Evidence map›Paper›PMID 30906501›Full record

ArticleOxidative medicine and cellular longevity2019

Relation of Redox and Structural Alterations of Rat Skin in the Function of Chronological Aging.

Aleksandra Jankovic, Luciano Saso, Aleksandra Korac, Bato Korac

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. 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

4 authors at 2 institutions in 2 countries.

Aleksandra JankovicInstitute for Biological Research "Sinisa Stankovic", University of Belgrade, Serbia.ORCID 0000-0002-6945-927X
Luciano SasoDepartment of Physiology and Pharmacology "Vittorio Erspamer", Faculty of Pharmacy and Medicine, Sapienza University of Rome, Italy.ORCID 0000-0003-4530-8706
Aleksandra KoracFaculty of Biology, University of Belgrade, Serbia.ORCID 0000-0002-3044-9963
Bato KoracInstitute for Biological Research "Sinisa Stankovic", University of Belgrade, Serbia.ORCID 0000-0001-5272-579X
University of Belgrade · RSSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulation of oxidative insults on molecular and supramolecular levels could compromise renewal potency and architecture in the aging skin. To examine and compare morphological and ultrastructural changes with redox alterations during chronological skin aging, activities of antioxidant defense (AD) enzymes, superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), glutathione reductase (GR), thioredoxin reductase (TR), and methionine sulfoxide reductase A (MsrA), and the markers of oxidative damage of biomolecules-4-hydroxynonenal (HNE) and 8-oxoguanine (8-oxoG)-were examined in the rat skin during life (from 3 days to 21 months). As compared to adult 3-month-old skin, higher activities of CAT, GSH-Px, and GR and a decline in expression of MsrA are found in 21-month-old skin. These changes correspond to degenerative changes at structural and ultrastructural levels in epidermal and dermal compartments, low proliferation capacity, and higher levels of HNE-modified protein aldehydes (particularly in basal lamina) and 8-oxoG positivity in nuclei and mitochondria in the sebaceous glands and root sheath. In 3-day-old skin, higher activities of AD enzymes (SOD, CAT, GR, and TR) and MsrA expression correspond to intensive postnatal development and proliferation. In contrast to 21-month-old skin, a high level of HNE in young skin is not accompanied by 8-oxoG positivity or any morphological disturbances. Observed results indicate that increased activity of AD enzymes in elderly rat skin represents the compensatory response to accumulated oxidative damage of DNA and proteins, accompanied by attenuated repair and proliferative capacity, but in young rats the redox changes are necessary and inherent with processes which occur during postnatal skin development. Мorphological and ultrastructurаl changes are in line with the redox profile in the skin of young and old rats.

Indexed as

8-Hydroxy-2'-DeoxyguanosineAgingAldehydesAnimalsCatalaseCell ProliferationCollagenDeoxyguanosineDNA DamageFibroblastsGlutathione PeroxidaseGlutathione ReductaseMaleOxidation-ReductionOxidoreductasesProliferating Cell Nuclear Antigen4-hydroxy-2-nonenal8-Hydroxy-2'-DeoxyguanosineAldehydesCatalaseCollagenDeoxyguanosineGlutathione PeroxidaseGlutathione ReductaseMsrA protein, ratOxidoreductasesProliferating Cell Nuclear AntigenSuperoxide DismutaseThioredoxin-Disulfide Reductase

Identifiers

PMID30906501
PMCPMC6393874
OpenAlexW2912583419

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.