Summary of Study ST001366

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 PR000934. The data can be accessed directly via it's Project DOI: 10.21228/M8ZH61 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 IDST001366
Study TitleMalnutrition and Liver Metabolomics
Study SummaryRP-UPLC-FTMS (+/- ion detection) were conducted on hippocampi from healthy (CON) and malnourished (MAL) mice, and MAL-BG (malnutrition plus E.coli/Bacteroidales exposure) mice.
Institute
University of British Columbia
DepartmentMicrobiology and Immunology
LaboratoryB. Brett Finlay
Last NameBauer
First NameKylynda
AddressMichael Smith Laboratories, #301 – 2185 East Mall, University of British Columbia Vancouver, British Columbia Canada, V6T 1Z4
Emailkcbauer@msl.ubc.ca
Phone(604) 822-2210
Submit Date2020-04-24
Num Groups3
Total Subjects15
Num Females15
Raw Data AvailableYes
Analysis Type DetailLC-MS
Release Date2021-06-30
Release Version1
Kylynda Bauer Kylynda Bauer
https://dx.doi.org/10.21228/M8ZH61
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR000934
Project DOI:doi: 10.21228/M8ZH61
Project Title:Malnutrition, Microbes, and Hippocampal Metabolomics
Project Summary:Examining the role of malnutrition and gut microbes on CNS function using the MAL-BG murine model. RP-UPLC-FTMS was conducted on murine hippocampal tissue.
Institute:University of British Columbia
Department:Microbiology and Immunology
Laboratory:Finlay
Last Name:Bauer
First Name:Kylynda
Address:#301 – 2185 East Mall, University of British Columbia Vancouver, British Columbia Canada, V6T 1Z4
Email:kcbauer@msl.ubc.ca
Phone:(604) 822-2210
Contributors:B. Brett Finlay

Subject:

Subject ID:SU001440
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Genotype Strain:C57BL/6J
Age Or Age Range:7 weeks
Gender:Female
Animal Animal Supplier:Jackson Laboratories

Factors:

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

mb_sample_id local_sample_id Treatment Diet Bacterial Exposure
SA099362CON_1CON Healthy No
SA099363CON_2CON Healthy No
SA099364CON_5CON Healthy No
SA099365CON_3CON Healthy No
SA099366CON_4CON Healthy No
SA099367MALBG_3MAL-BG Malnourished Yes
SA099368MALBG_1MAL-BG Malnourished Yes
SA099369MALBG_2MAL-BG Malnourished Yes
SA099370MALBG_5MAL-BG Malnourished Yes
SA099371MALBG_4MAL-BG Malnourished Yes
SA099372MAL_3MAL Malnourished No
SA099373MAL_1MAL Malnourished No
SA099374MAL_2MAL Malnourished No
SA099375MAL_4MAL Malnourished No
SA099376MAL_5MAL Malnourished No
Showing results 1 to 15 of 15

Collection:

Collection ID:CO001435
Collection Summary:Following sacrifice, murine liver lobes were isolated and stored at -70/80 C prior to untargeted metabolomics.
Sample Type:Hippocampus

Treatment:

Treatment ID:TR001455
Treatment Summary:CON = control mice on healthy diet, MAL = mice placed on a protein/fat deficient diet (malnourished), MAL-BG = MAL mice plus iterative E.coli/Bacteroidales exposure

Sample Preparation:

Sampleprep ID:SP001448
Sampleprep Summary:Methods reported in methodology .zip folder / Metabolomics were completed by TMIC (The Metabolomics Innovation Centre). Each mouse hippocampal sample in an Eppendorf tube was mixed with water, 5 μL per mg of the tissue, and two 4-mm metal balls were added. The tissue was homogenized on a MM 400 mill mixer at a vibrating frequency of 30 Hz for 1 min twice. After 5-s spin-down, a mixture of methanol-chloroform (4:1) was added, at 25 μL per mg tissue, to each tube. The sample was homogenized again for metabolite extraction using the same setup for 1 min twice, followed by sonication in an ice-water bath for 5 min. The tube was centrifuged at 15,000 rpm and at 10 0C for 20 min. The clear supernatant was transferred to a 1.5-mL Eppendorf tube. A 60-μL aliquot from each sample was dried down inside the same nitrogen evaporator and the residue was reconstituted in 40 μL of 80% methanol. 10 μL was injected for reversed-phase (RP)-UPLC-FTMS. Two rounds of sample injections were made, with positive- and negative-ion detection, respectively.

Combined analysis:

Analysis ID AN002273 AN002274
Analysis type MS MS
Chromatography type Reversed phase Reversed phase
Chromatography system Thermo Dionex Ultimate 3000 Thermo Dionex Ultimate 3000
Column Waters BEH C8 (50 x 2.1mm,1.7um) Waters BEH C8 (50 x 2.1mm,1.7um)
MS Type ESI ESI
MS instrument type Orbitrap Orbitrap
MS instrument name Thermo LTQ-Orbitrap Velos Pro Thermo LTQ-Orbitrap Velos Pro
Ion Mode POSITIVE NEGATIVE
Units abundance abundance

Chromatography:

Chromatography ID:CH001672
Instrument Name:Thermo Dionex Ultimate 3000
Column Name:Waters BEH C8 (50 x 2.1mm,1.7um)
Chromatography Type:Reversed phase

MS:

MS ID:MS002117
Analysis ID:AN002273
Instrument Name:Thermo LTQ-Orbitrap Velos Pro
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:For relative quantitation, the MS instrument was run in the survey scan mode with FTMS detection at a mass resolution of 60,000 FWHM at m/z 400. The mass scan range was m/z 80 to 1800, with a reference lock-mass for real-time calibration. Two UPLC-FTMS datasets were acquired for each sample, one with positive-ion detection and the other with negative-ion detection. LC-MS/MS data was also acquired from each sample set with collision induced dissociation (CID) at different levels of normalized collision energy (from publication methods).
Ion Mode:POSITIVE
  
MS ID:MS002118
Analysis ID:AN002274
Instrument Name:Thermo LTQ-Orbitrap Velos Pro
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:For relative quantitation, the MS instrument was run in the survey scan mode with FTMS detection at a mass resolution of 60,000 FWHM at m/z 400. The mass scan range was m/z 80 to 1800, with a reference lock-mass for real-time calibration. Two UPLC-FTMS datasets were acquired for each sample, one with positive-ion detection and the other with negative-ion detection. LC-MS/MS data was also acquired from each sample set with collision induced dissociation (CID) at different levels of normalized collision energy (from publication methods).
Ion Mode:NEGATIVE
  logo