Evidence map›Paper›PMID 31412594›Full record

ArticleNutrients2019

Greater Efficacy of Black Ginseng (CJ EnerG) over Red Ginseng against Lethal Influenza A Virus Infection.

Eun-Ha Kim, Son-Woo Kim, Su-Jin Park, Semi Kim, Kwang-Min Yu, Seong Gyu Kim, Seung Hun Lee, Yong-Ki Seo, Nam-Hoon Cho, Kimoon Kang and 2 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Antiviral Potential of the GenusJournal of ginseng research · 2023
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. 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

12 authors at 2 institutions in 1 country.

Eun-Ha KimCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Korea.
Son-Woo KimThe Institutes of Food, CJ CheilJedang, Suwon 16495, Korea.
Su-Jin ParkCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Korea.
Semi KimCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Korea.
Kwang-Min YuCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Korea.
Seong Gyu KimID Bio Corporation, Cheongju 28370, Korea.
Seung Hun LeeCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Korea.
Yong-Ki SeoThe Institutes of Food, CJ CheilJedang, Suwon 16495, Korea.
Nam-Hoon ChoThe Institutes of Food, CJ CheilJedang, Suwon 16495, Korea.
Kimoon KangThe Institutes of Food, CJ CheilJedang, Suwon 16495, Korea.
Do Y SoungThe Institutes of Food, CJ CheilJedang, Suwon 16495, Korea. doyu.soung@cj.net.
Young-Ki ChoiCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Korea. choiki55@chungbuk.ac.kr.
CJ CheilJedang (South Korea) · KRChungbuk National University · KR

Funding

CJ CheilJedang Corporation NANational Research Foundation of Korea NRF-2018M3A9H4056536
6 · The paper itself

Abstract

Black ginseng (BG, CJ EnerG), prepared via nine repeated cycles of steaming and drying of fresh ginseng, contains more accessible acid polysaccharides and smaller and less polar ginsenosides than red ginseng (RG) processed only once. Because RG exhibits the ability to increase host protection against viral respiratory infections, we investigated the antiviral effects of BG. Mice were orally administered either BG or RG extract at 10 mg/kg bw daily for two weeks. Mice were then infected with a A(H1N1) pdm09 (A/California/04/2009) virus and fed extracts for an additional week. Untreated, infected mice were assigned to either the negative control, without treatments, or the positive control, treated with Tamiflu. Infected mice were monitored for 14 days to determine the survival rate. Lung tissues were evaluated for virus titer and by histological analyses. Cytokine levels were measured in bronchoalveolar lavage fluid. Mice treated with BG displayed a 100% survival rate against infection, while mice treated with RG had a 50% survival rate. Further, mice treated with BG had fewer accumulated inflammatory cells in bronchioles following viral infection than did mice treated with RG. BG also enhanced the levels of GM-CSF and IL-10 during the early and late stages of infection, respectively, compared to RG. Thus, BG may be useful as an alternative antiviral adjuvant to modulate immune responses to influenza A virus.

Indexed as

PanaxAnimalsAntiviral AgentsCytokinesDisease Models, AnimalFemaleHost-Pathogen InteractionsInfluenza A Virus, H1N1 SubtypeLungMice, Inbred BALB COrthomyxoviridae InfectionsPlant ExtractsRespiratory Tract InfectionsViral LoadAntiviral AgentsCytokinesPlant Extractsantiviralblack ginsengcytokinesinfluenza A virusoral administration

Identifiers

PMID31412594
PMCPMC6723933
OpenAlexW2967554560

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.