Evidence map›Paper›PMID 35003518›Full record

ArticleOxidative medicine and cellular longevity2021

Pretreatment with 6-Gingerol Ameliorates Sepsis-Induced Immune Dysfunction by Regulating the Cytokine Balance and Reducing Lymphocyte Apoptosis.

Seong-A Ju, Quang-Tam Nguyen, Thu-Ha T Nguyen, Jae-Hee Suh, Won G An, Zak Callaway, Yeonsoo Joe, Hun Taeg Chung, Byung-Sam Kim

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Seong-A JuSchool of Biological Sciences, University of Ulsan, Ulsan 44610, Republic of Korea.
Quang-Tam NguyenSchool of Biological Sciences, University of Ulsan, Ulsan 44610, Republic of Korea.
Thu-Ha T NguyenSchool of Biological Sciences, University of Ulsan, Ulsan 44610, Republic of Korea.
Jae-Hee SuhDepartment of Pathology, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Republic of Korea.
Won G AnDivision of Pharmacology, School of Korean Medicine, Pusan National University, Yangsan 50612, Republic of Korea.
Zak CallawaySchool of Biological Sciences, University of Ulsan, Ulsan 44610, Republic of Korea.
Yeonsoo JoeSchool of Biological Sciences, University of Ulsan, Ulsan 44610, Republic of Korea.
Hun Taeg ChungSchool of Biological Sciences, University of Ulsan, Ulsan 44610, Republic of Korea.ORCID https://orcid.org/0000-0003-4802-7467
Byung-Sam KimSchool of Biological Sciences, University of Ulsan, Ulsan 44610, Republic of Korea.ORCID https://orcid.org/0000-0002-5176-0881
University of Ulsan · KRPusan National University · KRUlsan College · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis is characterized by an initial net hyperinflammatory response, followed by a period of immunosuppression, termed immunoparalysis. During this immunosuppressive phase, patients may have difficulty eradicating invading pathogens and are susceptible to life-threatening secondary hospital-acquired infections. Due to progress in antimicrobial treatment and supportive care, most patients survive early sepsis. Mortality is more frequently attributed to subsequent secondary nosocomial infections and multiorgan system failure. 6-Gingerol is the major pharmacologically active component of ginger. Although it is known to exhibit a variety of biological activities, including anti-inflammation and antioxidation, the role of 6-gingerol in sepsis-induced immune dysfunction remains elusive. Thus, we investigated whether 6-gingerol improves septic host response to infections during sepsis. 6-Gingerol-treated mice showed significantly lower mortality in polymicrobial sepsis induced by cecal ligation and puncture LPS via enhanced bacterial clearance in the peritoneum, blood, and organs (liver, spleen, and kidney) and inhibited the production of TNF-

Indexed as

AnimalsApoptosisCatecholsCytokinesFatty AlcoholsHumansImmune System DiseasesLymphocytesMaleMiceSepsisCatecholsCytokinesFatty Alcoholsgingerol

Identifiers

PMID35003518
PMCPMC8731291
OpenAlexW4200530098

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.