Evidence map›Paper›PMID 30976167›Full record

ArticleJournal of ginseng research2019

Nonsaponin fraction of Korean Red Ginseng attenuates cytokine production via inhibition of TLR4 expression.

Huijeong Ahn, Byung-Cheol Han, Jeongeun Kim, Seung Goo Kang, Pyeung-Hyeun Kim, Kyoung Hwa Jang, Seung Ho So, Seung-Ho Lee, Geun-Shik 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  5. CanJournal of ginseng research · 2022
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  15. Characterization of equine inflammasomes and their regulation.Veterinary research communications · 2020
    Article
  16. Effect of hydro-alcoholic extract ofAvicenna journal of phytomedicine
    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

9 authors at 1 institution in 1 country.

Huijeong AhnCollege of Veterinary Medicine and Institute of Veterinary Science, Kangwon National University, Chuncheon, Republic of Korea.
Byung-Cheol HanCollege of Veterinary Medicine and Institute of Veterinary Science, Kangwon National University, Chuncheon, Republic of Korea.
Jeongeun KimCollege of Veterinary Medicine and Institute of Veterinary Science, Kangwon National University, Chuncheon, Republic of Korea.
Seung Goo KangDivision of Biomedical Convergence, College of Biomedical Science, Kangwon National University, Chuncheon, Republic of Korea.
Pyeung-Hyeun KimDepartment of Molecular Bioscience, School of Biomedical Science, Kangwon National University, Chuncheon, Republic of Korea.
Kyoung Hwa JangKorea Ginseng Research Institute, Korea Ginseng Corporation, Daejeon, Republic of Korea.
Seung Ho SoKorea Ginseng Research Institute, Korea Ginseng Corporation, Daejeon, Republic of Korea.
Seung-Ho LeeKorea Ginseng Research Institute, Korea Ginseng Corporation, Daejeon, Republic of Korea.
Geun-Shik LeeCollege of Veterinary Medicine and Institute of Veterinary Science, Kangwon National University, Chuncheon, Republic of Korea.
Kangwon National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGinsenosides of Korean Red Ginseng extracts (RGE) and its saponin components suppress secretion of inflammasome-mediating cytokines, whereas the nonsaponin fraction (NS) of RGE oppositely stimulates cytokine secretion. Although direct exposure of NS to macrophages in mice induces cytokine production, oral administration of NS has not been studied in inflammasome-related disease in animal models.

methodsMice were fed RGE or NS for 7 days and then developed peritonitis. Peritoneal cytokines were measured, and peritoneal exudate cells (PECs) were collected to assay expression levels of a set of toll-like receptors (TLRs) and cytokines in response to NS ingestion. In addition, the role of intestinal bacteria in NS-fed mice was assessed. The effect of preexposure to NS in bone marrow-derived macrophages (BMDMs) on cytokine production was further confirmed.

resultsNS ingestion attenuated secretion of peritoneal cytokines resulting from peritonitis. In addition, the isolated PECs from NS-fed mice presented lower TLR transcription levels than PECs from control diet-fed mice. BMDMs treated with NS showed downregulation of TLR4 mRNA and protein expression, which was mediated by the TLR4-MyD88-NFκB signal pathway. BMDMs pretreated with NS produced less cytokines in response to TLR4 ligands.

conclusionNS administration directly inhibits TLR4 expression in inflammatory cells such as macrophages, thereby reducing secretion of cytokines during peritonitis.

Indexed as

Alum, aluminum potassium sulfateBMDMs, bone marrow–derived macrophagesCytokineHKST, heat-killed Salmonella typhimuriumIL, interleukinip, intraperitoneallyKorean Red Ginseng extractsLB, Luria-BertaniLCCM, L929 cell-conditioned mediumLPS, lipopolysaccharideLys, lysateMSU, monosodium urate crystalNF-kB, nuclear factor kappa-light-chain-enhancer of activated B cellsNLRP3, (NOD)2-like receptor protein 3NOD, nucleotide-binding and oligomerization domainNon, nontreatmentNonsaponin fractionNS, nonsaponin fractionPECs, peritoneal exudate cellsPeritonitisRGE, Korean Red Ginseng extractsSF, saponin fractionSup, supernatantTLR4TLRs, toll-like receptors

Identifiers

PMID30976167
PMCPMC6437451
OpenAlexW2796086789

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.