Summary of Study ST002648

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 PR001020. The data can be accessed directly via it's Project DOI: 10.21228/M8V97D 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 IDST002648
Study TitleMoTrPAC: Endurance exercise training study in young adult rats, Tissue:Vastus Lateralis - Untargeted HILIC-Positive
Study SummaryThe goal of the endurance exercise training study in young adult rats (internal code: PASS1B-06) was to perform exercise training studies in adult (6 month) F344 rats, and from these rats collect as many tissues as feasible in order to provide high quality samples for detailed analysis by chemical analysis sites. Tissues were collected from 10-12 rats sedentary control rats concurrent with the collection of the 8-week training groups. The 8-week training group and controls were from the same cohort and same age at euthanasia (either 8). For the older age group, an additional set of controls (n=5-6) were collected with the 1-2 week training group. Rats were either sedentary or underwent an exercise training program. Rats were exercised on the rodent treadmill 5 days per week using a progressive training protocol designed to exercise the rats at approximately 70% of VO2max as outlined in the Table on the next page. Training was performed no earlier than 10:00 am and no later than 5:00 pm over 5 consecutive days per week. Training was initiated with the treadmill set at 70% of VO2 max (see tables) and 5 degrees grade for 20 minutes. The duration of exercise was increased by one minute each day until day 31 of training (start of week 7), when a duration of 50 min was reached. Speed and grade of each training session increased in larger increments due to treadmill parameters. The highest intensity and duration of training began on day 31. This intensity was maintained for the final 10 days of the protocol to ensure steady state had been achieved. If any rats were unable to perform at least 4 days of training per week they were removed from the study and euthanized. It is important to note that the starting treadmill speed varied depending on the sex and age of the rat. The initial and maximum speeds were based on VO2max measurements obtained during the pre-training testing of the compliant rats. Rats assigned to the control group followed a schedule similar to the training group. They were placed in one lane on the treadmill for 15 minutes/day, 5 days per week. The treadmill was set at 0 m/min at an incline that corresponded to the incline being used by the training group.
Institute
Broad Institute of MIT and Harvard
DepartmentMetabolomics Platform
LaboratoryClish
Last NameClish
First NameClary
Address415 Main St, Cambridge, MA 02142
Emailclary@broadinstitute.org
Phone(617) 714-7654
Submit Date2023-05-01
Raw Data AvailableYes
Raw Data File Type(s)TBD
Analysis Type DetailLC-MS
Release Date2023-10-06
Release Version1
Clary Clish Clary Clish
https://dx.doi.org/10.21228/M8V97D
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR001020
Project DOI:doi: 10.21228/M8V97D
Project Title:MoTrPAC
Project Summary:MoTrPAC is a national research consortium designed to discover and perform preliminary characterization of the range of molecular transducers (the "molecular map") that underlie the effects of physical activity in humans. The program's goal is to study the molecular changes that occur during and after exercise and ultimately to advance the understanding of how physical activity improves and preserves health. Preclinical and clinical studies will examine the systemic effects of endurance and resistance exercise across a range of ages and fitness levels by molecular probing of multiple tissues before and after acute and chronic exercise. This program is the largest targeted NIH investment of funds into the mechanisms of how physical activity improves health and prevents disease. The MoTrPAC program is supported by the NIH Common Fund and is managed by a trans-agency working group representing multiple NIH institutes and centers, led by the NIH Office of Strategic Coordination, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute on Aging, and National Institute of Biomedical Imaging and Bioengineering. MoTrPAC Steering Committee: Wendy Kohrt, Chair, Russ Tracy, Co-Chair; NIH Program Manager, Concepcion Nierras. Euan Ashley and Matthew Wheeler are the PIs for the Motrpac Bioinformatics / Data Coordination Center.
Institute:MoTrPAC
Last Name:Ashley
First Name:Euan
Address:Falk Building CV267, 870 Quarry Road, Stanford, California 94305
Email:motrpac-data-deposition@lists.stanford.edu
Phone:(650) 725-1846

