Evidence map›Paper›PMID 19198607›Full record

ArticleNature neuroscience2009

Spike frequency adaptation mediates looming stimulus selectivity in a collision-detecting neuron.

Simon Peron, Fabrizio Gabbiani

Abstract readComparative Study
In one paragraph

Article in Nature neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing 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

68 citing papers in PubMed.

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  10. Tonotopic CaJournal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2024
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8 more citing papers are in PubMed but not listed here.

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

2 authors.

Simon PeronDepartment of Neuroscience, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.
Fabrizio Gabbiani

Funding

Neuronal Mechanisms of Multiplication and InvarianceR01MH065339 · NIMH · BAYLOR COLLEGE OF MEDICINE · PI GABBIANI, FABRIZIO · 2002 to 2017
$4.5M
NIMH NIH HHS R01 MH065339
6 · The paper itself

Abstract

How active membrane conductance dynamics tunes neurons for specific time-varying stimuli remains poorly understood. We studied the biophysical mechanisms by which spike frequency adaptation shapes visual stimulus selectivity in an identified visual interneuron of the locust. The lobula giant movement detector (LGMD) responds preferentially to objects approaching on a collision course with the locust. Using calcium imaging, pharmacology and modeling, we show that spike frequency adaptation in the LGMD is mediated by a Ca(2+)-dependent potassium conductance closely resembling those associated with 'small-conductance' (SK) channels. Intracellular block of this conductance minimally affected the LGMD's response to approaching stimuli, but substantially increased its response to translating ones. Thus, spike frequency adaptation contributes to the neuron's tuning by selectively decreasing its responses to nonpreferred stimuli. Our results identify a new mechanism by which spike frequency adaptation may tune visual neurons to behaviorally relevant stimuli.

Indexed as

Action PotentialsAdaptation, PhysiologicalAnimalsFemaleGrasshoppersMotion PerceptionNeuronsPhotic StimulationTime Factors

Identifiers

PMID19198607
PMCPMC2662764

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.