Evidence map›Paper›PMID 36120099›Full record

ArticleFrontiers in neuroanatomy2022

Neural activity patterns in the chemosensory network encoding vomeronasal and olfactory information in mice.

Cecília Pardo-Bellver, Manuel E Vila-Martin, Sergio Martínez-Bellver, María Villafranca-Faus, Anna Teruel-Sanchis, Camila A Savarelli-Balsamo, Sylwia M Drabik, Joana Martínez-Ricós, Ana Cervera-Ferri, Fernando Martínez-García and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroanatomy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. The olfactory limbus of the red fox (Frontiers in neuroanatomy · 2022
    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

12 authors at 3 institutions in 2 countries.

Cecília Pardo-BellverDepartment of Functional and Cell Biology, Faculty of Biology, University of Valencia, Valencia, Spain.
Manuel E Vila-MartinDepartment of Functional and Cell Biology, Faculty of Biology, University of Valencia, Valencia, Spain.
Sergio Martínez-BellverLaboratory of Neuronal Circuits, Department of Human Anatomy and Embryology, Faculty of Medicine, University of Valencia, Valencia, Spain.
María Villafranca-FausLaboratory of Neuronal Circuits, Department of Human Anatomy and Embryology, Faculty of Medicine, University of Valencia, Valencia, Spain.
Anna Teruel-SanchisDepartment of Functional and Cell Biology, Faculty of Biology, University of Valencia, Valencia, Spain.
Camila A Savarelli-BalsamoDepartment of Functional and Cell Biology, Faculty of Biology, University of Valencia, Valencia, Spain.
Sylwia M DrabikDepartment of Functional and Cell Biology, Faculty of Biology, University of Valencia, Valencia, Spain.
Joana Martínez-RicósLaboratory of Neuronal Circuits, Department of Human Anatomy and Embryology, Faculty of Medicine, University of Valencia, Valencia, Spain.
Ana Cervera-FerriLaboratory of Neuronal Circuits, Department of Human Anatomy and Embryology, Faculty of Medicine, University of Valencia, Valencia, Spain.
Fernando Martínez-GarcíaFaculty of Health Sciences, Pre-Departmental Unit of Medicine, Jaume I University, Castellón de la Plana, Spain.
Enrique LanuzaDepartment of Functional and Cell Biology, Faculty of Biology, University of Valencia, Valencia, Spain.
Vicent Teruel-MartíLaboratory of Neuronal Circuits, Department of Human Anatomy and Embryology, Faculty of Medicine, University of Valencia, Valencia, Spain.
Universitat de València · ESJagiellonian University · PLUniversitat Jaume I · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rodents detect chemical information mainly through the olfactory and vomeronasal systems, which play complementary roles to orchestrate appropriate behavioral responses. To characterize the integration of chemosensory information, we have performed electrophysiological and c-Fos studies of the bulbo-amygdalar network in freely behaving female mice exploring neutral or conspecific stimuli. We hypothesize that processing conspecifics stimuli requires both chemosensory systems, and thus our results will show shared patterns of activity in olfactory and vomeronasal structures. Were the hypothesis not true, the activity of the vomeronasal structures would be independent of that of the main olfactory system. In the c-Fos analysis, we assessed the activation elicited by neutral olfactory or male stimuli in a broader network. Male urine induced a significantly higher activity in the vomeronasal system compared to that induced by a neutral odorant. Concerning the olfactory system, only the cortex-amygdala transition area showed significant activation. No differential c-Fos expression was found in the reward system and the basolateral amygdala. These functional patterns in the chemosensory circuitry reveal a strong top-down control of the amygdala over both olfactory bulbs, suggesting an active role of the amygdala in the integration of chemosensory information directing the activity of the bulbs during environmental exploration.

Indexed as

accessory olfactory systemamygdalac-FosGranger causalityoscillations

Identifiers

PMID36120099
PMCPMC9479637
OpenAlexW4294287431

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.