Summary of Study ST002803
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 PR001750. The data can be accessed directly via it's Project DOI: 10.21228/M8H71B 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.
Study ID | ST002803 |
Study Title | Early life metabolic abnormalities in the bone marrow of the offspring of obese mothers |
Study Summary | Obese mothers predispose their babies to develop metabolic disorders and obesity before they are even born. The study used a mouse model of maternal high-fat diet-induced obesity that recapitulates cardiovascular and metabolic abnormalities seen in humans born to obese mothers. to compare the metabolic characteristics of bone marrow cells in newly weaned mice. The results showed that the bone marrow of offspring born to mothers on a high-fat diet primarily used glucose through OXPHOS and presented decreased amino acid metabolism. These metabolic changes were observed in the bone marrow of the offspring at a very young age before any symptomatic metabolic disease was present. |
Institute | Oregon Health and Science University |
Department | Knight Cardiovascular Institute |
Laboratory | Maloyan Lab |
Last Name | Maloyan |
First Name | Alina |
Address | 3181 S.W. Sam Jackson Park Road, Portland, Oregon, 97239-3098, USA |
maloyan@ohsu.edu | |
Phone | 503-494-0012 |
Submit Date | 2023-07-21 |
Raw Data Available | Yes |
Raw Data File Type(s) | cdf |
Analysis Type Detail | GC-MS |
Release Date | 2024-06-18 |
Release Version | 1 |
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Collection:
Collection ID: | CO002903 |
Collection Summary: | Bone marrow cells were isolated as previously reported (35). Briefly, femurs were flushed by 25G5/8 needle with medium containing RPMI1640+2% FBS+10 units/ml Heparin + penicillin and streptomycin. Bits of bones were removed using a sterile 4um nylon cell strainer (Falcon 352340). Cells were dissolved in 50 ml medium and centrifuged at 2000 rpm (900x g), for 10 minutes at 4oC. Cell pellets were then washed twice with 50 ml of serum-free RPMI (RPMI1640+20mM Hepes + penicillin and streptomycin, adjusted to pH 7.4 before filtering), centrifuged at 2000 rpm, at 4oC for 5 minutes, and resuspended in 25 ml of serum-free RPMI. |
Sample Type: | Bone marrow |