Evidence map›Paper›PMID 29949107›Full record

ArticleNeurotoxicity research2018

Comparing the Effects of Ferulic Acid and Sugarcane Aqueous Extract in In Vitro and In Vivo Neurotoxic Models.

Aline Colonnello, Ilan Kotlar, María Eduarda de Lima, Alma Ortíz-Plata, Rodolfo García-Contreras, Félix Alexandre Antunes Soares, Michael Aschner, Abel Santamaría

Abstract read
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In one paragraph

Article in Neurotoxicity research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. 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 5 institutions in 3 countries.

Aline ColonnelloLaboratorio de Aminoácidos Excitadores, Instituto Nacional de Neurología y Neurocirugía, 14269, Mexico City, Mexico.
Ilan KotlarLaboratorio de Aminoácidos Excitadores, Instituto Nacional de Neurología y Neurocirugía, 14269, Mexico City, Mexico.
María Eduarda de LimaLaboratorio de Aminoácidos Excitadores, Instituto Nacional de Neurología y Neurocirugía, 14269, Mexico City, Mexico.
Alma Ortíz-PlataLaboratorio de Patología Experimental, Instituto Nacional de Neurología y Neurocirugía, 14269, Mexico City, Mexico.
Rodolfo García-ContrerasDepartamento de Microbiología y Parasitología, Facultad de Medicina, Universidad Nacional Autónoma de México, 04510, Mexico City, Mexico.
Félix Alexandre Antunes SoaresDepartamento de Bioquimica e Biologia Molecular, CCNE, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil.
Michael AschnerDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Abel SantamaríaLaboratorio de Aminoácidos Excitadores, Instituto Nacional de Neurología y Neurocirugía, 14269, Mexico City, Mexico. absada@yahoo.com.
Instituto Nacional de Neurología y Neurocirugía · MXUniversidad Nacional Autónoma de México · MXAlbert Einstein College of Medicine · USUniversidade Federal de Santa Maria · BRUniversidade Federal do Pampa · BR

Funding

National Institutes of Health NIEHS R01ES020852National Institutes of Health NIEHS R01ES07331National Institutes of Health NIEHS R01ES10563
6 · The paper itself

Abstract

Molecules exhibiting antioxidant, neuroprotective, and regulatory properties inherent to natural products consumed by humans are gaining attention in biomedical research. Ferulic acid (FA) is a phenolic compound possessing antioxidant and cytoprotective properties. It is found in several vegetables, including sugarcane, where it serves as the main antioxidant component. Here, we compared the antioxidant and cytoprotective effects of FA with those of the total sugarcane aqueous extract (SCAE). Specifically, we assessed biochemical markers of cell dysfunction in rat cortical brain slices and markers of physiological stress in Caenorhabditis elegans upon exposure to toxins evoking different mechanisms of neurotoxicity, including direct oxidative stress and/or excitotoxicity. In rat cortical slices, FA (250 and 500 μM), but not SCAE (~ 270 μM of total polyphenols), prevented the loss of reductive capacity induced by the excitotoxin quinolinic acid (QUIN, 100 μM), the pro-oxidant agent ferrous sulfate (FeSO

Indexed as

Analysis of VarianceAnimalsAnimals, Genetically ModifiedBirth RateCaenorhabditis elegansCaenorhabditis elegans ProteinsCerebral CortexCoumaric AcidsDisease Models, AnimalFerrous CompoundsIn Vitro TechniquesIronLocomotionMaleNeurotoxicity SyndromesOxidopamineCaenorhabditis elegans ProteinsCoumaric AcidsFerrous Compoundsferrous sulfateferulic acidIronOxidopaminePlant ExtractsQuinolinic AcidAntioxidant defenseC. elegansFerulic acidNeurotoxic modelsProtective effectsRat cortical slicesSugarcane

Identifiers

PMID29949107
OpenAlexW2808401043

What OpenQuestion holds

Textmetadata
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.