Evidence map›Paper›PMID 25978330›Full record

ArticlePloS one2015

The Protecting Effect of Deoxyschisandrin and Schisandrin B on HaCaT Cells against UVB-Induced Damage.

Wei Hou, Wei Gao, Datao Wang, Qingxiu Liu, Siwen Zheng, Yingping Wang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-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

18 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Antioxidant Effects ofAntioxidants (Basel, Switzerland) · 2021
    Review
  7. Article
  8. Review
  9. Article
  10. Potential ofNutrients · 2019
    Review
  11. Effects of Deoxyschisandrin on Visceral Sensitivity of Mice with Inflammatory Bowel Disease.Evidence-based complementary and alternative medicine : eCAM · 2019
    Article
  12. Long non-coding RNA HOTAIR promotes UVB-induced apoptosis and inflammatory injury by up-regulation of PKR in keratinocytes.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2018
    Article
  13. Article
  14. Article
  15. Article
  16. Current knowledge ofPhytochemistry reviews : proceedings of the Phytochemical Society of Europe · 2017
    Review
  17. Article
  18. Review
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

6 authors at 2 institutions in 1 country.

Wei HouInstitute of Special Animal and Plant Sciences, Chinese Academy of Agricultural Sciences, Changchun, China.
Wei GaoInstitute of Special Animal and Plant Sciences, Chinese Academy of Agricultural Sciences, Changchun, China.
Datao WangInstitute of Special Animal and Plant Sciences, Chinese Academy of Agricultural Sciences, Changchun, China.
Qingxiu LiuInstitute of Special Animal and Plant Sciences, Chinese Academy of Agricultural Sciences, Changchun, China.
Siwen ZhengInstitute of Special Animal and Plant Sciences, Chinese Academy of Agricultural Sciences, Changchun, China.
Yingping WangInstitute of Special Animal and Plant Sciences, Chinese Academy of Agricultural Sciences, Changchun, China.
Chinese Academy of Agricultural Sciences · CNInstitute of Special Animal and Plant Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schisandra chinensis is a traditional Chinese medicine that has multiple biological activities, including antioxidant, anticancer, tonic, and anti-aging effects. Deoxyschisandrin (SA) and schisandrin B (SB), the two major lignans isolated from S. chinensis, exert high antioxidant activities in vitro and in vivo by scavenging free radicals, such as reactive oxygen species (ROS). Ultraviolet B-ray (UVB) radiation induces the production of ROS and DNA damage, which eventually leads to cell death by apoptosis. However, it is unknown whether SA or SB protects cells against UVB-induced cellular DNA damage. Our study showed that both SA and SB effectively protected HaCaT cells from UVB-induced cell death by antagonizing UVB-mediated production of ROS and induction of DNA damage. Our results showed that both SA and SB significantly prevented UVB-induced loss of cell viability using 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assays. Dichloro-dihydro-fluorescein diacetate (DCFH-DA) assays showed that the production of ROS following UVB exposure was inhibited by treatment with SA and SB. Moreover, SA and SB decreased the UVB-induced DNA damage in HaCaT cells by comet assays. In addition, SA and SB also prevented UVB-induced cell apoptosis and the cleavage of caspase-3, caspase-8 and caspase-9. In a word, our results imply that the antioxidants SA and SB could protect cells from UVB-induced cell damage via scavenging ROS.

Indexed as

AntioxidantsApoptosisCaspasesCell LineCell SurvivalCyclooctanesCytoprotectionDNA DamageHumansKeratinocytesLignansPolycyclic CompoundsReactive Oxygen SpeciesSchisandraUltraviolet RaysAntioxidantsCaspasesCyclooctanesLignansPolycyclic CompoundsReactive Oxygen Speciesschizandrin Aschizandrin B

Identifiers

PMID25978330
PMCPMC4433126
OpenAlexW982251741

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.