Evidence map›Paper›PMID 39238384›Full record

ArticleCurrent pharmaceutical biotechnology2025

Pedro Cruz de Oliveira Junior, Eliana Janet Sanjinez-Argandona, Janaine Alberto Marangoni Faoro, Rosilda Mara Mussury Franco Silva, Elisabete Castelon Konkiewitz, Edward Benjamin Ziff, Marcia Regina Pereira Cabral, Maria Helena Sarragiotto, Gisele de Freitas Gauze, Andrew Matheus Frederico Rozada and 3 more

Abstract read
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Article in Current pharmaceutical biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Pedro Cruz de Oliveira JuniorCollege of Biological and Environmental Sciences, Federal University of Grande Dourados, MS, Brazil.
Eliana Janet Sanjinez-ArgandonaCollege of Biological and Environmental Sciences, Federal University of Grande Dourados, MS, Brazil.
Janaine Alberto Marangoni FaoroCollege of Health Science, Federal University of Grande Dourados, Dourados, MS, Brazil.
Rosilda Mara Mussury Franco SilvaCollege of Biological and Environmental Sciences, Federal University of Grande Dourados, MS, Brazil.
Elisabete Castelon KonkiewitzCollege of Health Science, Federal University of Grande Dourados, Dourados, MS, Brazil.
Edward Benjamin ZiffNew York University, Department of Biochemistry and Molecular Pharmacology, NYU Grossman School of Medicine, New York City, New York, United States.
Marcia Regina Pereira CabralDepartment of Chemistry, State University of Maringá UEM, Maringá, Paraná, Brazil.
Maria Helena SarragiottoDepartment of Chemistry, State University of Maringá UEM, Maringá, Paraná, Brazil.
Gisele de Freitas GauzeDepartment of Chemistry, State University of Maringá UEM, Maringá, Paraná, Brazil.
Andrew Matheus Frederico RozadaDepartment of Chemistry, State University of Maringá UEM, Maringá, Paraná, Brazil.
Luciane Mendes MonteiroPostgraduate Program in Pharmaceutical Sciences, State University of Ponta Grossa, Ponta Grossa, Paraná, Brazil.
Jane ManfronPostgraduate Program in Pharmaceutical Sciences, State University of Ponta Grossa, Ponta Grossa, Paraná, Brazil.
Anelise Samara Nazari FormagioCollege of Health Science, Federal University of Grande Dourados, Dourados, MS, Brazil.

Funding

CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Brazil) 2764/2011, 635033/2021-00
6 · The paper itself

Abstract

background

objectivesThis study evaluated the neurobehavioural effects of an ethanolic extract of

methodsEEGV was investigated by UHPLC‒MS/MS and dereplication and molecular network were investigated using platforms available for natural product chemistry. For the

resultsSecoxyloganin, grandifloroside, hyperin/or isoquercitrin, uncaric acid and ursolic acid were identified by UHPLC‒MS/MS. Molecular networking by three flavonoids, three triterpenes, two coumarins, two iridoids, and one phenolic acid. EEGV reversed these scopolamineinduced effects. In the forced swim and tail suspension test, EEGV (30 and 100 mg/kg) significantly reduced the immobility time. EEGV significantly reduced the number of buried marbles, while in the elevated plus maze test, no changes were observed compared to the Sco group. AChE activity was altered in the hippocampus. Studies of the molecular coupling of iridoid glycosides (grandifloroside and secoxyloganin) and flavonoid hyperin with AChE revealed significant interactions, corroborating the activity indicated by the inhibition assay.

conclusionThese results might be in accordance with medicinal use for neuroprotetor effects and important microchemical and micromorphological data that support the identification and quality control of

Indexed as

Neuroprotective AgentsPlant ExtractsAnimalsBehavior, AnimalBrainMaleMaze LearningMiceMolecular Docking SimulationPlant LeavesPlant StemsNeuroprotective AgentsPlant Extractsacetylcholinesterasemicromorphologicalmolecular dockingscopolamine“Veludinho do campo”X-ray spectroscopy.

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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.