Summary of Study ST000873
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 PR000604. The data can be accessed directly via it's Project DOI: 10.21228/M8M09W This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
Study ID | ST000873 |
Study Title | Maternal Hypoxemia and oxidative stress in the fetus, newborn, and adult. exercise training for peripheral artery disease (part II) |
Study Type | Disease model |
Study Summary | Gestational hypoxia presents a significant stress to an unborn fetus that can lead to significant complications related to fetal growth restriction and resulting in diseases in the newborn as well as those manifesting later in life. Recent evidence indicates that inflammation and oxidative stress are contributing factors to hypoxia-related diseases. The Center for Perinatal Biology at Loma Linda University has studied gestational chronic hypoxia in a sheep model for over 20 years to study dysfunction of vascular and nonvascular tissues derived from mothers, fetuses and offspring. In this project we are attempting to use metabolomics to assess metabolic dysregulation in vascular tissues along with markers of oxidative stress and inflammation in the mother and offspring to determine the extent of dysregulation due to chronic hypoxia. Untargeted metabolomics analysis focused on sheep plasma and arteries from the lung, resistance arteries in the brain, uterine arteries, and cultured human myocytes will be used to explore markers of glucose and lipid metabolism disruption. Targeted analyses of oxylipins and endocannabinoids will be used on the same samples to explore markers of oxidative stress and inflammation, which should be increased during hypoxia. This study should delineate pathways and biomarkers that help explain how hypoxia leads to the development of neonatal as well as adult-onset diseases associated with chronic hypoxia that are inter-related with fetal growth restriction. |
Institute | University of California, Davis |
Department | USDA Western Human Nutrition Research Center |
Laboratory | Newman's Lab |
Last Name | Newman |
First Name | John |
Address | 430 West Health Sciences Dr. Davis, Ca, 95616 |
John.Newman@ars.usda.gov | |
Phone | (530) 752-1009 |
Submit Date | 2017-08-30 |
Raw Data Available | Yes |
Raw Data File Type(s) | mzXML |
Analysis Type Detail | LC-MS |
Release Date | 2017-10-11 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR000604 |
Project DOI: | doi: 10.21228/M8M09W |
Project Title: | Maternal Hypoxemia and oxidative stress in the fetus, newborn, and adult. |
Project Summary: | Gestational hypoxia presents a significant stress to an unborn fetus that can lead to significant complications related to fetal growth restriction and resulting in diseases in the newborn as well as those manifesting later in life. Recent evidence indicates that inflammation and oxidative stress are contributing factors to hypoxia-related diseases. The Center for Perinatal Biology at Loma Linda University has studied gestational chronic hypoxia in a sheep model for over 20 years to study dysfunction of vascular and nonvascular tissues derived from mothers, fetuses and offspring. In this project we are attempting to use metabolomics to assess metabolic dysregulation in vascular tissues along with markers of oxidative stress and inflammation in the mother and offspring to determine the extent of dysregulation due to chronic