Evidence map›Paper›PMID 26587966›Full record

ArticleThe Journal of comparative neurology2016

Differential distribution of the sodium-activated potassium channels slick and slack in mouse brain.

Sandra Rizzi, Hans-Günther Knaus, Christoph Schwarzer

Open access · hybridAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 82 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Andrology · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. Heterozygous expression of abioRxiv : the preprint server for biology · 2024
    Article
  10. Article
  11. Article
  12. Increased Expression of KNeurochemical research · 2024
    Article
  13. Article
  14. Identification of a novelFrontiers in genetics · 2024
    Article
  15. Slack KCommunications biology · 2023
    Article
  16. Distinct Features of Interictal Activity Predict Seizure Localization and Burden in a Mouse Model of Childhood Epilepsy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  17. Review
  18. Reduction ofFrontiers in neuroscience · 2023
    Article
  19. Single Nuclei Analyses Reveal Transcriptional Profiles and Marker Genes for Diverse Supraspinal Populations.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  20. KNeurobiology of disease · 2022
    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

3 authors at 2 institutions in 1 country.

Sandra RizziDivision of Molecular and Cellular Pharmacology, Medical University of Innsbruck, 6020, Innsbruck, Austria.
Hans-Günther KnausDivision of Molecular and Cellular Pharmacology, Medical University of Innsbruck, 6020, Innsbruck, Austria.
Christoph SchwarzerDepartment of Pharmacology, Medical University of Innsbruck, 6020, Innsbruck, Austria.
Innsbruck Medical University · ATUniversität Innsbruck · AT

Funding

Austrian Science Fund FWF W 1206
6 · The paper itself

Abstract

The sodium-activated potassium channels Slick (Slo2.1, KCNT2) and Slack (Slo2.2, KCNT1) are high-conductance potassium channels of the Slo family. In neurons, Slick and Slack channels are involved in the generation of slow afterhyperpolarization, in the regulation of firing patterns, and in setting and stabilizing the resting membrane potential. The distribution and subcellular localization of Slick and Slack channels in the mouse brain have not yet been established in detail. The present study addresses this issue through in situ hybridization and immunohistochemistry. Both channels were widely distributed and exhibited distinct distribution patterns. However, in some brain regions, their expression overlapped. Intense Slick channel immunoreactivity was observed in processes, varicosities, and neuronal cell bodies of the olfactory bulb, granular zones of cortical regions, hippocampus, amygdala, lateral septal nuclei, certain hypothalamic and midbrain nuclei, and several regions of the brainstem. The Slack channel showed primarily a diffuse immunostaining pattern, and labeling of cell somata and processes was observed only occasionally. The highest Slack channel expression was detected in the olfactory bulb, lateral septal nuclei, basal ganglia, and distinct areas of the midbrain, brainstem, and cerebellar cortex. In addition, comparing our data obtained from mouse brain with a previously published study on rat brain revealed some differences in the expression and distribution of Slick and Slack channels in these species. J. Comp. Neurol. 524:2093-2116, 2016. © 2015 The Authors The Journal of Comparative Neurology Published by Wiley Periodicals, Inc.

Indexed as

AnimalsBrainCell MembraneHEK293 CellsHumansMiceMice, Inbred C57BLNerve Tissue ProteinsPotassium ChannelsPotassium Channels, Sodium-ActivatedRNA, MessengerTransfectionKcnt2 protein, mouseNerve Tissue ProteinsPotassium ChannelsPotassium Channels, Sodium-ActivatedRNA, MessengerSlo2 protein, mousedistributionexpressionKCNT1KCNT2mouse brainSlo2 channels

Identifiers

PMID26587966
PMCPMC4982087
OpenAlexW2178543746

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.