Evidence map›Paper›PMID 30794635›Full record

ArticlePloS one2019

NAMPT overexpression alleviates alcohol-induced hepatic steatosis in mice.

Xiwen Xiong, Jiahui Yu, Rui Fan, Cuicui Zhang, Lin Xu, Xupeng Sun, Yanmei Huang, Qingzhi Wang, Hai-Bin Ruan, Xinlai Qian

Open access · goldAbstract read
In one paragraph

Article in PloS one, 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, 26 citations in OpenAlex.

  1. Article
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  11. Involvement of eNAMPT/TLR4 inflammatory signaling in progression of non-alcoholic fatty liver disease, steatohepatitis, and fibrosis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  12. Article
  13. Review
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  18. Age-related NADExperimental gerontology · 2020
    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

10 authors at 3 institutions in 2 countries.

Xiwen XiongSchool of Forensic Medicine, Xinxiang Medical University, Xinxiang, Henan, China.ORCID 0000-0001-5802-4994
Jiahui YuSchool of Forensic Medicine, Xinxiang Medical University, Xinxiang, Henan, China.
Rui FanSchool of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, Henan, China.
Cuicui ZhangSchool of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, Henan, China.
Lin XuDepartment of Medical Genetics, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Xupeng SunSchool of Forensic Medicine, Xinxiang Medical University, Xinxiang, Henan, China.
Yanmei HuangSchool of Forensic Medicine, Xinxiang Medical University, Xinxiang, Henan, China.
Qingzhi WangSchool of Forensic Medicine, Xinxiang Medical University, Xinxiang, Henan, China.
Hai-Bin RuanSchool of Forensic Medicine, Xinxiang Medical University, Xinxiang, Henan, China.
Xinlai QianSchool of Forensic Medicine, Xinxiang Medical University, Xinxiang, Henan, China.
Xinxiang Medical University · CNHuazhong University of Science and Technology · CNUniversity of Minnesota Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nicotinamide phosphoribosyltransferase (NAMPT) is a rate-limiting enzyme in mammalian nicotinamide adenine dinucleotide (NAD)+ biosynthesis. Through its NAD+-biosynthetic activity, NAMPT influences the activity of NAD+-dependent enzymes, such as sirtuins. NAMPT is able to modulate processes involved in the pathogenesis of non-alcohol induced fatty liver disease (NAFLD), but the roles NAMPT plays in development of alcoholic liver disease (ALD) still remain unknown. Here, we show that ethanol treatment suppresses the expression of Nampt in hepatocytes. Consistently, chronic ethanol administration also reduces Nampt expression in the mouse liver. We next demonstrate that hepatocytes infected with Ad-NAMPT adenovirus exhibit significantly elevated intracellular NAD+ levels and decreased ethanol-induced triglyceride (TG) accumulation. Similarly, adenovirus-mediated overexpression of NAMPT in mice ameliorates ethanol induced hepatic steatosis. Moreover, we demonstrate that SIRT1 is required to mediate the effects of NAMPT on reduction of hepatic TG accumulation and serum ALT, AST levels in ethanol-fed mice. Our results provide important insights in targeting NAMPT for treating alcoholic fatty liver disease.

Indexed as

AdenoviridaeAnimalsCells, CulturedCytokinesDisease Models, AnimalDown-RegulationEthanolFatty Liver, AlcoholicGene Knockdown TechniquesGenetic TherapyHepatocytesMaleMiceMice, Inbred C57BLMice, KnockoutNADCytokinesEthanolNADNicotinamide Phosphoribosyltransferasenicotinamide phosphoribosyltransferase, mouseRecombinant Fusion ProteinsSirt1 protein, mouseSirt6 protein, mouseSirtuin 1SirtuinsTriglycerides

Identifiers

PMID30794635
PMCPMC6386387
OpenAlexW2917876451

What OpenQuestion holds

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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.