hypoxia. Untargeted metabolomics analysis focused on sheep plasma and arteries from the lung, resistance arteries in the brain, uterine arteries, and cultured human myocytes will be used to explore markers of glucose and lipid metabolism disruption. Targeted analyses of oxylipins and endocannabinoids will be used on the same samples to explore markers of oxidative stress and inflammation, which should be increased during hypoxia. This study should delineate pathways and biomarkers that help explain how hypoxia leads to the development of neonatal as well as adult-onset diseases associated with chronic hypoxia that are inter-related with fetal growth restriction. |
Institute: | University of California, Davis |
Department: | Genome and Biomedical Sciences Facility |
Laboratory: | WCMC Metabolomics Core |
Last Name: | Fiehn |
First Name: | Oliver |
Address: | 1315 Genome and Biomedical Sciences Facility, 451 Health Sciences Drive, Davis, CA 95616 |
Email: | ofiehn@ucdavis.edu |
Phone: | (530) 754-8258 |
Funding Source: | NIH U24DK097154 |
Subject:
Subject ID: | SU000947 |
Subject Type: | Sheep |
Subject Species: | Ovis aries |
Taxonomy ID: | 9940 |
Gender: | Both |
Factors:
Subject type: Sheep; Subject species: Ovis aries (Factor headings shown in green)
mb_sample_id | local_sample_id | Tissue type | Treatment group | Life stage |
---|---|---|---|---|
SA053311 | S49 | Adipose | Hypoxic | Fetal |
SA053312 | S48 | Adipose | Hypoxic | Fetal |
SA053313 | S50 | Adipose | Hypoxic | Fetal |
SA053314 | S51 | Adipose | Hypoxic | Fetal |
SA053315 | S52 | Adipose | Hypoxic | Fetal |
SA053316 | S47 | Adipose | Hypoxic | Fetal |
SA053317 | S53 | Adipose | Hypoxic | Fetal |
SA053318 | S60 | Adipose | Hypoxic | New Born |
SA053319 | S61 | Adipose | Hypoxic | New Born |
SA053320 | S63 | Adipose | Hypoxic | New Born |
SA053321 | S64 | Adipose | Hypoxic | New Born |
SA053322 | S59 | Adipose | Hypoxic | New Born |
SA053323 | S62 | Adipose | Hypoxic | New Born |
SA053324 | S45 | Adipose | Normoxic | Fetal |
SA053325 | S42 | Adipose | Normoxic | Fetal |
SA053326 | S46 | Adipose | Normoxic | Fetal |
SA053327 | S41 | Adipose | Normoxic | Fetal |
SA053328 | S43 | Adipose | Normoxic | Fetal |
SA053329 | S44 | Adipose | Normoxic | Fetal |
SA053330 | S57 | Adipose | Normoxic | New Born |
SA053331 | S58 | Adipose | Normoxic | New Born |
SA053332 | S54 | Adipose | Normoxic | New Born |
SA053333 | S55 | Adipose | Normoxic | New Born |
SA053334 | S56 | Adipose | Normoxic | New Born |
SA053335 | S23 | Carotid | Hypoxic | Adult non-pregnant |
SA053336 | S21 | Carotid | Hypoxic | Adult non-pregnant |
SA053337 | S24 | Carotid | Hypoxic | Adult non-pregnant |
SA053338 | S107 | Carotid | Hypoxic | Adult non-pregnant |
SA053339 | S25 | Carotid | Hypoxic | Adult non-pregnant |
SA053340 | S26 | Carotid | Hypoxic | Fetal |
SA053341 | S28 | Carotid | Hypoxic | Fetal |
SA053342 | S30 | Carotid | Hypoxic | Fetal |
SA053343 | S27 | Carotid | Hypoxic | Fetal |
SA053344 | S29 | Carotid | Hypoxic | Fetal |
SA053345 | S35 | Carotid | Normoxic | Adult non-pregnant |
SA053346 | S31 | Carotid | Normoxic | Adult non-pregnant |
SA053347 | S33 | Carotid | Normoxic | Adult non-pregnant |
SA053348 | S32 | Carotid | Normoxic | Adult non-pregnant |
SA053349 | S34 | Carotid | Normoxic | Adult non-pregnant |
SA053350 | S37 | Carotid | Normoxic | Fetal |
SA053351 | S36 | Carotid | Normoxic | Fetal |
SA053352 | S38 | Carotid | Normoxic | Fetal |
