Effect of molecular hydrogen treatment on Sepsis‐Associated encephalopathy in mice based on gut microbiota. (5th December 2022)
- Record Type:
- Journal Article
- Title:
- Effect of molecular hydrogen treatment on Sepsis‐Associated encephalopathy in mice based on gut microbiota. (5th December 2022)
- Main Title:
- Effect of molecular hydrogen treatment on Sepsis‐Associated encephalopathy in mice based on gut microbiota
- Authors:
- Han, Qingqing
Bai, Yuanyuan
Zhou, Chunjing
Dong, Beibei
Li, Yingning
Luo, Ning
Chen, Hongguang
Yu, Yonghao - Abstract:
- Abstract: Introduction: In our experiments, male wild‐type mice were randomly divided into four groups: the sham, SAE, SAE + 2% hydrogen gas inhalation (H2 ), and SAE + hydrogen‐rich water (HW) groups. The feces of the mice were collected for 16 S rDNA analysis 24 h after the models were established, and the serum and brain tissue of the mice were collected for nontargeted metabolomics analysis. Aim: Destruction of the intestinal microbiota is a risk factor for sepsis and subsequent organ dysfunction, and up to 70% of severely ill patients with sepsis exhibit varying degrees of sepsis‐associated encephalopathy (SAE). The pathogenesis of SAE remains unclear. We aimed to explore the changes in gut microbiota in SAE and the regulatory mechanism of molecular hydrogen. Results: Molecular hydrogen treatment significantly improved the functional outcome of SAE and downregulated inflammatory reactions in both the brain and the gut. In addition, molecular hydrogen treatment improved gut microbiota dysbiosis and partially amended metabolic disorder after SAE. Conclusions: Molecular hydrogen treatment promotes functional outcomes after SAE in mice, which may be attributable to increasing beneficial bacteria, repressing harmful bacteria, and metabolic disorder, and reducing inflammation. Abstract : Molecular hydrogen treatment can significantly improve the gut microbiota and metabolites and reduce the inflammatory reaction and cognitive dysfunction after SAE. This study provides a basisAbstract: Introduction: In our experiments, male wild‐type mice were randomly divided into four groups: the sham, SAE, SAE + 2% hydrogen gas inhalation (H2 ), and SAE + hydrogen‐rich water (HW) groups. The feces of the mice were collected for 16 S rDNA analysis 24 h after the models were established, and the serum and brain tissue of the mice were collected for nontargeted metabolomics analysis. Aim: Destruction of the intestinal microbiota is a risk factor for sepsis and subsequent organ dysfunction, and up to 70% of severely ill patients with sepsis exhibit varying degrees of sepsis‐associated encephalopathy (SAE). The pathogenesis of SAE remains unclear. We aimed to explore the changes in gut microbiota in SAE and the regulatory mechanism of molecular hydrogen. Results: Molecular hydrogen treatment significantly improved the functional outcome of SAE and downregulated inflammatory reactions in both the brain and the gut. In addition, molecular hydrogen treatment improved gut microbiota dysbiosis and partially amended metabolic disorder after SAE. Conclusions: Molecular hydrogen treatment promotes functional outcomes after SAE in mice, which may be attributable to increasing beneficial bacteria, repressing harmful bacteria, and metabolic disorder, and reducing inflammation. Abstract : Molecular hydrogen treatment can significantly improve the gut microbiota and metabolites and reduce the inflammatory reaction and cognitive dysfunction after SAE. This study provides a basis for the pathogenesis and treatment of SAE. … (more)
- Is Part Of:
- CNS neuroscience & therapeutics. Volume 29:Number 2(2023)
- Journal:
- CNS neuroscience & therapeutics
- Issue:
- Volume 29:Number 2(2023)
- Issue Display:
- Volume 29, Issue 2 (2023)
- Year:
- 2023
- Volume:
- 29
- Issue:
- 2
- Issue Sort Value:
- 2023-0029-0002-0000
- Page Start:
- 633
- Page End:
- 645
- Publication Date:
- 2022-12-05
- Subjects:
- gut microbiota -- hydrogen gas (H2) -- hydrogen‐rich water (HW) -- molecular hydrogen treatment -- sepsis‐associated encephalopathy (SAE)
Neuropharmacology -- Periodicals
Central nervous system -- Diseases -- Effect of drugs on -- Periodicals
612.8 - Journal URLs:
- http://www.blackwell-synergy.com/loi/cnsnt ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/cns.14043 ↗
- Languages:
- English
- ISSNs:
- 1755-5930
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9830.140000
British Library DSC - BLDSS-3PM
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