Evidence map›Paper›PMID 29066953›Full record

ArticleFrontiers in cellular neuroscience2017

Disturbances in the FGFR1-5-HT1A Heteroreceptor Complexes in the Raphe-Hippocampal 5-HT System Develop in a Genetic Rat Model of Depression.

Dasiel O Borroto-Escuela, Caitlin M DuPont, Xiang Li, David Savelli, Davide Lattanzi, Ipsit Srivastava, Manuel Narváez, Michael Di Palma, Elisa Barbieri, Yuniesky Andrade-Talavera and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

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  14. The Role of Serotonin in Singultus: A Review.Frontiers in neuroscience · 2020
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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

16 authors at 5 institutions in 6 countries.

Dasiel O Borroto-EscuelaDivision of Cellular and Molecular Neurochemistry, Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Caitlin M DuPontDivision of Cellular and Molecular Neurochemistry, Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Xiang LiDivision of Cellular and Molecular Neurochemistry, Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
David SavelliDivision of Cellular and Molecular Neurochemistry, Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Davide LattanziDepartment of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Ipsit SrivastavaDivision of Cellular and Molecular Neurochemistry, Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Manuel NarváezInstituto de Investigación Biomédica de Málaga, Facultad de Medicina, Universidad de Málaga, Málaga, Spain.
Michael Di PalmaDepartment of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Elisa BarbieriDivision of Cellular and Molecular Neurochemistry, Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Yuniesky Andrade-TalaveraNeuronal Oscillations Laboratory, Department of Neurobiology, Care Sciences and Society, Center for Alzheimer Research, Karolinska Institutet, Stockholm, Sweden.
Riccardo CuppiniDepartment of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Yuji OdagakiDepartment of Psychiatry, Faculty of Medicine, Saitama Medical University, Saitama, Japan.
Miklos PalkovitsDepartment of Anatomy, Histology and Embryology, Semmelweis University, Budapest, Hungary.
Patrizia AmbroginiDepartment of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Maria LindskogDivision of Cellular and Molecular Neurochemistry, Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Kjell FuxeDivision of Cellular and Molecular Neurochemistry, Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Karolinska Institutet · SEUniversity of Urbino · ITSaitama Medical University · JPSemmelweis University · HUUniversidad de Málaga · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The FGFR1-5-HT1A heteroreceptor complexes are involved in neuroplasticity in the rat hippocampus and in the mesencephalic raphe 5-HT nerve cells. There exists a 5-HT1A protomer enhancement of FGFR1 protomer signaling. Acute and 10 day treatment with intracerebroventricular (i.c.v.) FGF-2 and the 5-HT1A agonist 8-OH-DPAT produced enhanced antidepressant effects in the forced swim test (FST). We studied in the current work the disturbances in the FGFR1-5-HT1A heterocomplexes in a genetic rat model of depression, the Flinders sensitive line (FSL) rats of Sprague-Dawley (SD) origin, by means of neurochemical, neurophysiological and behavioral techniques. In control SD rats, the FGFR1 agonist SUN11602 and FGF2 produced a significant reduction of G protein-coupled inwardly rectifying K

Indexed as

5-HT1A receptordepressiondimerizationfibroblast growth factor receptor 1heteroreceptor complexeshippocampusraphereceptor-receptor interaction

Identifiers

PMID29066953
PMCPMC5641403
OpenAlexW2760965380

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.