{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST001632","ANALYSIS_ID":"AN002668","VERSION":"1","CREATED_ON":"December 15, 2020, 12:38 pm"},

"PROJECT":{"PROJECT_TITLE":"Lipidomics of Ginseng Total Secondary Saponins on Myocardial Ischemia Rat","PROJECT_SUMMARY":"Cardioprotective Effect of Ginseng Total Secondary Saponins on Myocardial Ischemia Rat via Regulating Disturbed Lipids Based on Lipidomics.","INSTITUTE":"Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College","LAST_NAME":"Wang","FIRST_NAME":"Zhe","ADDRESS":"No.2 nanwei street, xichen district, Beijing, China","EMAIL":"wangzhe@imm.ac.cn","PHONE":"+861083154880"},

"STUDY":{"STUDY_TITLE":"Lipidomics of Ginseng Total Secondary Saponins on Myocardial Ischemia Rat","STUDY_SUMMARY":"Cardioprotective Effect of Ginseng Total Secondary Saponins on Myocardial Ischemia Rat via Regulating Disturbed Lipids Based on Lipidomics.","INSTITUTE":"Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College","LAST_NAME":"Wang","FIRST_NAME":"Zhe","ADDRESS":"No.2 nanwei street, xichen district, Beijing, China","EMAIL":"wangzhe@imm.ac.cn","PHONE":"+861083154880"},

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"Sample ID":"8-A4-HS",
"Factors":{"class":"GTSS","Tissue":"heart"},
"Additional sample data":{"RAW_FILE_NAME":"140604054.d","lipid":"Sph/Cer/CoQ"}
},
{
"Subject ID":"-",
"Sample ID":"8-B2-HS",
"Factors":{"class":"GTSS","Tissue":"heart"},
"Additional sample data":{"RAW_FILE_NAME":"140604056.d","lipid":"Sph/Cer/CoQ"}
},
{
"Subject ID":"-",
"Sample ID":"8-B3-HS",
"Factors":{"class":"GTSS","Tissue":"heart"},
"Additional sample data":{"RAW_FILE_NAME":"140604057.d","lipid":"Sph/Cer/CoQ"}
},
{
"Subject ID":"-",
"Sample ID":"8-C5-HS",
"Factors":{"class":"GTSS","Tissue":"heart"},
"Additional sample data":{"RAW_FILE_NAME":"140604058.d","lipid":"Sph/Cer/CoQ"}
}
],
"COLLECTION":{"COLLECTION_SUMMARY":"Blood samples of the rats were collected to obtain plasma by centrifugation (3000r/min, 15 min) using heparin as an anticoagulant and kept at -80℃ until analysis. Hearts were collected, washed with cold saline and cut in half. One part was grinded into powder in liquid nitrogen and kept at -80℃. Heart samples were homogenized in saline on ice at the ratio of tissue to solution was 1:4 (w/v) before analysis.","SAMPLE_TYPE":"Heart"},

"TREATMENT":{"TREATMENT_SUMMARY":"Rats were divided into six rats in each group randomly as following: control rats group, MI model rats group, MI model rats pre-treated with diltiazem group (50 mg/kg, i.g.), and MI model rats pre-treated with GTSS group (200 mg/kg, i.g.). Pre-treated rats were consecutively administrated for 4 weeks. Except control rats group received saline, other rat groups received two injections of isoproterenol (85 mg/kg, s.c.) on the 27th and 28th days at an interval of 24 hours."},

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"100μl of plasma or tissue homogenate was transferred into a 10 ml glass tube and added 20 μl of lipid internal standards. After vortexed for 10 s, 1.5 ml of methanol and 5 ml methyl tert-butyl ether were added to the tube, and the sample was vortexed for 15 min and then added 1.5 ml water, then centrifuged at 4500r/min for 10 min (4 ℃). The upper organic phase was transferred to another glass tube, and the lower water phase was added with 2 ml secondary extractant (methyl tert-butyl ether /methanol/water,10:3:2.5, v/v/v). After vortexed for 10min and centrifuged for 15min at 4500rpm, and the upper organic phase was combined and dried under a gentle nitrogen stream. The residue was re-dissolved in 100 μl methanol/chloroform (1:1, v/v)."},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_TYPE":"Reversed phase","INSTRUMENT_NAME":"Thermo Accela 1250","COLUMN_NAME":"Waters Xterra MS C8 (2.1×100mm,3.5µm)"},

"ANALYSIS":{"ANALYSIS_TYPE":"MS"},

"MS":{"INSTRUMENT_NAME":"Thermo LTQ-FT","INSTRUMENT_TYPE":"LTQ-FT","MS_TYPE":"ESI","ION_MODE":"UNSPECIFIED","MS_COMMENTS":"The LTQ-FT was run in full-scan mode at 100000 resolution from m/z50–1200 with MS parameters: sheath gas flow rate, 50 arb; aux gas flow rate, 20 arb; sweep gas flow rate, 3 arb; capillary temperature, 275 ℃ in both positive and negative mode. And spray voltage, 4.5kV; capillary voltage, 35.0V; tube lens, 120V were used for the positive mode. Spray voltage, -4.0kV; capillary voltage, -35.0V; tube lens, -120V were used for the negative mode."},

"MS_METABOLITE_DATA":{
"Units":"pmol/ml(PL) & pmol/mg(HL)",

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}

}