SA053353 | S40 | Carotid | Normoxic | Fetal |
SA053354 | S39 | Carotid | Normoxic | Fetal |
SA053355 | S68 | Pulmonary Arteries | Hypoxic | Adult non-pregnant |
SA053356 | S65 | Pulmonary Arteries | Hypoxic | Adult non-pregnant |
SA053357 | S67 | Pulmonary Arteries | Hypoxic | Adult non-pregnant |
SA053358 | S66 | Pulmonary Arteries | Hypoxic | Adult non-pregnant |
SA053359 | S100 | Pulmonary Arteries | Hypoxic | Adult non-pregnant |
SA053360 | S98 | Pulmonary Arteries | Hypoxic | Adult non-pregnant |
SA053361 | S99 | Pulmonary Arteries | Hypoxic | Adult non-pregnant |
SA053362 | S88 | Pulmonary Arteries | Hypoxic | Fetal |
SA053363 | S103 | Pulmonary Arteries | Hypoxic | Fetal |
SA053364 | S83 | Pulmonary Arteries | Hypoxic | Fetal |
SA053365 | S84 | Pulmonary Arteries | Hypoxic | Fetal |
SA053366 | S87 | Pulmonary Arteries | Hypoxic | Fetal |
SA053367 | S85 | Pulmonary Arteries | Hypoxic | Fetal |
SA053368 | S74 | Pulmonary Arteries | Hypoxic | New Born |
SA053369 | S97 | Pulmonary Arteries | Hypoxic | New Born |
SA053370 | S96 | Pulmonary Arteries | Hypoxic | New Born |
SA053371 | S101 | Pulmonary Arteries | Normoxic | Adult non-pregnant |
SA053372 | S79 | Pulmonary Arteries | Normoxic | Adult non-pregnant |
SA053373 | S80 | Pulmonary Arteries | Normoxic | Adult non-pregnant |
SA053374 | S81 | Pulmonary Arteries | Normoxic | Adult non-pregnant |
SA053375 | S82 | Pulmonary Arteries | Normoxic | Adult non-pregnant |
SA053376 | S102 | Pulmonary Arteries | Normoxic | Adult non-pregnant |
SA053377 | S104 | Pulmonary Arteries | Normoxic | Fetal |
SA053378 | S91 | Pulmonary Arteries | Normoxic | Fetal |
SA053379 | S89 | Pulmonary Arteries | Normoxic | Fetal |
SA053380 | S93 | Pulmonary Arteries | Normoxic | Fetal |
SA053381 | S105 | Pulmonary Arteries | Normoxic | Fetal |
SA053382 | S106 | Pulmonary Arteries | Normoxic | Fetal |
SA053383 | S72 | Pulmonary Arteries | Normoxic | New Born |
SA053384 | S95 | Pulmonary Arteries | Normoxic | New Born |
SA053385 | S71 | Pulmonary Arteries | Normoxic | New Born |
SA053386 | S13 | Uterine Arteries | Hypoxic | Adult non-pregnant |
SA053387 | S11 | Uterine Arteries | Hypoxic | Adult non-pregnant |
SA053388 | S15 | Uterine Arteries | Hypoxic | Adult non-pregnant |
SA053389 | S12 | Uterine Arteries | Hypoxic | Adult non-pregnant |
SA053390 | S14 | Uterine Arteries | Hypoxic | Adult non-pregnant |
SA053391 | S16 | Uterine Arteries | Hypoxic | Adult pregnant |
SA053392 | S18 | Uterine Arteries | Hypoxic | Adult pregnant |
SA053393 | S20 | Uterine Arteries | Hypoxic | Adult pregnant |
SA053394 | S17 | Uterine Arteries | Hypoxic | Adult pregnant |
SA053395 | S19 | Uterine Arteries | Hypoxic | Adult pregnant |
SA053396 | S5 | Uterine Arteries | Normoxic | Adult non-pregnant |
SA053397 | S1 | Uterine Arteries | Normoxic | Adult non-pregnant |
SA053398 | S2 | Uterine Arteries | Normoxic | Adult non-pregnant |
SA053399 | S3 | Uterine Arteries | Normoxic | Adult non-pregnant |
SA053400 | S4 | Uterine Arteries | Normoxic | Adult non-pregnant |
SA053401 | S7 | Uterine Arteries | Normoxic | Adult pregnant |
SA053402 | S6 | Uterine Arteries | Normoxic | Adult pregnant |
SA053403 | S8 | Uterine Arteries | Normoxic | Adult pregnant |
SA053404 | S9 | Uterine Arteries | Normoxic | Adult pregnant |
SA053405 | S10 | Uterine Arteries | Normoxic | Adult pregnant |
Showing results 1 to 95 of 95 |
Collection:
Collection ID: | CO000941 |
