Evidence map›Paper›PMID 23054587›Full record

ArticleJournal of molecular neuroscience : MN2013

Protective effects of ascorbic acid on behavior and oxidative status of restraint-stressed mice.

Morgana Moretti, Josiane Budni, Danubia Bonfanti Dos Santos, Alessandra Antunes, Juliana Felipe Daufenbach, Luana Meller Manosso, Marcelo Farina, Ana Lúcia S Rodrigues

Abstract read
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In one paragraph

Article in Journal of molecular neuroscience : MN, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

32 citing papers in PubMed, 92 citations in OpenAlex.

  1. Trial
  2. Review
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  13. Physical exercise prevents amyloid βMetabolic brain disease · 2021
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  14. Journal of blood medicine · 2021
    Article
  15. Vitamin C, Pain and Opioid Use Disorder.Integrative medicine (Encinitas, Calif.) · 2020
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Antistress Effects ofOxidative medicine and cellular longevity · 2019
    Article
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 1 institution in 1 country.

Morgana MorettiDepartamento de Bioquímica, Centro de Ciências Biológicas, Universidade Federal de Santa Catarina, Florianópolis, 88040-900 SC, Brazil.
Josiane Budni
Danubia Bonfanti Dos Santos
Alessandra Antunes
Juliana Felipe Daufenbach
Luana Meller Manosso
Marcelo Farina
Ana Lúcia S Rodrigues
Universidade Federal de Santa Catarina · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies have demonstrated an association between stressful conditions and the onset of clinical depression. Considering the antidepressant-like properties of ascorbic acid in both experimental and clinical approaches, we evaluated the beneficial effect of this vitamin on restraint stress-induced behavioral and neurochemical alterations. Acute restraint stress caused a depressive-like behavior in the forced swimming test, accompanied by increased lipid peroxidation (cerebral cortex and hippocampus); increased superoxide dismutase (cerebral cortex and hippocampus), glutathione reductase (cerebral cortex), and glutathione peroxidase (cerebral cortex and hippocampus) activities; and elevated expression of Bcl-2 (hippocampus). Oral administration of ascorbic acid (1 mg/kg) or fluoxetine (10 mg/kg) 1 h before restraint stress prevented the stress-induced increase on immobility time in the forced swimming test. Moreover, this vitamin reduced lipid peroxidation to control levels and restored the activity of superoxide dismutase, glutathione reductase, and glutathione peroxidase. Ascorbic acid had no effect on the increased level of Bcl-2 induced by stress. Glutathione levels, glycogen synthase kinase-3β phosphorylation, and Bax expression were not altered by stress or ascorbic acid administration. Besides reinforcing the antioxidant potential of ascorbic acid, our results support the notion that oxidative stress plays a role in the pathogenesis and treatment of stress-induced depression.

Indexed as

AnimalsAntioxidantsAscorbic Acidbcl-2-Associated X ProteinCerebral CortexDepressive DisorderFemaleGlutathione PeroxidaseGlutathione ReductaseGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaHippocampusLipid MetabolismMiceMotor ActivityOxidation-ReductionAntioxidantsAscorbic AcidBax protein, mousebcl-2-Associated X ProteinBcl2 protein, mouseGlutathione PeroxidaseGlutathione ReductaseGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGsk3b protein, mouseProto-Oncogene Proteins c-bcl-2Superoxide DismutaseVitamins

Identifiers

PMID23054587
OpenAlexW2096456417

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.