Evidence map›Paper›PMID 27075543›Full record

ArticleJournal of neurophysiology2016

A sodium afterdepolarization in rat superior colliculus neurons and its contribution to population activity.

Nima Ghitani, Peter O Bayguinov, Michele A Basso, Meyer B Jackson

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Intrinsic and Synaptic Contributions to Repetitive Spiking in Dentate Granule Cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  3. Oxaliplatin Depolarizes the IB4Frontiers in molecular neuroscience · 2021
    Article
  4. Article
  5. Review
  6. Neuronal hyperexcitability in a mouse model ofProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  7. Article
  8. 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

4 authors.

Nima GhitaniDepartment of Neuroscience and Neuroscience Training Program, The University of Wisconsin, Madison, Wisconsin; and.
Peter O BayguinovDepartment of Neuroscience and Neuroscience Training Program, The University of Wisconsin, Madison, Wisconsin; and.
Michele A BassoDepartment of Psychiatry and Biobehavioral Sciences and Department of Neurobiology, The Fuster Laboratory for Cognitive Neuroscience, The Semel Institute for Neuroscience and Human Behavior, and The Brain Research Institute, The David Geffen School of Medicine, University of California, Los Angeles, California.
Meyer B JacksonDepartment of Neuroscience and Neuroscience Training Program, The University of Wisconsin, Madison, Wisconsin; and meyer.jackson@wisc.edu.

Funding

NEUROSCIENCE TRAINING PROGRAMT32GM007507 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI HALLORAN, MARY C · 1985 to 2017
$9.3M
An in vitro model of saccadic eye movement choiceR01EY019663 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI BASSO, MICHELE A · 2010 to 2019
$3.5M
A new model of the role of the basal ganglia in eye movement initiation.R21EY024153 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BASSO, MICHELE A, HALL, WILLIAM CHARLES · 2014 to 2015
$392k
NEI NIH HHS R01 EY019663NEI NIH HHS R21 EY024153NIGMS NIH HHS T32 GM007507
6 · The paper itself

Abstract

The mammalian superior colliculus (SC) is a midbrain structure that integrates multimodal sensory inputs and computes commands to initiate rapid eye movements. SC neurons burst with the sudden onset of a visual stimulus, followed by persistent activity that may underlie shifts of attention and decision making. Experiments in vitro suggest that circuit reverberations play a role in the burst activity in the SC, but the origin of persistent activity is unclear. In the present study we characterized an afterdepolarization (ADP) that follows action potentials in slices of rat SC. Population responses seen with voltage-sensitive dye imaging consisted of rapid spikes followed immediately by a second distinct depolarization of lower amplitude and longer duration. Patch-clamp recordings showed qualitatively similar behavior: in nearly all neurons throughout the SC, rapid spikes were followed by an ADP. Ionic and pharmacological manipulations along with experiments with current and voltage steps indicated that the ADP of SC neurons arises from Na(+) current that either persists or resurges following Na(+) channel inactivation at the end of an action potential. Comparisons of pharmacological properties and frequency dependence revealed a clear parallel between patch-clamp recordings and voltage imaging experiments, indicating a common underlying membrane mechanism for the ADP in both single neurons and populations. The ADP can initiate repetitive spiking at intervals consistent with the frequency of persistent activity in the SC. These results indicate that SC neurons have intrinsic membrane properties that can contribute to electrical activity that underlies shifts of attention and decision making.

Indexed as

AnimalsMembrane PotentialsNeuronsPatch-Clamp TechniquesRats, Sprague-DawleySodiumSodium Channel BlockersSodium ChannelsSuperior ColliculiTissue Culture TechniquesVoltage-Sensitive Dye ImagingSodiumSodium Channel BlockersSodium Channelseye movementsNa+ channelspersistent activity

Identifiers

PMID27075543
PMCPMC4961755

What OpenQuestion holds

Textmetadata
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.