Evidence map›Paper›PMID 38329114›Full record

ArticleRedox report : communications in free radical research2024

Glutamine sustains energy metabolism and alleviates liver injury in burn sepsis by promoting the assembly of mitochondrial HSP60-HSP10 complex via SIRT4 dependent protein deacetylation.

Yongjun Yang, Qian Chen, Shijun Fan, Yongling Lu, Qianyin Huang, Xin Liu, Xi Peng

Open access · goldAbstract read
In one paragraph

Article in Redox report : communications in free radical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

21 citing papers in PubMed, 22 citations in OpenAlex.

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  19. Molecular Chaperonin HSP60: Current Understanding and Future Prospects.International journal of molecular sciences · 2024
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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 2 institutions in 1 country.

Yongjun YangClinical Medical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, People's Republic of China.
Qian ChenClinical Medical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, People's Republic of China.
Shijun FanClinical Medical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, People's Republic of China.
Yongling LuClinical Medical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, People's Republic of China.
Qianyin HuangClinical Medical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, People's Republic of China.
Xin LiuClinical Medical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, People's Republic of China.
Xi PengClinical Medical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, People's Republic of China.
Southwest Hospital · CNArmy Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Burns and burn sepsis, characterized by persistent and profound hypercatabolism, cause energy metabolism dysfunction that worsens organ injury and systemic disorders. Glutamine (Gln) is a key nutrient that remarkably replenishes energy metabolism in burn and sepsis patients, but its exact roles beyond substrate supply is unclear. In this study, we demonstrated that Gln alleviated liver injury by sustaining energy supply and restoring redox balance. Meanwhile, Gln also rescued the dysfunctional mitochondrial electron transport chain (ETC) complexes, improved ATP production, reduced oxidative stress, and protected hepatocytes from burn sepsis injury. Mechanistically, we revealed that Gln could activate SIRT4 by upregulating its protein synthesis and increasing the level of Nicotinamide adenine dinucleotide (NAD

Indexed as

BurnsSepsisSirtuinsAdenosine TriphosphateEnergy MetabolismGlutamineHumansLiverMitochondrial ProteinsAdenosine TriphosphateGlutamineMitochondrial ProteinsSIRT4 protein, humanSirtuinsburn sepsisenergy metabolismGlutamineHSP60-HSP10 assemblyliver injurymitochondrial electron transport chainreactive oxygen speciesSirtuin 4

Identifiers

PMID38329114
PMCPMC10854458
OpenAlexW4391653561

What Socratic 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 Socratic graph.