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Atractylone Alleviates Ethanol-Induced Gastric Ulcer in Rat with Altered Gut Microbiota and Metabolites
by
Wang, Yang
, Wang, Bing
, He, Ning
, Zhang, Tong
, Du, Yaoyao
, Li, Ling
in
Acetaldehyde
/ Alcohol
/ Alcohol, Denatured
/ Animal models
/ Antioxidants
/ atractylone
/ Bile acids
/ Cytokines
/ Digestive system
/ Discriminant analysis
/ Ethanol
/ Fatty acids
/ Gastric mucosa
/ gastric ulcer
/ Gastrointestinal tract
/ Gut microbiota
/ Helicobacter pylori
/ Inflammation
/ Intestinal microflora
/ Metabolites
/ Metabolomics
/ Microbiota
/ Microbiota (Symbiotic organisms)
/ Neutrophils
/ Original Research
/ Oxidative stress
/ Phenotypes
/ RNA
/ rRNA 16S
/ Stomach ulcer
/ Superoxide
/ Superoxide dismutase
/ Traditional Chinese medicine
/ Tumor necrosis factor-TNF
/ Ulcers
/ Zebrafish
2022
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Atractylone Alleviates Ethanol-Induced Gastric Ulcer in Rat with Altered Gut Microbiota and Metabolites
by
Wang, Yang
, Wang, Bing
, He, Ning
, Zhang, Tong
, Du, Yaoyao
, Li, Ling
in
Acetaldehyde
/ Alcohol
/ Alcohol, Denatured
/ Animal models
/ Antioxidants
/ atractylone
/ Bile acids
/ Cytokines
/ Digestive system
/ Discriminant analysis
/ Ethanol
/ Fatty acids
/ Gastric mucosa
/ gastric ulcer
/ Gastrointestinal tract
/ Gut microbiota
/ Helicobacter pylori
/ Inflammation
/ Intestinal microflora
/ Metabolites
/ Metabolomics
/ Microbiota
/ Microbiota (Symbiotic organisms)
/ Neutrophils
/ Original Research
/ Oxidative stress
/ Phenotypes
/ RNA
/ rRNA 16S
/ Stomach ulcer
/ Superoxide
/ Superoxide dismutase
/ Traditional Chinese medicine
/ Tumor necrosis factor-TNF
/ Ulcers
/ Zebrafish
2022
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Atractylone Alleviates Ethanol-Induced Gastric Ulcer in Rat with Altered Gut Microbiota and Metabolites
by
Wang, Yang
, Wang, Bing
, He, Ning
, Zhang, Tong
, Du, Yaoyao
, Li, Ling
in
Acetaldehyde
/ Alcohol
/ Alcohol, Denatured
/ Animal models
/ Antioxidants
/ atractylone
/ Bile acids
/ Cytokines
/ Digestive system
/ Discriminant analysis
/ Ethanol
/ Fatty acids
/ Gastric mucosa
/ gastric ulcer
/ Gastrointestinal tract
/ Gut microbiota
/ Helicobacter pylori
/ Inflammation
/ Intestinal microflora
/ Metabolites
/ Metabolomics
/ Microbiota
/ Microbiota (Symbiotic organisms)
/ Neutrophils
/ Original Research
/ Oxidative stress
/ Phenotypes
/ RNA
/ rRNA 16S
/ Stomach ulcer
/ Superoxide
/ Superoxide dismutase
/ Traditional Chinese medicine
/ Tumor necrosis factor-TNF
/ Ulcers
/ Zebrafish
2022
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Atractylone Alleviates Ethanol-Induced Gastric Ulcer in Rat with Altered Gut Microbiota and Metabolites
Journal Article
Atractylone Alleviates Ethanol-Induced Gastric Ulcer in Rat with Altered Gut Microbiota and Metabolites
2022
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Overview
Gastric ulcer (GU) is the most common multifactor gastrointestinal disorder affecting millions of people worldwide. There is evidence that gut microbiota is closely related to the development of GU. Atractylone (ATR) has been reported to possess potential biological activities, but research on ATR alleviating GU injury is unprecedented.
(
)-induced GU model in zebrafish and ethanol-induced acute GU model in rat were established to evaluate the anti-inflammatory and ulcer inhibitory effects of ATR. Then, 16S rRNA sequencing and metabolomics analysis were performed to investigate the effect of ATR on the microbiota and metabolites in rat feces and their correlation.
Therapeutically, ATR inhibited
-induced gastric mucosal injury in zebrafish. In the ulceration model of rat, ATR mitigated the gastric lesions damage caused by ethanol, decreased the ulcer area, and reduced the production of inflammatory factors. Additionally, ATR alleviated the gastric oxidative stress injury by increasing the activity of superoxide dismutase (SOD) and decreasing the level of malondialdehyde (MDA). Furthermore, ATR played a positive role in relieving ulcer through reshaping gut microbiota composition including
and
and regulating the levels of metabolites including amino acids, short-chain fatty acids (SCFAs), and bile acids.
Our work sheded light on the mechanism of ATR treating GU from the perspective of the gut microbiota and explored the correlation between gut microbiota, metabolites, and host phenotype.
Publisher
Dove Medical Press Limited,Taylor & Francis Ltd,Dove,Dove Medical Press
Subject
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