Evidence map›Paper›PMID 27009162›Full record

ArticleJournal of neurophysiology2016

Biophysical constraints on lateral inhibition in the olfactory bulb.

Alexa B R McIntyre, Thomas A Cleland

Open access · greenAbstract 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Connectivity and dynamics in the olfactory bulb.PLoS computational biology · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Noradrenergic Activity in the Olfactory Bulb Is a Key Element for the Stability of Olfactory Memory.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  10. Article
  11. Article
  12. A Systematic Framework for Olfactory Bulb Signal Transformations.Frontiers in computational neuroscience · 2020
    Article
  13. Article
  14. Spatial Structure of Synchronized Inhibition in the Olfactory Bulb.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  15. Review
  16. 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

2 authors at 1 institution in 1 country.

Alexa B R McIntyreTri-Institutional Program in Computational Biology and Medicine, Cornell University, Ithaca, New York; and.
Thomas A ClelandDepartment of Psychology, Cornell University, Ithaca, New York tac29@cornell.edu.ORCID 0000-0001-7506-1201
Cornell University · US

Funding

Circuit architecture and dynamics representation in odor perceptionR01DC014701 · NIDCD · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI Thomas A Cleland, Yingxi Lin · 2015 to 2026
$6.4M
CRCNS: Dynamical mechanisms of oscillation transitions in the olfactory systemR01DC014367 · NIDCD · UNIVERSITY OF CHICAGO · PI CLELAND, THOMAS A, KAY, LESLIE M · 2014 to 2018
$1.6M
NIDCD NIH HHS R01 DC014367NIDCD NIH HHS R01 DC014701
6 · The paper itself

Abstract

The mitral cells (MCs) of the mammalian olfactory bulb (OB) constitute one of two populations of principal neurons (along with middle/deep tufted cells) that integrate afferent olfactory information with top-down inputs and intrinsic learning and deliver output to downstream olfactory areas. MC activity is regulated in part by inhibition from granule cells, which form reciprocal synapses with MCs along the extents of their lateral dendrites. However, with MC lateral dendrites reaching over 1.5 mm in length in rats, the roles of distal inhibitory synapses pose a quandary. Here, we systematically vary the properties of a MC model to assess the capacity of inhibitory synaptic inputs on lateral dendrites to influence afferent information flow through MCs. Simulations using passivized models with varying dendritic morphologies and synaptic properties demonstrated that, even with unrealistically favorable parameters, passive propagation fails to convey effective inhibitory signals to the soma from distal sources. Additional simulations using an active model exhibiting action potentials, subthreshold oscillations, and a dendritic morphology closely matched to experimental values further confirmed that distal synaptic inputs along the lateral dendrite could not exert physiologically relevant effects on MC spike timing at the soma. Larger synaptic conductances representative of multiple simultaneous inputs were not sufficient to compensate for the decline in signal with distance. Reciprocal synapses on distal MC lateral dendrites may instead serve to maintain a common fast oscillatory clock across the OB by delaying spike propagation within the lateral dendrites themselves.

Indexed as

AnimalsCell ShapeCell SizeComputer SimulationElectric ImpedanceMembrane PotentialsModels, NeurologicalNeural InhibitionNeuronsOlfactory BulbReceptors, GABA-ASmellSynapsesReceptors, GABA-Acable theorycomputational neurosciencelateral dendritesmitral cellolfaction

Identifiers

PMID27009162
PMCPMC4922614
OpenAlexW2303469401

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.