Evidence map›Paper›PMID 26578955›Full record

ReviewFrontiers in pharmacology2015

Ginseng pharmacology: a new paradigm based on gintonin-lysophosphatidic acid receptor interactions.

Sun-Hye Choi, Seok-Won Jung, Byung-Hwan Lee, Hyeon-Joong Kim, Sung-Hee Hwang, Ho-Kyoung Kim, Seung-Yeol Nah

Abstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

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

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Gintonin-EnrichedCurrent issues in molecular biology · 2024
    Article
  9. Review
  10. The impact of the administration of red ginseng (Frontiers in veterinary science · 2024
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Gintonin, aJournal of ginseng research · 2023
    Article
  17. Article
  18. Article
  19. Nrf2 Pathway in Huntington's Disease (HD): What Is Its Role?International journal of molecular sciences · 2022
    Review
  20. Visualization of the binding between gintonin, aJournal of ginseng research · 2022
    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

7 authors.

Sun-Hye ChoiGinsentology Research Laboratory, Department of Physiology, College of Veterinary Medicine, Konkuk University , Seoul, South Korea.
Seok-Won JungGinsentology Research Laboratory, Department of Physiology, College of Veterinary Medicine, Konkuk University , Seoul, South Korea.
Byung-Hwan LeeGinsentology Research Laboratory, Department of Physiology, College of Veterinary Medicine, Konkuk University , Seoul, South Korea.
Hyeon-Joong KimGinsentology Research Laboratory, Department of Physiology, College of Veterinary Medicine, Konkuk University , Seoul, South Korea.
Sung-Hee HwangDepartment of Pharmaceutical Engineering, Sangji University , Wonju, South Korea.
Ho-Kyoung KimMibyeong Research Center, Korea Institute of Oriental Medicine , Daejeon, South Korea.
Seung-Yeol NahGinsentology Research Laboratory, Department of Physiology, College of Veterinary Medicine, Konkuk University , Seoul, South Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ginseng, the root of Panax ginseng, is used as a traditional medicine. Despite the long history of the use of ginseng, there is no specific scientific or clinical rationale for ginseng pharmacology besides its application as a general tonic. The ambiguous description of ginseng pharmacology might be due to the absence of a predominant active ingredient that represents ginseng pharmacology. Recent studies show that ginseng abundantly contains lysophosphatidic acids (LPAs), which are phospholipid-derived growth factor with diverse biological functions including those claimed to be exhibited by ginseng. LPAs in ginseng form a complex with ginseng proteins, which can bind and deliver LPA to its cognate receptors with a high affinity. As a first messenger, gintonin produces second messenger Ca(2+) via G protein-coupled LPA receptors. Ca(2+) is an intracellular mediator of gintonin and initiates a cascade of amplifications for further intercellular communications by activation of Ca(2+)-dependent kinases, receptors, gliotransmitter, and neurotransmitter release. Ginsenosides, which have been regarded as primary ingredients of ginseng, cannot elicit intracellular [Ca(2+)]i transients, since they lack specific cell surface receptor. However, ginsenosides exhibit non-specific ion channel and receptor regulations. This is the key characteristic that distinguishes gintonin from ginsenosides. Although the current discourse on ginseng pharmacology is focused on ginsenosides, gintonin can definitely provide a mode of action for ginseng pharmacology that ginsenosides cannot. This review article introduces a novel concept of ginseng ligand-LPA receptor interaction and proposes to establish a paradigm that shifts the focus from ginsenosides to gintonin as a major ingredient representing ginseng pharmacology.

Indexed as

ginsengginseng pharmacologygintoninG protein-coupled LPA receptorsLPAsnew paradigm

Identifiers

PMID26578955
PMCPMC4621423

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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.