrick A ForcelliDepartment of Pharmacology and Physiology, Georgetown University, Washington, DC 20007.
Stefano ViciniDepartment of Pharmacology and Physiology, Georgetown University, Washington, DC 20007.ORCID 0000-0001-8671-5194
Georgetown University · USSun Yat-sen University · CN

Funding

Institutional Career Development CoreKL2TR001432 · NCATS · GEORGETOWN UNIVERSITY · PI UMANS, JASON G · 2015 to 2024
$7.5M
Training in Neural Injury &PlasticityT32NS041218 · NINDS · GEORGETOWN UNIVERSITY · PI MARK P BURNS, Kathleen Anne Maguire-Zeiss · 2001 to 2026
$3.5M
Structural and functional sequelae of neonatal anticonvulsant exposure: drug-seizure interactionsR01HD091994 · NICHD · GEORGETOWN UNIVERSITY · PI FORCELLI, PATRICK ALEXANDER · 2018 to 2022
$2.9M
NCATS NIH HHS KL2 TR001432NICHD NIH HHS R01 HD091994NINDS NIH HHS T32 NS041218
6 · The paper itself

Abstract

Microglia are in a privileged position to both affect and be affected by neuroinflammation, neuronal activity and injury, which are all hallmarks of seizures and the epilepsies. Hippocampal microglia become activated after prolonged, damaging seizures known as status epilepticus (SE). However, since SE causes both hyperactivity and injury of neurons, the mechanisms triggering this activation remain unclear, as does the relevance of the microglial activation to the ensuing epileptogenic processes. In this study, we use electroconvulsive shock (ECS) to study the effect of neuronal hyperactivity without neuronal degeneration on mouse hippocampal microglia. Unlike SE, ECS did not alter hippocampal CA1 microglial density, morphology, or baseline motility. In contrast, both ECS and SE produced a similar increase in ATP-directed microglial process motility in acute slices, and similarly upregulated expression of the chemokine C-C motif chemokine ligand 2 (CCL2). Whole-cell patch-clamp recordings of hippocampal CA1

Indexed as

CA1 Region, HippocampalElectroshockInflammationStatus EpilepticusAdenosine TriphosphateAnimalsCell MovementDisease Models, AnimalElectrophysiological PhenomenaFemaleMaleMiceMicrogliaPatch-Clamp TechniquesReceptors, Purinergic P2X7Up-RegulationAdenosine TriphosphateReceptors, Purinergic P2X7ATPECTepilepsyneuroinflammationpatch-clamp electrophysiologyseizures

Identifiers

PMID31058213
PMCPMC6498419
OpenAlexW2938457224

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.