{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST001273","ANALYSIS_ID":"AN002113","VERSION":"1","CREATED_ON":"November 11, 2019, 10:35 am"},

"PROJECT":{"PROJECT_TITLE":"Lipidomics Dataset of Sonication-Induced Traumatic Optic Neuropathy in Mice","PROJECT_SUMMARY":"Traumatic optic neuropathy (TON) is the loss of vision secondary to trauma. Approximately two weeks after traumatic damage, diffuse retinal ganglion cell loss and axon degeneration of the optic nerve are exhibited. Here we presented the changes that occured in the optic nerve lipidome of two-month-old C57BL/6J mice following sonication-induced TON Optic nerves were harvested at three time points following injury: 1-day, 7-days, and 14-days for comparison with the control group (uninjured optic nerves from 2-month-old mice). Lipidomic changes were observed at each of the various time points, with a pattern of progression present in multiple lipid classes.","INSTITUTE":"Bascom Palmer Eye Institute, Miller School of Medicine at University of Miami, Miami, FL 33136, USA","DEPARTMENT":"Ophthalmology, Bascom Palmer Eye Institute","LAST_NAME":"Bhattacharya","FIRST_NAME":"Sanjoy K","ADDRESS":"1638 NW 10th Avenue, Suite 707A University of Miami Miami, FL, 33136","EMAIL":"SBhattacharya@med.miami.edu","PHONE":"305-482-4103"},

"STUDY":{"STUDY_TITLE":"Lipidomics Dataset of Sonication-Induced Traumatic Optic Neuropathy in Mice","STUDY_SUMMARY":"Traumatic optic neuropathy (TON) is the loss of vision secondary to trauma. Approximately two weeks after traumatic damage, diffuse retinal ganglion cell loss and axon degeneration of the optic nerve are exhibited. Here we present the changes that occur in the optic nerve lipidome of two-month-old C57BL/6J mice following sonication-induced TON (SI-TON), which closely models the indirect clinical mechanism in TON. Optic nerves were harvested at three time points following injury: 1-day, 7-days, and 14-days for comparison with the control group (uninjured optic nerves from 2-month-old mice). Lipidomic changes were observed at each of the various time points, with a pattern of progression present in multiple lipid classes. This data demonstrates the distinct lipidomic changes at each time point following indirect trauma to the optic nerve.","INSTITUTE":"Bascom Palmer Eye Institute, Miller School of Medicine at University of Miami, Miami, FL 33136, USA","DEPARTMENT":"Ophthalmology, Bascom Palmer Eye Institute","LAST_NAME":"Bhattacharya","FIRST_NAME":"Sanjoy K","ADDRESS":"1638 NW 10th Avenue, Suite 707A University of Miami Miami, FL, 33136","EMAIL":"SBhattacharya@med.miami.edu","PHONE":"305-482-4103","NUM_GROUPS":"4","TOTAL_SUBJECTS":"31","NUM_MALES":"15","NUM_FEMALES":"16"},

"SUBJECT":{"SUBJECT_TYPE":"Mammal","SUBJECT_SPECIES":"Mus musculus","TAXONOMY_ID":"10090","GENOTYPE_STRAIN":"C57BL/6J","AGE_OR_AGE_RANGE":"2 Months","GENDER":"Male and female"},
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"COLLECTION":{"COLLECTION_SUMMARY":"Mice were exposed to a controlled sonication pulse and optic nerve samples were collected at 1 day, 7 days, and 14 days post sonication. Lipids were then extracted, resuspended in Chloroform:Methanol (1:1) and processed through untargeted liquid chromatography Q-Exactive Orbitrap tandem mass spectrometry (LC-MS/MS).","SAMPLE_TYPE":"optic nerve"},

"TREATMENT":{"TREATMENT_SUMMARY":"Mice were exposed to a 500msec sonication shock at the supraorbital rim that did not create any skull fractures nor cause death. Mice were sacrificed at 1 day, 7 days, or 14 days post exposure for lipid analysis of optic nerves."},

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"As described in collection"},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_TYPE":"Reversed phase","INSTRUMENT_NAME":"Thermo Accela 600","COLUMN_NAME":"Thermo Acclaim C18 (150 x 2.1mm, 3µm)"},

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

"MS":{"INSTRUMENT_NAME":"Thermo Q Exactive Orbitrap","INSTRUMENT_TYPE":"Orbitrap","MS_TYPE":"ESI","ION_MODE":"POSITIVE","MS_COMMENTS":"A Heated Electrospray Ionization Source (HESI) was operated at a spray voltage of 4.4kV, a HESI vaporization temperature of 275°C, a sheath gas pressure of 45 arbitrary units, and an auxillary gas flow of 15 arbitrary units. The ion transfer tube was kept at a temperature of 350°C. The scan range was set at 150-1500 m/z."},

"MS_METABOLITE_DATA":{
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