Subject:

Subject ID:SU002750
Subject Type:Mammal
Subject Species:Rattus norvegicus
Taxonomy ID:10116

Factors:

Subject type: Mammal; Subject species: Rattus norvegicus (Factor headings shown in green)

mb_sample_id local_sample_id Group Timepoint Sex
SA26320590245015604Control 8 weeks of training or control time Female
SA26320690248015604Control 8 weeks of training or control time Female
SA26320790252015604Control 8 weeks of training or control time Female
SA26320890266015604Control 8 weeks of training or control time Female
SA26320990265015604Control 8 weeks of training or control time Female
SA26321090237015604Control 8 weeks of training or control time Male
SA26321190229015604Control 8 weeks of training or control time Male
SA26321290239015604Control 8 weeks of training or control time Male
SA26321390217015604Control 8 weeks of training or control time Male
SA26321490232015604Control 8 weeks of training or control time Male
SA263215QC_PREFA03QC-DriftCorrection 0 hour -
SA263216QC_PREFA01QC-DriftCorrection 0 hour -
SA263217QC_PREFA02QC-DriftCorrection 0 hour -
SA263218QC_PREFA04QC-DriftCorrection 0 hour -
SA263219QC_PREFB02QC-Pooled 0 hour -
SA263220QC_PREFB04QC-Pooled 0 hour -
SA263221QC_PREFB01QC-Pooled 0 hour -
SA263222QC_PREFB03QC-Pooled 0 hour -
SA263223QC_Sed02QC-Reference 0 hour -
SA263224QC_IPE01QC-Reference 0 hour -
SA263225QC_IPE04QC-Reference 0 hour -
SA263226QC_IPE03QC-Reference 0 hour -
SA263227QC_Sed01QC-Reference 0 hour -
SA263228QC_Sed04QC-Reference 0 hour -
SA263229QC_IPE02QC-Reference 0 hour -
SA263230QC_Sed03QC-Reference 0 hour -
SA26323190564015604Training 1 week of training or control time Female
SA26323290567015604Training 1 week of training or control time Female
SA26323390559015604Training 1 week of training or control time Female
SA26323490560015604Training 1 week of training or control time Female
SA26323590571015604Training 1 week of training or control time Female
SA26323690423015604Training 1 week of training or control time Male
SA26323790426015604Training 1 week of training or control time Male
SA26323890430015604Training 1 week of training or control time Male
SA26323990421015604Training 1 week of training or control time Male
SA26324090422015604Training 1 week of training or control time Male
SA26324190578015604Training 2 weeks of training Female
SA26324290587015604Training 2 weeks of training Female
SA26324390581015604Training 2 weeks of training Female
SA26324490585015604Training 2 weeks of training Female
SA26324590576015604Training 2 weeks of training Female
SA26324690449015604Training 2 weeks of training Male
SA26324790444015604Training 2 weeks of training Male
SA26324890439015604Training 2 weeks of training Male
SA26324990450015604Training 2 weeks of training Male
SA26325090441015604Training 2 weeks of training Male
SA26325190406015604Training 4 weeks of training Female
SA26325290420015604Training 4 weeks of training Female
SA26325390410015604Training 4 weeks of training Female
SA26325490412015604Training 4 weeks of training Female
SA26325590416015604Training 4 weeks of training Female
SA26325690280015604Training 4 weeks of training Male
SA26325790281015604Training 4 weeks of training Male
SA26325890289015604Training 4 weeks of training Male
SA26325990292015604Training 4 weeks of training Male
SA26326090283015604Training 4 weeks of training Male
SA26326190251015604Training 8 weeks of training or control time Female
SA26326290254015604Training 8 weeks of training or control time Female
SA26326390267015604Training 8 weeks of training or control time Female
SA26326490258015604Training 8 weeks of training or control time Female
SA26326590259015604Training 8 weeks of training or control time Female
SA26326690222015604Training 8 weeks of training or control time Male
SA26326790218015604Training 8 weeks of training or control time Male
SA26326890225015604Training 8 weeks of training or control time Male
SA26326990227015604Training 8 weeks of training or control time Male
SA26327090223015604Training 8 weeks of training or control time Male
Showing results 1 to 66 of 66

