{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST000686","ANALYSIS_ID":"AN001058","VERSION":"1","CREATED_ON":"June 30, 2017, 12:13 pm"},

"PROJECT":{"PROJECT_TITLE":"Impact of prenatal bisphenol A (BPA) on the lipidomics of the female sheep","PROJECT_TYPE":"MS analysis","PROJECT_SUMMARY":"Gestational exposure of bisphenol A in female sheep induces metabolic phenotype and the impact of BPA on lipidomics is being assessed to determine the mechanism that leads to altered insulin sensitivity","INSTITUTE":"University of Michigan","DEPARTMENT":"Environmental Health Science","LABORATORY":"Padmanabhan Lab","LAST_NAME":"Padmanabhan","FIRST_NAME":"Vasantha","ADDRESS":"Ann Arbor, MI","EMAIL":"vasantha@umich.edu","PHONE":"734-647-0276"},

"STUDY":{"STUDY_TITLE":"Lipodomics and Gestational bisphenol A (BPA) exposure","STUDY_TYPE":"MS analysis","STUDY_SUMMARY":"Gestational BPA exposure in sheep induces metabolic phenotype in sheep characterized by peripheral insulin resistance and increased adipocyte size. Because insulin sensitivity can be regulated by various agents including free fatty acids (FFA), we hypothesize that gestational BPA exposure alters circulating FFA inducing dyslipidemia, a marker of metabolic disorder. Because saturated FFA is associated with insulin resistance, determination of the FFA profile in these species aid in understanding the underlying mechanism. Additionally, because of the non-monotonic nature of responses to BPA exposure dose response studies are also needed. This study will therefore assess plasma lipid profile in sheep exposed to three different doses of BPA prenatally and compared with untreated control animals","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":"4","TOTAL_SUBJECTS":"28","STUDY_COMMENTS":"Metabolic disorders such as obesity and diabetes are currently widespread with epidemic proportions. Recent studies have implicated that these disorders have developmental basis due to maternal exposure to adverse insults including endocrine disruptors such as Bisphenol A (BPA). As BPA is present in maternal serum, amniotic fluid, cord blood taken at birth, placenta, colostrum and breast milk suggests that BPA has developmental impacts. In fact developmental BPA exposure have been linked to intrauterine growth restriction and low birth weight offspring, risk factors for adult cardiometabolic abnormalities. Animal models are helpful to study the effect of developmental BPA exposure and determine associated mechanisms."},

"SUBJECT":{"SUBJECT_TYPE":"Animal","SUBJECT_SPECIES":"Ovis aries","TAXONOMY_ID":"9940"},
"SUBJECT_SAMPLE_FACTORS":[
{
"Subject ID":"SU0018573",
"Sample ID":"S00028709",
"Factors":{"BPA_DOSE":"Control"}
},
{
"Subject ID":"SU0018574",
"Sample ID":"S00028710",
"Factors":{"BPA_DOSE":"Control"}
},
{
"Subject ID":"SU0018575",
"Sample ID":"S00028711",
"Factors":{"BPA_DOSE":"Control"}
},
{
"Subject ID":"SU0018576",
"Sample ID":"S00028712",
"Factors":{"BPA_DOSE":"Control"}
},
{
"Subject ID":"SU0018577",
"Sample ID":"S00028713",
"Factors":{"BPA_DOSE":"Control"}
},
{
"Subject ID":"SU0018578",
"Sample ID":"S00028714",
"Factors":{"BPA_DOSE":"Low"}
},
{
"Subject ID":"SU0018579",
"Sample ID":"S00028715",
"Factors":{"BPA_DOSE":"Low"}
},
{
"Subject ID":"SU0018580",
"Sample ID":"S00028716",
"Factors":{"BPA_DOSE":"Low"}
},
{
"Subject ID":"SU0018581",
"Sample ID":"S00028717",
"Factors":{"BPA_DOSE":"Low"}
},
{
"Subject ID":"SU0018582",
"Sample ID":"S00028718",
"Factors":{"BPA_DOSE":"Low"}
},
{
"Subject ID":"SU0018583",
"Sample ID":"S00028719",
"Factors":{"BPA_DOSE":"Low"}
},
{
"Subject ID":"SU0018584",
"Sample ID":"S00028720",
"Factors":{"BPA_DOSE":"Low"}
},
{
"Subject ID":"SU0018585",
"Sample ID":"S00028721",
"Factors":{"BPA_DOSE":"Low"}
},
{
"Subject ID":"SU0018586",
"Sample ID":"S00028722",
"Factors":{"BPA_DOSE":"Medium"}
},
{
"Subject ID":"SU0018587",
"Sample ID":"S00028723",
"Factors":{"BPA_DOSE":"Medium"}
},
{
"Subject ID":"SU0018588",
"Sample ID":"S00028724",
"Factors":{"BPA_DOSE":"Medium"}
},
{
"Subject ID":"SU0018589",
"Sample ID":"S00028725",
"Factors":{"BPA_DOSE":"Medium"}
},
{
"Subject ID":"SU0018590",
"Sample ID":"S00028726",
"Factors":{"BPA_DOSE":"Medium"}
},
{
"Subject ID":"SU0018591",
"Sample ID":"S00028727",
"Factors":{"BPA_DOSE":"Medium"}
},
{
"Subject ID":"SU0018592",
"Sample ID":"S00028728",
"Factors":{"BPA_DOSE":"Medium"}
},
{
"Subject ID":"SU0018593",
"Sample ID":"S00028729",
"Factors":{"BPA_DOSE":"Medium"}
},
{
"Subject ID":"SU0018594",
"Sample ID":"S00028730",
"Factors":{"BPA_DOSE":"Medium"}
},
{
"Subject ID":"SU0018595",
"Sample ID":"S00028731",
"Factors":{"BPA_DOSE":"Medium"}
},
{
"Subject ID":"SU0018596",
"Sample ID":"S00028732",
"Factors":{"BPA_DOSE":"High"}
},
{
"Subject ID":"SU0018597",
"Sample ID":"S00028733",
"Factors":{"BPA_DOSE":"High"}
},
{
"Subject ID":"SU0018598",
"Sample ID":"S00028734",
"Factors":{"BPA_DOSE":"High"}
},
{
"Subject ID":"SU0018599",
"Sample ID":"S00028735",
"Factors":{"BPA_DOSE":"High"}
},
{
"Subject ID":"SU0018600",
"Sample ID":"S00028736",
"Factors":{"BPA_DOSE":"High"}
}
],
"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":"NEGATIVE"},

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

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}

}