Evidence map›Paper›PMID 37252278›Full record

ArticleJournal of ginseng research2023

KRG and its major ginsenosides do not show distinct steroidogenic activities examined by the OECD test guideline 440 and 456 assays.

Namkyu Lee, Ju Hyeong Lee, Ji Eun Won, Youn Ji Lee, Sun Hee Hyun, Yeong-Deuk Yi, Gyo In, Hee Dong Han, YoungJoo Lee

Open access · goldAbstract read
In one paragraph

Article in Journal of ginseng research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. The beneficial potential of ginseng for menopause.Journal of ginseng research · 2024
    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

9 authors at 3 institutions in 1 country.

Namkyu LeeDepartment of Integrative Bioscience and Biotechnology, College of Life Science, Sejong University, Seoul, Republic of Korea.
Ju Hyeong LeeDepartment of Immunology, School of Medicine, Konkuk University, Chungcheongbuk-Do, Republic of Korea.
Ji Eun WonDepartment of Immunology, School of Medicine, Konkuk University, Chungcheongbuk-Do, Republic of Korea.
Youn Ji LeeLaboratory of Efficacy Research, Korea Ginseng Corporation, Daejeon, Republic of Korea.
Sun Hee HyunLaboratory of Efficacy Research, Korea Ginseng Corporation, Daejeon, Republic of Korea.
Yeong-Deuk YiLaboratory of Efficacy Research, Korea Ginseng Corporation, Daejeon, Republic of Korea.
Gyo InLaboratory of Efficacy Research, Korea Ginseng Corporation, Daejeon, Republic of Korea.
Hee Dong HanDepartment of Immunology, School of Medicine, Konkuk University, Chungcheongbuk-Do, Republic of Korea.
YoungJoo LeeDepartment of Integrative Bioscience and Biotechnology, College of Life Science, Sejong University, Seoul, Republic of Korea.
Sejong University · KRKonkuk University · KRKorean Society of Ginseng · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Ginseng has been used as a traditional medicine for treatment of many diseases and for general health maintenance. Previously, we showed that ginseng did not demonstrate estrogenic property in ovariectomized mouse model. However, it is still possible that disruption of steroidogenesis leading to indirect hormonal activity. Methods: The hormonal activities were examined in compliance with OECD guidelines for detecting endocrine disrupting chemicals: test guideline (TG) No. 456 (an Results: Korean Red Ginseng (KRG) and ginsenosides Rb1, Rg1, and Rg3 did not interfere with estrogen and testosterone hormone synthesis as examined in H295 cells according to TG 456. KRG treatment to ovariectomized mice did not show a significant change in uterine weight. In addition, serum estrogen and testosterone levels were not change by KRG intake. Conclusion: These results clearly demonstrate that there is no steroidogenic activity associated with KRG and no disruption of the hypothalamic-pituitary-gonadal axis by KRG. Additional tests will be performed in pursuit of cellular molecular targets of ginseng to manifest mode of action.

Indexed as

Ginsenoside Rg1KRGRb1Rg3SteroidogenesisUterotrophic assay

Identifiers

PMID37252278
PMCPMC10214137
OpenAlexW4302010816

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.