Evidence map›Paper›PMID 35784533›Full record

ArticleFrontiers in endocrinology2022

Fufang Zhenzhu Tiaozhi Capsule Prevents Intestinal Inflammation and Barrier Disruption in Mice With Non-Alcoholic Steatohepatitis.

Tian Lan, Tonghao Xu, Yanfang Fu, Shuo Jiang, Xiaolin Liang, Ze Yu, Linyu Pan, Xianglu Rong, Jiao Guo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Repairing gut barrier by traditional Chinese medicine: roles of gut microbiota.Frontiers in cellular and infection microbiology · 2024
    Review
  5. 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

9 authors at 2 institutions in 1 country.

Tian LanInstitute of Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Tonghao XuInstitute of Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Yanfang FuInstitute of Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Shuo JiangInstitute of Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Xiaolin LiangInstitute of Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Ze YuInstitute of Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Linyu PanInstitute of Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Xianglu RongInstitute of Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Jiao GuoInstitute of Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Ministry of Education of the People's Republic of China · CNGuangdong Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonalcoholic steatohepatitis (NASH) has become a major cause of liver transplantation and liver-associated death. Targeting the gut-liver axis is a potential therapy for NASH. The Fufang Zhenzhu Tiaozhi (FTZ) capsule, a traditional Chinese medicine commonly used in clinical practice, has recently emerged as a promising drug candidate for metabolic diseases such as NASH. The present study aimed to investigate whether FTZ exerts an anti-NASH effect by targeting the gut-liver axis. Mice were fed with a high-fat diet (HFD) for 20 weeks to induce NASH. HFD-fed mice were daily intragastrically administrated with FTZ at 10 weeks after tbe initiation of HFD feeding. The mRNA levels of genes associated with the intestinal tight junction, lipid metabolism, and inflammation were determined by the q-PCR assay. Hepatic pathology was evaluated by H&E staining. The gut microbiota was analyzed by 16S rRNA gene sequencing. FTZ attenuated HFD-induced obesity, insulin resistance, and hepatic steatosis in mice. FTZ treatment decreased the elevated levels of serum aminotransferases and liver triglyceride in NASH mice. Furthermore, FTZ treatment reduced hepatic inflammatory cell infiltration and fibrosis in mice. In addition, FTZ attenuated the intestinal inflammatory response and improved intestinal barrier function. Mechanistically, FTZ-treated mice showed a different gut microbiota composition compared with that in HFD-fed mice. Finally, we identified eight differential metabolites that may contribute to the improvement of NASH with FTZ treatment. In summary, FTZ ameliorates NASH by inhibiting gut inflammation, improving intestinal barrier function, and modulating intestinal microbiota composition.

Indexed as

Non-alcoholic Fatty Liver DiseaseAnimalsDiet, High-FatInflammationMiceMice, Inbred C57BLRNA, Ribosomal, 16SRNA, Ribosomal, 16Sgut–liver axisintestinal barrierintestinal microbiotaNASHtraditional Chinese medicine

Identifiers

PMID35784533
PMCPMC9243428
OpenAlexW4282977611

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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.