Evidence map›Paper›PMID 27110919›Full record

ArticleNature neuroscience2016

Serotonin modulates spike probability in the axon initial segment through HCN channels.

Kwang Woo Ko, Matthew N Rasband, Victor Meseguer, Richard H Kramer, Nace L Golding

Abstract read
In one paragraph

Article in Nature neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

59 citing papers in PubMed, 97 citations in OpenAlex.

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  18. Arrestin-3 Agonism at Dopamine DBiological psychiatry · 2023
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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

5 authors at 3 institutions in 1 country.

Kwang Woo KoDepartment of Neuroscience, University of Texas at Austin, Austin, Texas, USA.
Matthew N RasbandDepartment of Neuroscience, Baylor College of Medicine, Houston, Texas, USA.
Victor MeseguerDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, California, USA.
Richard H KramerDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, California, USA.
Nace L GoldingDepartment of Neuroscience, University of Texas at Austin, Austin, Texas, USA.
The University of Texas at Austin · USUniversity of California, Berkeley · USBaylor College of Medicine · US

Funding

Dendritic Integration and Synaptic Plasticity in the MSOR01DC006877 · NIDCD · UNIVERSITY OF TEXAS AUSTIN · PI GOLDING, NACE L · 2004 to 2022
$5.9M
Understanding how photoswitches restore visual function in blindnessR01EY024334 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI KRAMER, RICHARD H · 2015 to 2024
$4.4M
Neuroglial Interactions at the Node of RanvierR01NS044916 · NINDS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI RASBAND, MATTHEW N · 2002 to 2020
$4.2M
Neuroglial interactions at the node of RanvierR37NS044916 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI RASBAND, MATTHEW N · 2012 to 2018
$2.9M
Light-activated ion chanenls for remote control of neuronal activityR01EY018957 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI KRAMER, RICHARD H · 2008 to 2011
$1.6M
Neurocognition of Auditory Word ProcessingF32DC006788 · NIDCD · UNIVERSITY OF MARYLAND COLLEGE PK CAMPUS · PI BOWLES, ANITA R · 2004 to 2005
$60k
NEI NIH HHS R01 EY018957NEI NIH HHS R01 EY024334NIDCD NIH HHS F32 DC006788NIDCD NIH HHS R01 DC006877NINDS NIH HHS R01 NS044916NINDS NIH HHS R37 NS044916
6 · The paper itself

Abstract

The axon initial segment (AIS) serves as the site of action potential initiation in most neurons, but difficulties in isolating the effects of voltage-gated ion channels in the AIS from those of the soma and dendrites have hampered understanding how AIS properties influence neural coding. Here we have combined confocal microscopy, patch-clamp recordings and light-sensitive channel blockers ('photoswitches') in binaural auditory gerbil neurons to show that hyperpolarization and cyclic-nucleotide-gated (HCN) channels are expressed in the AIS and decrease spike probability, in a manner distinct from that of HCN channels in the soma and dendrites. Furthermore, the control of spike threshold by HCN channels in the AIS can be altered through serotonergic modulation of 5-hydroxytryptamine 1A (5-HT1A) receptors, which hyperpolarizes the activation range of HCN channels. As release of serotonin signals changes in motivation and attention states, axonal HCN channels provide a mechanism to translate these signals into changes in the threshold for sensory stimuli.

Indexed as

Action PotentialsAnimalsAxon Initial SegmentAxonsCyclic Nucleotide-Gated Cation ChannelsDendritesGerbillinaeHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsPatch-Clamp TechniquesSerotoninCyclic Nucleotide-Gated Cation ChannelsHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsSerotonin

Identifiers

PMID27110919
PMCPMC4882252
OpenAlexW2342656908

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.