Evidence map›Paper›PMID 28779013›Full record

ArticleBioscience reports2017

Ginsenoside Rg3 attenuates sepsis-induced injury and mitochondrial dysfunction in liver via AMPK-mediated autophagy flux.

Wei Xing, Lei Yang, Yue Peng, Qianlu Wang, Min Gao, Mingshi Yang, Xianzhong Xiao

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

45 citing papers in PubMed, 69 citations in OpenAlex.

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  14. Targeting AMP-activated protein kinase in sepsis.Frontiers in endocrinology · 2024
    Review
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  16. Review
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  18. Role of Mitophagy in Regulating Intestinal Oxidative Damage.Antioxidants (Basel, Switzerland) · 2023
    Review
  19. 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

7 authors at 3 institutions in 1 country.

Wei XingDepartment of Intensive Medicine, Third Xiangya Hospital, Central South University, Changsha 410013, P.R. China.
Lei YangDepartment of Pharmacy, First Affiliated Hospital of Hunan University of Traditional Chinese Medicine, Changsha 410013, P.R. China.
Yue PengDepartment of Intensive Medicine, Third Xiangya Hospital, Central South University, Changsha 410013, P.R. China.
Qianlu WangDepartment of Intensive Medicine, Third Xiangya Hospital, Central South University, Changsha 410013, P.R. China.
Min GaoDepartment of Intensive Medicine, Third Xiangya Hospital, Central South University, Changsha 410013, P.R. China.
Mingshi YangDepartment of Intensive Medicine, Third Xiangya Hospital, Central South University, Changsha 410013, P.R. China.
Xianzhong XiaoDepartment of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha 410078, Hunan Province, P.R. China xiaoxianzhong@csu.edu.cn.
Central South University · CNThird Xiangya Hospital · CNFirst Affiliated Hospital of Hunan University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis-led mitochondrial dysfunction has become a critical pathophysiological procedure in sepsis. Since ginsenosides have been applied in the treatment of mitochondrial dysfunction, ginsenoside Rg3 was employed to study its effects on the mitochondrial dysfunction induced by sepsis. The apoptosis rate, oxygen consumption rate (OCR), reactive oxygen species (ROS), antioxidant glutathione (GSH) pools, and mitochondrial transmembrane potential (MTP) were determined in LPS-induced sepsis hepatocytes treated with different concentrations of Rg3. Then, the protein expression levels of mitochondrial biogenesis related transcription factors, autophagy-related proteins, and AMP-activated protein kinase (AMPK) signal pathway related proteins were determined by Western blotting in both

Indexed as

AMP-Activated Protein KinasesAnimalsAutophagyChemical and Drug Induced Liver InjuryGinsenosidesHumansLipopolysaccharidesMaleMiceMitochondrial DiseasesMitochondria, LiverReactive Oxygen SpeciesSepsisAMP-Activated Protein Kinasesginsenoside Rg3GinsenosidesLipopolysaccharidesReactive Oxygen SpeciesAutophagyLiver injuryMitochondrial dysfunctionRg3Sepsis

Identifiers

PMID28779013
PMCPMC5577177
OpenAlexW2745198396

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.