{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST000675","ANALYSIS_ID":"AN001037","VERSION":"1","CREATED_ON":"June 30, 2017, 10:44 am"},

"PROJECT":{"PROJECT_TITLE":"Effects of rosiglitazone treatment on lipid composition","PROJECT_TYPE":"MS analysis","PROJECT_SUMMARY":"rosiglitazone treatment of human adipose tissue","INSTITUTE":"Boston University","DEPARTMENT":"Department of Medicine","LABORATORY":"Lee, Mi-Jeong Lab","LAST_NAME":"Lee","FIRST_NAME":"Mi-Jeong","ADDRESS":"Boston, MA","EMAIL":"lee.mijeong@gmail.com","PHONE":"617-429-2669"},

"STUDY":{"STUDY_TITLE":"Effects of rosiglitazone treatment on lipid composition","STUDY_TYPE":"MS analysis","STUDY_SUMMARY":"Reprograming of 'white' to 'brite' adipocytes with higher oxidative capacity and improved endocrine function represents a potentially important approach to address the dysfunctional adipocyte phenotypes in obesity. We find that chronic treatment with the PPAR? agonist (rosiglitazone, 1 uM for 7days in vitro) in white human adipose tissue induced metabolic changes. Our trancriptome analysis showed that higher mitochondrial and peroxisomal fatty acid oxidation pathways and other genes involved in lipid metabolism including (re)esterification are induced by rosiglitazone treatment. To understand the biochemical basis of brite vs. white human adipocytes, we will perform comprehensive metabolomic profiling of control and rosiglitazone treated tissues using unbiased lipidomics approach.","INSTITUTE":"University of Michigan","DEPARTMENT":"Biomedical Research Core Facilities","LABORATORY":"Metabolomics core","LAST_NAME":"Kachman","FIRST_NAME":"Maureen","ADDRESS":"6300 Brehm Tower, 1000 Wall Street, Ann Arbor, MI 48105-5714","EMAIL":"mkachman@med.umich.edu","PHONE":"(734) 232-8175","NUM_GROUPS":"2","TOTAL_SUBJECTS":"4"},

"SUBJECT":{"SUBJECT_TYPE":"Human","SUBJECT_SPECIES":"Homo sapiens","TAXONOMY_ID":"9606"},
"SUBJECT_SAMPLE_FACTORS":[
{
"Subject ID":"SU0014815",
"Sample ID":"S00022664",
"Factors":{"TYPE":"control"}
},
{
"Subject ID":"SU0014815",
"Sample ID":"S00022665",
"Factors":{"TYPE":"control"}
},
{
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"Sample ID":"S00022666",
"Factors":{"TYPE":"Rosi"}
},
{
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"Sample ID":"S00022667",
"Factors":{"TYPE":"Rosi"}
},
{
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"Sample ID":"S00022668",
"Factors":{"TYPE":"control"}
},
{
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"Sample ID":"S00022669",
"Factors":{"TYPE":"control"}
},
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"Sample ID":"S00022670",
"Factors":{"TYPE":"Rosi"}
},
{
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"Sample ID":"S00022671",
"Factors":{"TYPE":"Rosi"}
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{
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"Sample ID":"S00022672",
"Factors":{"TYPE":"control"}
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"Sample ID":"S00022673",
"Factors":{"TYPE":"control"}
},
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"Factors":{"TYPE":"Rosi"}
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{
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"Sample ID":"S00022676",
"Factors":{"TYPE":"control"}
},
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"Sample ID":"S00022677",
"Factors":{"TYPE":"control"}
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"Factors":{"TYPE":"Rosi"}
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{
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"Sample ID":"S00022679",
"Factors":{"TYPE":"Rosi"}
}
],
"COLLECTION":{"COLLECTION_SUMMARY":"-"},

"TREATMENT":{"TREATMENT_SUMMARY":"-"},

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"-","SAMPLEPREP_PROTOCOL_FILENAME":"A004 - Shotgun Lipidomics.pdf"},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_TYPE":"Reversed phase","INSTRUMENT_NAME":"ABI Sciex 5600+ TripleTOF","COLUMN_NAME":"Waters Acquity HSS T3 (50 x 2.1mm, 1.8um)"},

"ANALYSIS":{"ANALYSIS_TYPE":"MS","ANALYSIS_PROTOCOL_FILE":"A004 - Shotgun Lipidomics.pdf"},

"MS":{"MS_COMMENTS":"-","INSTRUMENT_NAME":"ABI Sciex 5600+ TripleTOF","INSTRUMENT_TYPE":"Triple TOF","MS_TYPE":"ESI","ION_MODE":"POSITIVE"},

"MS_METABOLITE_DATA":{
"Units":"peak area normalized",

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}

}