Evidence map›Paper›PMID 29021710›Full record

ArticleJournal of ginseng research2017

Melanogenesis inhibition activity of floralginsenoside A from

Dae Young Lee, Jongsung Lee, Yong Tae Jeong, Geon Hee Byun, Jin Hee Kim

Open access · goldAbstract read
In one paragraph

Article in Journal of ginseng research, 2017. 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
1.5field-weighted citation impact, top 20% 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, 37 citations in OpenAlex.

  1. Review
  2. Therapeutic Applications of Ginseng Natural Compounds for Health Management.International journal of molecular sciences · 2023
    Review
  3. The Potential ofAntioxidants (Basel, Switzerland) · 2023
    Article
  4. Article
  5. Review
  6. Natural products in cosmetics.Natural products and bioprospecting · 2022
    Review
  7. Review
  8. Review
  9. Anti-melanogenic property of ginsenoside Rf fromJournal of ginseng research · 2021
    Article
  10. Article
  11. Anti-Pigmentary Natural Compounds and Their Mode of Action.International journal of molecular sciences · 2021
    Review
  12. Article
  13. Advances in Saponin Diversity ofMolecules (Basel, Switzerland) · 2020
    Review
  14. Review
  15. Article
  16. Article
  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

5 authors at 5 institutions in 1 country.

Dae Young LeeDepartment of Herbal Crop Research, National Institute of Horticultural and Herbal Science, RDA, Eumseong, Republic of Korea.
Jongsung LeeDepartment of Genetic Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Yong Tae JeongFreshwater Bioresources Utilization Division, Nakdonggang National Institute of Biological Resources, SangJu, Republic of Korea.
Geon Hee ByunCollege of Pharmacy, Kyungpook National University, Daegu, Republic of Korea.
Jin Hee KimCollege of Herbal Bio-industry, Daegu Haany University, Gyeongsan, Republic of Korea.
Daegu Haany University · KRKyungpook National University · KRNational Institute of Biological Resources · KRRural Development Administration · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background

methodsChemical structures of FGA, GRD, and GRE were determined based on spectroscopic methods, including fast atom bombardment mass spectroscopy, ID-nuclear magnetic resonance, and infrared spectroscopy. Inhibitory activities of these compounds on melanogenesis were studied by measuring the expression of protein and melanin content in the melan-a cell line. This inhibitory activity was confirmed by observing pigmentation and tyrosinase activities of zebrafish.

resultsGRD, GRE, and FGA were not cytotoxic at concentrations less than 20μM, 80μM, and 160μM in melan-a cells, respectively. GRD, GRE, and FGA inhibited melanin biosynthesis in melan-a cells by 15.2%, 22.9%, and 23.9% at 20μM, 80μM, and 160μM, respectively. FGA was observed to display the most potent inhibitory effect. In addition, FGA decreased microphthalmia-associated transcription factor protein expression in a dose-dependent manner. Moreover, FGA induced extracellular signal-regulated kinase phosphorylation level in melan-a cells. In addition, melanin pigment content and tyrosinase activity in zebrafish treated with FGA at160μM were reduced.

conclusionFGA showed the most potent inhibition of melanogenesis in both

Indexed as

antimelanogenesisfloralginsenoside APanax ginseng berry

Identifiers

PMID29021710
PMCPMC5628341
OpenAlexW2602074525

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.