Collection:

Collection ID:CO002743
Collection Summary:-
Sample Type:Vastus lateralis

Treatment:

Treatment ID:TR002759
Treatment Summary:-

Sample Preparation:

Sampleprep ID:SP002756
Sampleprep Summary:Tissue samples (10 mg) were homogenized in 300 µL of 10/67.4/22.4/0.18 (v/v/v/v) water/acetonitrile/methanol/formic acid containing stable isotope-labeled internal standards (0.18 ng/µL valine-d8, Isotec; 0.18 ng/µL phenylalanine-d8, Cambridge Isotope Laboratories) using a TissueLyserII bead mill (20 Hz, 2 X 2min; QIAGEN). The samples were place in a -80?C freezer for one hour and then centrifuged for 10 min (9000g, 4?C). 100uL of each supernatent was transferred to a de-activated inserts within an autsampler vial (Waters).
Sampleprep Protocol Filename:pass1b_experimental_design_metabolomics.pdf

Combined analysis:

Analysis ID AN004320
Analysis type MS
Chromatography type HILIC
Chromatography system Shimadzu Nexera X2
Column Waters Atlantis HILIC (150 x 2.1mm,3um)
MS Type ESI
MS instrument type Orbitrap
MS instrument name Thermo Q Exactive Orbitrap
Ion Mode POSITIVE
Units peak area

Chromatography:

Chromatography ID:CH003226
Chromatography Summary:Extracts (10 µL) were injected onto a 150 x 2.1 mm Atlantis HILIC column (Waters). The column was eluted isocratically at a flow rate of 250 µL/min with 5% mobile phase A (10 mM ammonium formate and 0.1% formic acid in water) for 1 minute followed by a linear gradient to 40% mobile phase B (acetonitrile with 0.1% formic acid) over 10 minutes
Methods Filename:pass1b_hilicpos_methods.pdf
Instrument Name:Shimadzu Nexera X2
Column Name:Waters Atlantis HILIC (150 x 2.1mm,3um)
Column Temperature:-
Flow Gradient:The column was eluted isocratically at a flow rate of 250 µL/min with 5% mobile phase A for 1 minute followed by a linear gradient to 40% mobile phase B over 10 minutes
Flow Rate:250 µL/min
Solvent A:100% water; 0.1% formic acid; 10 mM ammonium formate
Solvent B:100% acetonitrile; 0.1% formic acid
Chromatography Type:HILIC

MS:

MS ID:MS004067
Analysis ID:AN004320
Instrument Name:Thermo Q Exactive Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:High resolution, accurate mass data were acquired using a system comprised of a Shimadzu Nexera X2 U-HPLC (Shimadzu Corp.; Marlborough, MA) coupled to a Q Exactive hybrid quadrupole orbitrap mass spectrometer (Thermo Fisher Scientific; Waltham, MA). MS analyses were carried out using electrospray ionization in the positive ion mode using full scan analysis over 70-800 m/z at 70,000 resolution and 3 Hz data acquisition rate. Other MS settings were: sheath gas 40, sweep gas 2, spray voltage 3.5 kV, capillary temperature 350°C, S-lens RF 40, heater temperature 300°C, microscans 1, automatic gain control target 1e6, and maximum ion time 250 ms. Raw data were processed using TraceFinder software (Thermo Fisher Scientific; Waltham, MA) and Progenesis QI (Nonlinear Dynamics; Newcastle upon Tyne, UK). The identities of 202 profiled metabolites were confirmed using reference standards.
Ion Mode:POSITIVE
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