Evidence map›Paper›PMID 27490056›Full record

ArticleThe Journal of comparative neurology2017

Three-dimensional synaptic analyses of mitral cell and external tufted cell dendrites in rat olfactory bulb glomeruli.

Jennifer N Bourne, Nathan E Schoppa

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Serotonergic Modulation of Olfaction in Rodents and Insects.The Yale journal of biology and medicine · 2018
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. 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.

Jennifer N BourneDepartment of Physiology and Biophysics, University of Colorado School of Medicine, Aurora, Colorado, 80045.
Nathan E SchoppaDepartment of Physiology and Biophysics, University of Colorado School of Medicine, Aurora, Colorado, 80045.
University of Colorado Denver · US

Funding

PERIPHERAL MECHANISMS OF OLFACTORY RECEPTIONR01DC000566 · NIDCD · UNIVERSITY OF COLORADO DENVER · PI RESTREPO, DIEGO · 1989 to 2022
$9.9M
Mechanisms of olfactory signal processingR01DC006640 · NIDCD · UNIVERSITY OF COLORADO DENVER · PI SCHOPPA, NATHAN ERIC · 2005 to 2025
$6.8M
NIDCD NIH HHS R01 DC000566NIDCD NIH HHS R01 DC006640
6 · The paper itself

Abstract

Recent studies have suggested that the two excitatory cell classes of the mammalian olfactory bulb, the mitral cells (MCs) and tufted cells (TCs), differ markedly in physiological responses. For example, TCs are more sensitive and broadly tuned to odors than MCs and also are much more sensitive to stimulation of olfactory sensory neurons (OSNs) in bulb slices. To examine the morphological bases for these differences, we performed quantitative ultrastructural analyses of glomeruli in rat olfactory bulb under conditions in which specific cells were labeled with biocytin and 3,3'-diaminobenzidine. Comparisons were made between MCs and external TCs (eTCs), which are a TC subtype in the glomerular layer with large, direct OSN signals and capable of mediating feedforward excitation of MCs. Three-dimensional analysis of labeled apical dendrites under an electron microscope revealed that MCs and eTCs in fact have similar densities of several chemical synapse types, including OSN inputs. OSN synapses also were distributed similarly, favoring a distal localization on both cells. Analysis of unlabeled putative MC dendrites further revealed gap junctions distributed uniformly along the apical dendrite and, on average, proximally with respect to OSN synapses. Our results suggest that the greater sensitivity of eTCs vs. MCs is due not to OSN synapse number or absolute location but rather to a conductance in the MC dendrite that is well positioned to attenuate excitatory signals passing to the cell soma. Functionally, such a mechanism could allow rapid and dynamic control of OSN-driven action potential firing in MCs through changes in gap junction properties. J. Comp. Neurol. 525:592-609, 2017. © 2016 Wiley Periodicals, Inc.

Indexed as

3,3'-DiaminobenzidineAnimalsDendritesFemaleGap JunctionsImaging, Three-DimensionalLysineMaleMicroscopy, ElectronMicroscopy, FluorescenceNeural InhibitionOlfactory BulbPatch-Clamp TechniquesRats, Sprague-DawleySynapses3,3'-DiaminobenzidinebiocytinLysinegap junctionsglomerulusolfactionreconstructionsRRID:SCR_002716sensory neuronserial section electron microscopy

Identifiers

PMID27490056
PMCPMC5648330
OpenAlexW2487348324

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.