Summary of Study ST002186

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 PR001393. The data can be accessed directly via it's Project DOI: 10.21228/M8NT4K 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 IDST002186
Study TitleAn early-life microbiota metabolite protects against obesity via intestinal PPAR-gamma
Study Typeuntargeted metabolomics analysis
Study SummaryThe mechanisms by which the early-life microbiota protects against environmental factors that promote childhood obesity remain largely unknown. Using a mouse model in which young mice are simultaneously exposed to antibiotics and a high-fat diet, we show that Lactobacillus species, predominant members of the small intestine microbiota, regulate intestinal epithelial cells (IECs) to limit diet-induced obesity during early-life. A Lactobacillus-derived metabolite, phenyllactic acid (PLA), protected against metabolic dysfunction caused by early-life exposure to antibiotics and a high-fat diet by increasing the abundance of peroxisome proliferator activated receptor gamma (PPAR-gamma) in the small intestine IECs. Therefore, PLA is a microbiota-derived metabolite that activates protective pathways in the small intestine epithelium to regulate fat absorption and prevent obesity during early life.
Institute
Vanderbilt University
DepartmentChemistry
LaboratoryCenter for Innovative Technology
Last NameCodreanu
First NameSimona Gabriella
Address1234 Stevenson Center Lane
EmailSIMONA.CODREANU@VANDERBILT.EDU
Phone6158758422
Submit Date2022-06-03
Num Groups4
Total Subjects20
Num Males20
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo)
Analysis Type DetailLC-MS
Release Date2023-06-06
Release Version1
Simona Gabriella Codreanu Simona Gabriella Codreanu
https://dx.doi.org/10.21228/M8NT4K
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN003580
Analysis type MS
Chromatography type Reversed phase
Chromatography system Thermo Vanquish
Column Thermo Hypersil Gold (100 x 2. mm,1.9um)
MS Type ESI
MS instrument type QTRAP
MS instrument name Thermo Q Exactive HF hybrid Orbitrap
Ion Mode NEGATIVE
Units time_m/z

Chromatography:

Chromatography ID:CH002647
Chromatography Summary:Prepared samples were analyzed by RPLC-HRMS/MS in the Vanderbilt Center for Innovative Technology (CIT) using a modified version of a reversed phase chromatography negative ionization method. Metabolites were separated on a Thermo Fisher Scientific (Waltham, MA) Hypersil Gold C18 column (100 x 2.1 mm, 1.9 μm particle size) using water/acetonitrile gradient with formic acid (0.1%) added to both mobile phases.
Instrument Name:Thermo Vanquish
Column Name:Thermo Hypersil Gold (100 x 2. mm,1.9um)
Column Temperature:40
Flow Rate:0.25 mL/min
Solvent A:100% water; 0.1% formic acid
Solvent B:80% acetonitrile/20% water; 0.1% formic acid
Chromatography Type:Reversed phase
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