Summary of Study ST002813

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 PR001760. The data can be accessed directly via it's Project DOI: 10.21228/M86T5X 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 IDST002813
Study TitleEffects of acute cold exposure on mouse metabolome
Study SummaryCold-induced thermogenesis is widely studied as a potential avenue to treat obesity, but a thorough understanding of the metabolic changes driving thermogenesis is lacking. We analyzed mouse plasma and tissue samples from fasted mice housed at room temperature or acutely exposed to 4°C. First, C57BL/6 mice (n=41) were divided into 2 groups (n=20-21 per group) and underwent surgery to implant an indwelling arterial catheter. Mice originally housed at room temperature were housed without food for 6 hours at room temperature or 4°C, after which blood was collected from the arterial catheter and centrifuged, and plasma was collected for metabolomic analyses. Second, C57BL/6 mice (n=12) were divided into 2 groups (n=6 per group) and housed without food for 6 hours at room temperature or 4°C. Mice were euthanized, and tissues (brown adipose tissue, heart, liver, quadricepts muscle, diaphragm, and gonadal-white adipose tissue) were collected, freeze-clamped in liquid nitrogen, and used for metabolomic analyses. Overall our data detail a coordinated and broad metabolic response governing the thermogenic response to acute cold exposure in mice.
Institute
University of Pennsylvania
DepartmentMedicine
LaboratoryArany Lab
Last NameBornstein
First NameMarc
Address3400 Civic Center Blvd (Smilow 11-187)
Emailmarc.bornstein@pennmedicine.upenn.edu
Phone7742796684
Submit Date2023-08-09
Num Groups4
Total Subjects53
Num Males53
Raw Data AvailableYes
Raw Data File Type(s)mzXML
Analysis Type DetailLC-MS
Release Date2023-10-05
Release Version1
Marc Bornstein Marc Bornstein
https://dx.doi.org/10.21228/M86T5X
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN004575 AN004576 AN004577 AN004578
Analysis type MS MS MS MS
Chromatography type HILIC HILIC Reversed phase Reversed phase
Chromatography system Thermo Vanquish Thermo Vanquish Thermo Vanquish Thermo Vanquish
Column Waters XBridge BEH Amide (150 x 2.1mm,2.5um) Waters XBridge BEH Amide (150 x 2.1mm,2.5um) Agilent InfinityLab Poroshell 120 EC-C8 (150 x 2.1mm,2.7um) Agilent InfinityLab Poroshell 120 EC-C8 (150 x 2.1mm,2.7um)
MS Type ESI ESI ESI ESI
MS instrument type Orbitrap Orbitrap Orbitrap Orbitrap
MS instrument name Thermo Q Exactive Plus Orbitrap Thermo Q Exactive Plus Orbitrap Thermo Q Exactive Plus Orbitrap Thermo Q Exactive Plus Orbitrap
Ion Mode POSITIVE NEGATIVE POSITIVE NEGATIVE
Units Intensity Intensity Intensity intensity

Chromatography:

Chromatography ID:CH003439
Chromatography Summary:Chromatography for hydrophilic compounds
Instrument Name:Thermo Vanquish
Column Name:Waters XBridge BEH Amide (150 x 2.1mm,2.5um)
Column Temperature:35
Flow Gradient:0 min, 85% B; 2 min, 85% B; 3 min, 80% B; 5 min, 80% B; 6 min, 75% B; 7 min, 75% B; 8 min, 70% B; 9 min, 70% B; 10 min, 50% B; 12 min, 50% B; 13 min, 25% B; 16 min, 25% B; 18 min, 0% B; 23 min, 0% B; 24 min, 85% B; and 30 min, 85% B.
Flow Rate:150 uL/min
Solvent A:95% water/5% acetonitrile; 20 mM ammonium acetate; mM ammonium hydroxide, pH 9.45)
Solvent B:100% acetonitrile
Chromatography Type:HILIC
  
Chromatography ID:CH003440
Chromatography Summary:Chromatography for lipids
Instrument Name:Thermo Vanquish
Column Name:Agilent InfinityLab Poroshell 120 EC-C8 (150 x 2.1mm,2.7um)
Column Temperature:35
Flow Gradient:0 minutes, 25% B; 2 minutes, 25% B; 4 minutes, 65% B; 16 minutes, 100% B; 20 minutes, 100% B; 21 minutes, 25% B; 27 minutes, 25% B
Flow Rate:150 uL/min
Solvent A:90% water/10% methanol; 1mM ammonium acetate ; 0.2% acetic acid
Solvent B:2% methanol/98% isopropano; 1 mM ammonium acetate; 0.2% acetic acid
Chromatography Type:Reversed phase
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