Summary of Study ST001499

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.

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Study IDST001499
Study TitleMetabolomics reveals the protective effect of isosteviol sodium against multiple organ injury in septic mice - Heart
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

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Factors:

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

mb_sample_id local_sample_id Groups
SA126358Ctrl-8Control
SA126359Ctrl-1Control
SA126360Ctrl-7Control
SA126361Ctrl-6Control
SA126362Ctrl-2Control
SA126363Ctrl-4Control
SA126364Ctrl-3Control
SA126365Ctrl-5Control
SA126366LPS-7Model
SA126367LPS-8Model
SA126368LPS-6Model
SA126369LPS-5Model
SA126370LPS-1Model
SA126371LPS-3Model
SA126372LPS-2Model
SA126373LPS-4Model
SA126374Dex-4Positive
SA126375Dex-3Positive
SA126376Dex-1Positive
SA126377Dex-5Positive
SA126378Dex-8Positive
SA126379Dex-9Positive
SA126380Dex-2Positive
SA126381Dex-7Positive
SA126382Dex-6Positive
SA126383STV-2Treatment
SA126384STV-4Treatment
SA126385STV-3Treatment
SA126386STV-1Treatment
SA126387STV-5Treatment
SA126388STV-6Treatment
SA126389STV-8Treatment
SA126390STV-7Treatment
SA126391STV-9Treatment
Showing results 1 to 34 of 34
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