Summary of Study ST001502

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001015. The data can be accessed directly via it's Project DOI: 10.21228/M8H40X This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

Show all samples  |  Perform analysis on untargeted data  
Download mwTab file (text)   |  Download mwTab file(JSON)   |  Download data files (Contains raw data)
Study IDST001502
Study TitleMetabolomics reveals the protective effect of isosteviol sodium against multiple organ injury in septic mice - Lung
Study SummarySepsis is a severe inflammatory disorder that can lead to multiple organ injury. Isosteviol sodium (STV-Na) is a terpenoid derived from stevioside that exerts anti-inflammatory, antioxidant and anticancer activities. However, the influence of STV-Na on sepsis remains unknown. Here, we assessed the potential effects of STV-Na on sepsis and multiple organ injury induced by lipopolysaccharide (LPS). We found that STV-Na increased the survival rate of mice treat with LPS, significantly improved the functions of the heart, lung, liver, and kidney, and reduced the production of inflammatory cytokines. Moreover, Multiorgan metabolomics analysis demonstrated that glutathione metabolism, purine metabolism, glycerophospholipid metabolism and pantothenate and CoA biosynthesis, were significantly altered by STV-Na. This study provides novel insights into the metabolite changes of multiple organ injury in septic mice, which may help characterize the underlying mechanism and provide an improved understanding of the therapeutic effects of STV-Na on sepsis.Mice are randomly assigned to 4 groups in study design. Control: saline + saline Model: saline + LPS; Treatment: STV-Na + LPS; Positive: dexamethasone (Dex) + LPS. Drugs were administered i.p. Six hours after LPS injection, mice were sacrificed. And blood and tissues (heart, lung, liver, spleen and kidney) were subjected to UHPLC-TIMS TOF MS/MS-based metabolomics analyses.
Institute
Guangdong University of Technology
Last NameWang
First NameShanping
AddressNo. 100, Waihuan Xilu, Guangzhou Higher Education Mega Center, Panyu District,
Emailshanpingwang@outlook.com
Phone15521002792
Submit Date2020-09-29
Raw Data AvailableYes
Raw Data File Type(s)d
Analysis Type DetailLC-MS
Release Date2021-03-01
Release Version1
Shanping Wang Shanping Wang
https://dx.doi.org/10.21228/M8H40X
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Factors:

Subject type: Mammal; Subject species: Mus musculus (Factor headings shown in green)

mb_sample_id local_sample_id Treatment
SA126490Ctrl-7Control
SA126491Ctrl-9Control
SA126492Ctrl-6Control
SA126493Ctrl-1Control
SA126494Ctrl-8Control
SA126495Ctrl-5Control
SA126496Ctrl-2Control
SA126497Ctrl-3Control
SA126498Ctrl-4Control
SA126499LPS-8Model
SA126500LPS-9Model
SA126501LPS-12Model
SA126502LPS-7Model
SA126503LPS-10Model
SA126504LPS-11Model
SA126505LPS-6Model
SA126506LPS-1Model
SA126507LPS-3Model
SA126508LPS-2Model
SA126509LPS-4Model
SA126510LPS-5Model
SA126511Dex-1Positive
SA126512Dex-2Positive
SA126513Dex-4Positive
SA126514Dex-3Positive
SA126515Dex-9Positive
SA126516Dex-10Positive
SA126517Dex-5Positive
SA126518Dex-8Positive
SA126519Dex-7Positive
SA126520Dex-6Positive
SA126521STV-7Treatment
SA126522STV-2Treatment
SA126523STV-1Treatment
SA126524STV-3Treatment
SA126525STV-4Treatment
SA126526STV-5Treatment
SA126527STV-6Treatment
Showing results 1 to 38 of 38
  logo