Collection Summary: | Part of the routinely flash frozen samples from the Loma Linda University School of Medicine, Center for Perinatal Biology. |
Sample Type: | Tissue |
Tissue Cell Identification: | Adipose tissue, Carotid, pulmonary arteries, uterine arteries |
Treatment:
Treatment ID: | TR000961 |
Treatment Summary: | To induce chronic hypoxia, pregnant and non-pregnant ewes were transported to the White Mountain Research Station that is owned and operated by the University of California. Animals were housed at the Barcroft Research Station (3800 m) for 100+ days prior to having the pregnant or non-pregnant ewes or 2 week old newborn lambs transported back to Loma Linda for study. |
Sample Preparation:
Sampleprep ID: | SP000954 |
Sampleprep Summary: | After sample randomization, weighed tissue (around 10mg for adipose and 50mg for arteries) in 2 mL polypropylene Eppendorf tube was enriched with deuterated surrogates in 20µL methanol (Tables S1 and S2 from Agrawal, K., L.A. Hassoun, N. Foolad, T.L. Pedersen, R.K. Sivamani, J.W. Newman. 2017. Sweat lipid mediator profiling: a non-invasive approach for cutaneous research. J. Lipid Res. 58:188–195 [EPub: Nov 7, 2016]. doi: 10.1194/jlr.M071738) and 5 μl of BHT/EDTA in 1:1 methanol/water (v/v). A total of 400 μl 1-cyclohexyl uredio, 3-dodecanoic acid / 1-phenyl ureido, 3-hexanoic acid (CUDA / PUHA) in 1:1 methanol/acetonitrile (v/v) was added, the sample ground with 3mm stainless steel beads (two for adipose tissue and 3 for blood vessel tissue) and agitation for 6 min at 1500RPM. Protein precipitate and debris were removed by centrifugation (10 min, 10,000 RCF, 6 °C). The supernatant was filtered by centrifugation through 1 µm PVDF membranes (Millipore, Billerica, MA) at 6 °C and 4,500 RCF for 3 min. The filtrate was stored in glass vials at -20 °C until UPLC-MS/MS analysis. |
Combined analysis:
Analysis ID | AN001478 | AN001479 |
---|---|---|
Analysis type | MS | MS |
Chromatography type | Reversed phase | Reversed phase |
Chromatography system | Waters Acquity | Waters Acquity |
Column | Aquity C18 BEH (100 x 2.1mm,1.7um) | Aquity C18 BEH (100 x 2.1mm,1.7um) |
MS Type | ESI | ESI |
MS instrument type | Triple quadrupole | Triple quadrupole |
MS instrument name | ABI Sciex 6500 QTrap | ABI Sciex 6500 QTrap |
Ion Mode | NEGATIVE | POSITIVE |
Units | Concentration (nM) | Concentration (nM) |
Chromatography:
Chromatography ID: | CH001037 |
Instrument Name: | Waters Acquity |
Column Name: | Aquity C18 BEH (100 x 2.1mm,1.7um) |
Column Temperature: | 60 °C |
Flow Gradient: | See protocol/methods file |
Flow Rate: | 0.25 mL/min |
Internal Standard: | See protocol/methods file |
Retention Time: | See protocol/methods file |
Sample Injection: | 5 µL |
Solvent A: | 100% water; 0.1% acetic acid |
Solvent B: | 90% acetonitrile/ 10% isopropanol |
Analytical Time: | 20 min |
Weak Wash Solvent Name: | 20% methanol, 10% isopropanol |
Weak Wash Volume: | 600 µL |
Strong Wash Solvent Name: | 50:50 Acetonitrile:Methanol |
Strong Wash Volume: | 600 µL |
Chromatography Type: | Reversed phase |
MS:
MS ID: | MS001362 |
Analysis ID: | AN001478 |
Instrument Name: | ABI Sciex 6500 QTrap |
Instrument Type: | Triple quadrupole |
MS Type: | ESI |
Ion Mode: | NEGATIVE |
MS ID: | MS001363 |
Analysis ID: | AN001479 |
Instrument Name: | ABI Sciex 6500 QTrap |
Instrument Type: | Triple quadrupole |
MS Type: | ESI |
Ion Mode: | POSITIVE |