Evidence map›Paper›PMID 28391182›Full record

ArticleRedox biology2017

Tert-buthylhydroquinone pre-conditioning exerts dual effects in old female rats exposed to 3-nitropropionic acid.

Alejandro Silva-Palacios, Ana L Colín-González, Stefanie P López-Cervantes, Cecilia Zazueta, Armando Luna-López, Abel Santamaría, Mina Königsberg

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Redox biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

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  8. Nrf2 Pathway in Huntington's Disease (HD): What Is Its Role?International journal of molecular sciences · 2022
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Alejandro Silva-PalaciosDepartamento de Ciencias de la Salud, DCBS, Universidad Autónoma Metropolitana Iztapalapa, Ciudad de México 09340, Mexico; Departamento de Biomedicina Cardiovascular, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, Mexico; Posgrado en Biología Experimental, Universidad Autonomas Metropolitana, Iztapalapa, Ciudad de México, Mexico.
Ana L Colín-GonzálezLaboratorio de Aminoácidos Excitadores, Instituto Nacional de Neurología y Neurocirugía, SSA, Ciudad de México 14269, Mexico.
Stefanie P López-CervantesDepartamento de Ciencias de la Salud, DCBS, Universidad Autónoma Metropolitana Iztapalapa, Ciudad de México 09340, Mexico.
Cecilia ZazuetaDepartamento de Biomedicina Cardiovascular, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, Mexico.
Armando Luna-LópezInstituto Nacional de Geriatría, SSA México, D.F. 14080, Mexico.
Abel SantamaríaLaboratorio de Aminoácidos Excitadores, Instituto Nacional de Neurología y Neurocirugía, SSA, Ciudad de México 14269, Mexico.
Mina KönigsbergDepartamento de Ciencias de la Salud, DCBS, Universidad Autónoma Metropolitana Iztapalapa, Ciudad de México 09340, Mexico. Electronic address: mkf@xanum.uam.mx.
Universidad Autónoma Metropolitana · MXInstituto Nacional de Neurología y Neurocirugía · MXInstituto Nacional de Cardiología · MXInstituto Nacional de Pediatria · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The brain is a very susceptible organ to structural and functional alterations caused by oxidative stress and its vulnerability increases with age. Understanding the antioxidant response activated by the transcription factor Nrf2 has become very important in the aging field in order to activate cellular protection. However, the role of Nrf2 inducers during old age has not been completely understood. Our aim was to activate the Nrf2 pathway by pre-treating old rats with a widely used Nrf2-inducer, tert-buthylhydroquinone (tBHQ), prior to 3-nitropropionic acid (3-NP) insult, in order to evaluate its effects at a behavioral, morphological and biochemical levels. 3-NP has been used to reproduce the biochemical and pathophysiological characteristics of Huntington's disease due to an oxidative effect. Our results suggest that tBHQ confers an important protective effect against 3-NP toxicity; nevertheless, Nrf2 seems not to be the main protective pathway associated to neuroprotection. Hormetic responses include the activation of more than one transcription factor. Nrf2 and NFκB are known to simultaneously initiate different cellular responses against stress by triggering parallel mechanisms, therefore NFκB nuclear accumulation was also evaluated.

Indexed as

AnimalsCell NucleusDisease Models, AnimalFemaleHuntington DiseaseHydroquinonesNeuroprotective AgentsNF-E2-Related Factor 2NF-kappa BNitro CompoundsOxidative StressPropionatesRatsSignal Transduction2-tert-butylhydroquinone3-nitropropionic acidHydroquinonesNeuroprotective AgentsNfe2l2 protein, ratNF-E2-Related Factor 2NF-kappa BNitro CompoundsPropionates3-Nitropropionic acidAgingNrf2 signalingOxidative stressTert-Buthylhydroquinone

Identifiers

PMID28391182
PMCPMC5384325
OpenAlexW2601304286

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.