Evidence map›Paper›PMID 30976171›Full record

ArticleJournal of ginseng research2019

Ginsenoside Rb2 suppresses the glutamate-mediated oxidative stress and neuronal cell death in HT22 cells.

Dong Hoi Kim, Dae Won Kim, Bo Hyun Jung, Jong Hun Lee, Heesu Lee, Gwi Seo Hwang, Ki Sung Kang, Jae Wook Lee

Open access · goldAbstract read
In one paragraph

Article in Journal of ginseng research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

42 citing papers in PubMed, 82 citations in OpenAlex.

  1. Review
  2. Review
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  4. Article
  5. Review
  6. Review
  7. Mechanism of ginsenoside RbBiomedical reports · 2024
    Article
  8. Neuroprotective Effects of Ethanol ExtractInternational journal of molecular sciences · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Therapeutic Applications of Ginseng Natural Compounds for Health Management.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Neuroprotective Effects of Ethanol Extract ofInternational journal of molecular sciences · 2023
    Article
  20. 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.

Dong Hoi KimConvergence Research Center for Dementia, KIST, Seoul, Republic of Korea.
Dae Won KimDepartment of Biochemistry, College of Dentistry, Gangneung Wonju National University, Gangneung, Republic of Korea.
Bo Hyun JungDepartment of Oral Anatomy, College of Dentistry, Gangneung Wonju National University, Gangneung, Republic of Korea.
Jong Hun LeeDepartment of Oral Anatomy, College of Dentistry, Gangneung Wonju National University, Gangneung, Republic of Korea.
Heesu LeeDepartment of Oral Anatomy, College of Dentistry, Gangneung Wonju National University, Gangneung, Republic of Korea.
Gwi Seo HwangCollege of Korean Medicine, Gacheun University, Seongnam, Republic of Korea.
Ki Sung KangCollege of Korean Medicine, Gacheun University, Seongnam, Republic of Korea.
Jae Wook LeeConvergence Research Center for Dementia, KIST, Seoul, Republic of Korea.
Gangneung–Wonju National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe objective of our study was to analyze the neuroprotective effects of ginsenoside derivatives Rb1, Rb2, Rc, Rd, Rg1, and Rg3 against glutamate-mediated neurotoxicity in HT22 hippocampal mouse neuron cells.

methodsThe neuroprotective effect of ginsenosides were evaluated by measuring cell viability. Protein expressions of mitogen-activated protein kinase (MAPK), Bcl2, Bax, and apoptosis-inducing factor (AIF) were determined by Western blot analysis. The occurrence of apoptotic and death cells was determined by flow cytometry. Cellular level of Ca

resultReduction of cell viability by glutamate (5 mM) was significantly suppressed by treatment with ginsenoside Rb2. Phosphorylation of MAPKs, Bax, and nuclear AIF was gradually increased by treatment with 5 mM of glutamate and decreased by co-treatment with Rb2. The occurrence of apoptotic cells was decreased by treatment with Rb2 (25.7 μM). Cellular Ca

conclusionOur results suggest that Rb2 possesses neuroprotective properties that suppress glutamate-induced neurotoxicity. The molecular mechanism of Rb2 is by suppressing the MAPKs activity and AIF translocation.

Indexed as

Ginsenoside Rb2MAPKNeurotoxicityReactive oxygen species

Identifiers

PMID30976171
PMCPMC6437470
OpenAlexW2904108713

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.