Evidence map›Paper›PMID 39182019›Full record

ArticleGenes & nutrition2024

Protective effects of Nogo-B deficiency in NAFLD mice and its multiomics analysis of gut microbiology and metabolism.

Xu Dong, Yu-Ting Xiong, Tingting He, Congyang Zheng, Junjie Li, Yingjie Zhuang, Yingjie Xu, Ye Xiu, Zhixin Wu, Xiaomei Zhao and 3 more

Abstract read
In one paragraph

Article in Genes & nutrition, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Protective Effects ofJournal of microbiology and biotechnology · 2026
    Article
  2. Article
  3. Article
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

13 authors.

Xu Dong *Medical School of Chinese PLA, Beijing, China.
Yu-Ting Xiong *307 Clinical Medical College of PLA, Anhui Medical University, Beijing, China.
Tingting He *Department of Hepatology Medicine of Traditional Chinese Medicine, The Fifth Medical Center, Chinese PLA General Hospital, Beijing, China.
Congyang ZhengMedical School of Chinese PLA, Beijing, China.
Junjie LiDepartment of Hepatology, The Fifth Medical Center, Chinese PLA General Hospital, Beijing, China.
Yingjie ZhuangDepartment of Gastroenterology, The Second Medical Center, Chinese PLA General Hospital, Beijing, China.
Yingjie XuDepartment of Hepatology, The Fifth Medical Center, Chinese PLA General Hospital, Beijing, China.
Ye XiuDepartment of Hepatology, The Fifth Medical Center, Chinese PLA General Hospital, Beijing, China.
Zhixin WuDepartment of Hepatology, The Fifth Medical Center, Chinese PLA General Hospital, Beijing, China.
Xiaomei ZhaoDepartment of Hepatology, The Fifth Medical Center, Chinese PLA General Hospital, Beijing, China.
Xiaohe XiaoDepartment of Hepatology, The Fifth Medical Center, Chinese PLA General Hospital, Beijing, China. pharmacy_302@126.com.
Zhaofang BaiDepartment of Hepatology, The Fifth Medical Center, Chinese PLA General Hospital, Beijing, China. baizf2008@hotmail.com.
Lili GaoMedical School of Chinese PLA, Beijing, China. gll301818@163.com.

Funding

Foundation for lnnovative Research Groups of the National Natural ScienceFoundation of China 81721002Innovation Team and Talents Cultivation Program of National Administration of Traditional Chinese Medicine ZYYCXTD-C-202005
6 · The paper itself

Abstract

backgroundNonalcoholic fatty liver disease (NAFLD) is a prevalent chronic liver ailment that can lead to serious conditions such as cirrhosis and hepatocellular carcinoma. Hepatic Nogo-B regulates glucose and lipid metabolism, and its inhibition has been shown to be protective against metabolic syndrome. Increasing evidence suggests that imbalances in the gut microbiota (GM) and lipid metabolism disorders are significant contributors to NAFLD progression. Nevertheless, it is not yet known whether Nogo-B can affect NAFLD by influencing the gut microbiota and metabolites. Hence, the aim of the present study was to characterize this process and explore its possible underlying mechanisms.

methodsA NAFLD model was constructed by administering a high-fat diet (HFD) to Nogo-B

resultsNogo-B deficiency attenuated the effects of the HFD, including weight gain, liver weight gain, impaired glucose tolerance, hepatic steatosis, elevated serum lipid biochemicals levels, and liver function. Nogo-B deficiency suppressed M1 polarization and promoted M2 polarization, thus inhibiting inflammatory responses. Furthermore, Nogo-B

conclusionNogo-B deficiency delayed NAFLD progression, as demonstrated by reduced hepatocellular lipid accumulation, attenuated inflammation and liver injury, and ameliorated gut microbiota dysbiosis and metabolic disorders. Importantly, Odoribacter was strongly positively correlated with ALB and taurodeoxycholic acid, suggesting that it played a considerable role in the influence of Nogo-B on the progression of NAFLD, a specific feature of NAFLD in Nogo-B

Indexed as

Gut microbiotaMetabonomicsNAFLDNogo-B

Identifiers

PMID39182019
PMCPMC11344411

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Registered trials

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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.