Evidence map›Paper›PMID 19846720›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2009

In vivo role of a potassium channel-binding protein in regulating neuronal excitability and behavior.

Mohammad Shahidullah, Smitha Reddy, Hong Fei, Irwin B Levitan

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 33% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Evidence thatbioRxiv : the preprint server for biology · 2025
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  6. Review
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  8. Cell-specific fine-tuning of neuronal excitability by differential expression of modulator protein isoforms.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
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  13. A novel auxiliary subunit critical to BK channel function in Caenorhabditis elegans.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2010
    Article
  14. Article
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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

4 authors at 2 institutions in 1 country.

Mohammad ShahidullahDepartment of Neuroscience, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
Smitha Reddy
Hong Fei
Irwin B Levitan
University of Pennsylvania · USFox Chase Cancer Center · US

Funding

REGULATION OF ION CHANNELS IN NERVE CELLSR01NS017910 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI LEVITAN, IRWIN B · 1985 to 2009
$3.9M
NINDS NIH HHS R01 NS017910
6 · The paper itself

Abstract

Molecular details of ion channel interactions with modulatory subunits have been investigated widely in transfected cells, but the physiological roles of ion channel modulatory protein complexes in native neurons remain largely unexplored. The Drosophila large-conductance calcium-activated potassium channel (dSlo) binds to and is modulated by its binding partner Slob. We have constructed flies in which Slob expression is manipulated by P-element mutagenesis, or by transgenic expression of Slob protein or Slob-RNAi. In vivo recordings of both macroscopic and single dSlo channel currents in identified neurosecretory neurons in the pars intercerebralis (PI) region of the Drosophila brain reveal that whole-cell potassium current and properties of single dSlo channels are modulated by Slob expression level. Furthermore, Slob genotype influences action potential duration in vivo. This unprecedented combination of current-clamp, macroscopic-current, and single-channel recordings from neurons in brains of living flies defines a critical role for an ion channel modulatory protein complex in the control of neuronal excitability. We show further that Slob-null flies exhibit significantly longer lifespan than controls under conditions of complete food deprivation. Crosses with deficiency lines demonstrate that this enhanced resistance to starvation-induced death maps close to the slob locus. Together, these results indicate that Slob may serve a novel regulatory function in feeding behavior, possibly by influencing the excitability of the PI neurons.

Indexed as

AnimalsAnimals, Genetically ModifiedBehavior, AnimalBiophysical PhenomenaCerebellumDrosophilaDrosophila ProteinsElectric ConductivityElectric StimulationFeeding BehaviorFood DeprivationGene Expression RegulationGreen Fluorescent ProteinsIon Channel GatingMembrane PotentialsMutagenesisDrosophila ProteinsGreen Fluorescent ProteinsPotassium Channel BlockersPotassium ChannelsRNA, Small InterferingSlob protein, DrosophilaTetraethylammonium

Identifiers

PMID19846720
PMCPMC2785714
OpenAlexW1986741414

What OpenQuestion holds

Textmetadata
LicenceTDM
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.