Evidence map›Paper›PMID 34271100›Full record

ArticleThe Journal of nutritional biochemistry2021

Dietary supplementation with sulforaphane ameliorates skin aging through activation of the Keap1-Nrf2 pathway.

Marija Petkovic, Ermelindo C Leal, Ines Alves, Chanda Bose, Philip T Palade, Preeti Singh, Sanjay Awasthi, Elisabet Børsheim, Louise T Dalgaard, Sharda P Singh and 1 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of nutritional biochemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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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

11 authors at 5 institutions in 3 countries.

Marija PetkovicDepartment of Science and Environment, Roskilde University, Roskilde, Denmark; Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal; Institute for Interdisciplinary Research, University of Coimbra, Coimbra, Portugal.
Ermelindo C LealCenter for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal; Institute for Interdisciplinary Research, University of Coimbra, Coimbra, Portugal.
Ines AlvesCenter for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.
Chanda BoseDepartment of Internal Medicine, Division of Hematology and Oncology Texas Tech University Medical Sciences Center, Lubbock, Texas, USA.
Philip T PaladeDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Preeti SinghDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Sanjay AwasthiDepartment of Internal Medicine, Division of Hematology and Oncology Texas Tech University Medical Sciences Center, Lubbock, Texas, USA.
Elisabet BørsheimDepartment of Pediatrics, University of Arkansas for Medical Sciences; Arkansas Children's Research Institute, Little Rock, AR, USA; Department of Geriatrics, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Louise T DalgaardDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.
Sharda P SinghDepartment of Internal Medicine, Division of Hematology and Oncology Texas Tech University Medical Sciences Center, Lubbock, Texas, USA; Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, AR, USA. Electronic address: sharda.singh@ttuhsc.edu.
Eugenia CarvalhoCenter for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal; Institute for Interdisciplinary Research, University of Coimbra, Coimbra, Portugal; Department of Geriatrics, University of Arkansas for Medical Sciences, Little Rock, AR, USA. Electronic address: ecarvalh@cnc.uc.pt.
Texas Tech University · USUniversity of Coimbra · PTRoskilde University · DKUniversity of Arkansas for Medical Sciences · USArkansas Children's Hospital · US

Funding

RESOURCE CORE 3: ANALYTICAL COREP30AG028718 · NIA · UNIV OF ARKANSAS FOR MED SCIS · PI WEI, JEANNE Y · 2011 to 2015
$5.1M
Effects of amino acids on regional lipid metabolismR01AG033761 · NIA · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BORSHEIM, ELISABET · 2009 to 2013
$1.6M
Causative role of lipid peroxidation products in obesity and agingR01AG032643 · NIA · UNIV OF ARKANSAS FOR MED SCIS · PI SINGH, SHARDA P · 2009 to 2013
$1.2M
STUDIES IN MATHEMATICS AND STATISTICSZ01CT000024 · CIT · COMPUTER RESEARCH AND TECHNOLOGY · PI WEISS, GEORGE H · 1985 to 2008
$408k
Intramural NIH HHS Z01 CT000024NIA NIH HHS P30 AG028718NIA NIH HHS R01 AG032643NIA NIH HHS R01 AG033761
6 · The paper itself

Abstract

Visible impairments in skin appearance, as well as a subtle decline in its functionality at the molecular level, are hallmarks of skin aging. Activation of the nuclear factor (erythroid-derived 2)-like 2 (Nrf2)-pathway, which is important in controlling inflammation and oxidative stress that occur during aging, can be triggered by sulforaphane (SFN), an isothiocyanate found in plants from the Brassicaceae family. This study aimed to assess the effects of SFN intake on age-related skin alterations. Male C57BL6 young (2 months) and old (21 months) mice were treated for 3 months with SFN diet (442.5 mg per kg) or control diet. The antioxidant capacities of the skin were increased in old SFN-treated animals as measured by mRNA levels of Nrf2 (P<.001) and its target genes NQO1 (P<.001) and HO1 (P<.01). Protein expression for Nrf2 was also increased in old SFN fed animals (P<.01), but not the protein expression of NQO1 or HO1. Additionally, ROS and MMP9 protein levels were significantly decreased (P<.05) in old SFN fed animals. Histopathological analysis confirmed that there was no difference in epidermal thickness in old, when compared to young, SFN treated animals, while the dermal layer thickness was lower in old vs. young, treated animals (P<.05). Moreover, collagen deposition was improved with SFN treatment in young (P<.05) and structurally significantly improved in the old mice (P<.001). SFN dietary supplementation therefore ameliorates skin aging through activation of the Nrf2-pathway.

Indexed as

AnimalsAntioxidantsDietary SupplementsInflammationIsothiocyanatesKelch-Like ECH-Associated Protein 1MaleMatrix Metalloproteinase 9MiceMice, Inbred C57BLNF-E2-Related Factor 2Oxidative StressReactive Oxygen SpeciesSkin AgingSulfoxidesAntioxidantsIsothiocyanatesKelch-Like ECH-Associated Protein 1Matrix Metalloproteinase 9NF-E2-Related Factor 2Reactive Oxygen SpeciessulforaphaneSulfoxidesCruciferous vegetablesNrf2 pathwayoxidative stressskin agingsulforaphane

Identifiers

PMID34271100
PMCPMC10580548
OpenAlexW3182714007

What OpenQuestion holds

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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.