Evidence map›Paper›PMID 32148404›Full record

ArticleJournal of ginseng research2020

Tolerability and pharmacokinetics of ginsenosides Rb1, Rb2, Rc, Rd, and compound K after single or multiple administration of red ginseng extract in human beings.

Min-Koo Choi, Sojeong Jin, Ji-Hyeon Jeon, Woo Youl Kang, Sook Jin Seong, Young-Ran Yoon, Yong-Hae Han, Im-Sook Song

Abstract read
In one paragraph

Article in Journal of ginseng research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

40 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Nutrients · 2026
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  11. Potential ofChinese herbal medicines · 2025
    Review
  12. Journal of ginseng research · 2025
    Review
  13. Article
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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

8 authors.

Min-Koo ChoiCollege of Pharmacy, Dankook University, Cheon-an, Republic of Korea.
Sojeong JinCollege of Pharmacy, Dankook University, Cheon-an, Republic of Korea.
Ji-Hyeon JeonResearch Institute of Pharmaceutical Sciences and College of Pharmacy, Kyungpook National University, Daegu, Republic of Korea.
Woo Youl KangClinical Trial Center, Kyungpook National University Hospital, Daegu, Republic of Korea.
Sook Jin SeongDepartment of Biomedical Science, BK21 Plus KNU Bio-Medical Convergence Program for Creative Talent, Graduate School, Kyungpook National University, Daegu, Republic of Korea.
Young-Ran YoonClinical Trial Center, Kyungpook National University Hospital, Daegu, Republic of Korea.
Yong-Hae HanLife Science Institute, Daewoong Pharmaceutical, Yongin, Gyeonggi-do, Republic of Korea.
Im-Sook SongResearch Institute of Pharmaceutical Sciences and College of Pharmacy, Kyungpook National University, Daegu, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe investigated the tolerability and pharmacokinetic properties of various ginsenosides, including Rb1, Rb2, Rc, Rd, and compound K, after single or multiple administrations of red ginseng extract in human beings.

methodsRed ginseng extract (dried ginseng > 60%) was administered once and repeatedly for 15 days to 15 healthy Korean people. After single and repeated administration of red ginsengextract, blood sample collection, measurement of blood pressure and body temperature, and routine laboratory test were conducted over 48-h test periods.

resultsRepeated administration of high-dose red ginseng for 15 days was well tolerated and did not produce significant changes in body temperature or blood pressure. The plasma concentrations of Rb1, Rb2, and Rc were stable and showed similar area under the plasma concentration-time curve (AUC) values after 15 days of repeated administration. Their AUC values after repeated administration of red ginseng extract for 15 days accumulated 4.5- to 6.7-fold compared with single-dose AUC. However, the plasma concentrations of Rd and compound K showed large interindividual variations but correlated well between AUC of Rd and compound K. Compound K did not accumulate after 15 days of repeated administration of red ginseng extract.

conclusionA good correlation between the AUC values of Rd and compound K might be the result of intestinal biotransformation of Rb1, Rb2, and Rc to Rd and subsequently to compound K, rather than the intestinal permeability of these ginsenosides. A strategy to increase biotransformation or reduce metabolic intersubject variability may increase the plasma concentrations of Rd and compound K.

Indexed as

apical to basal, A to Bapparent permeability, Papparea under the plasma concentration-time curve, AUCbasal to apical, B to AginsenosidesHank's balanced salt solution, HBSSliquid chromatography-tandem mass spectrometry, LC-MS/MSmaximum plasma concentration, CmaxMRT, mean residence timemultiple reaction monitoring, MRMpharmacokineticsred ginsengsingle and repeated administrationt1/2, elimination half-lifetime to reach Cmax, Tmaxtolerability

Identifiers

PMID32148404
PMCPMC7031742

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Registered trials

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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.