Evidence map›Paper›PMID 32464686›Full record

ArticleBritish journal of pharmacology2020

6-Hydroxydopamine lesion and levodopa treatment modify the effect of buspirone in the substantia nigra pars reticulata.

Sergio Vegas-Suárez, Clarissa Anna Pisanò, Catalina Requejo, Harkaitz Bengoetxea, Jose Vicente Lafuente, Michele Morari, Cristina Miguelez, Luisa Ugedo

Open access · hybridAbstract read
In one paragraph

Article in British journal of pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  7. The effect of 5-HTBritish journal of pharmacology · 2021
    Article
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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

8 authors at 2 institutions in 2 countries.

Sergio Vegas-SuárezDepartment of Pharmacology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), Leioa, Spain.ORCID 0000-0001-5925-189X
Clarissa Anna PisanòDepartment of Medical Sciences, Section of Pharmacology, University of Ferrara, Ferrara, Italy.ORCID 0000-0001-9659-7400
Catalina RequejoLaNCE, Department of Neuroscience, University of the Basque Country (UPV/EHU), Leioa, Spain.ORCID 0000-0002-5440-5455
Harkaitz BengoetxeaLaNCE, Department of Neuroscience, University of the Basque Country (UPV/EHU), Leioa, Spain.ORCID 0000-0002-7805-2420
Jose Vicente LafuenteLaNCE, Department of Neuroscience, University of the Basque Country (UPV/EHU), Leioa, Spain.ORCID 0000-0001-7246-0987
Michele MorariDepartment of Medical Sciences, Section of Pharmacology, University of Ferrara, Ferrara, Italy.ORCID 0000-0002-4601-4454
Cristina MiguelezDepartment of Pharmacology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), Leioa, Spain.ORCID 0000-0001-6624-2932
Luisa UgedoDepartment of Pharmacology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), Leioa, Spain.ORCID 0000-0001-5993-0606
University of the Basque Country · ESUniversity of Ferrara · IT

Funding

Eusko Jaurlaritza IT747-13Eusko Jaurlaritza T747-13Ministerio de Economía y Competitividad SAF2016-77758-R
6 · The paper itself

Abstract

background and purposel-DOPA-induced dyskinesia (LID) is considered a major complication in the treatment of Parkinson's disease (PD). Buspirone (5-HT EXPERIMENTAL APPROACH: Buspirone was studied using in vivo single-unit, electrocorticogram, local field potential recordings along with microdialysis and immunohistochemistry in naïve/sham, 6-hydroxydopamine (6-OHDA)-lesioned or 6-OHDA-lesioned and l-DOPA-treated (6-OHDA/l-DOPA) rats. KEY

resultsLocal buspirone inhibited SNr neuron activity in all groups. However, systemic buspirone reduced burst activity in 6-OHDA-lesioned rats (with or without l-DOPA treatment), whereas 8-OH-DPAT, a full 5-HT CONCLUSIONS AND IMPLICATIONS: The effects of buspirone in SNr are influenced by dopamine loss and l-DOPA treatment. The present results suggest that the regulation of burst activity of the SNr induced by DA loss may be a good target to test new drugs for the treatment of PD and LID.

Indexed as

LevodopaPars ReticulataAnimalsAntiparkinson AgentsBuspironeDopamineOxidopamineRatsSubstantia NigraAntiparkinson AgentsBuspironeDopamineLevodopaOxidopamine

Identifiers

PMID32464686
PMCPMC7429490
OpenAlexW3029354427

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.