Summary of Study ST001245

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 PR000832. The data can be accessed directly via it's Project DOI: 10.21228/M84Q24 This work is supported by NIH grant, U2C- DK119886.

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Study IDST001245
Study TitleLuteal lipids regulate progesterone production and may modulate immune cell function during the estrous cycle and pregnancy
Study SummaryDespite data indicating an important functional role for bioactive lipids in luteal function, little is known about the patterns of abundance of these lipids in corpus luteum (CL) during luteal development, maintenance, and rescue, in any species. Therefore, the abundance of lipid mediators, including endocannabinoids and oxylipins from cyclooxygenase (COX), lipoxygenase (LOX), and cytochrome P450 (CYP)-dependent metabolism were profiled in the CL on days 4, 11, and 18 of the estrous cycle and on day 18 of pregnancy. The objectives of this study were to identify lipid mediators that regulate luteal function during these transitions, to integrate the lipid profile with a previously published mRNA profile of CL during maternal recognition of pregnancy, and to determine the effect of a subset of lipids on in vitro progesterone production.
Institute
University of California, Davis
DepartmentGenome and Biomedical Sciences Facility
LaboratoryWCMC Metabolomics Core
Last NameFiehn
First NameOliver
Address1315 Genome and Biomedical Sciences Facility, 451 Health Sciences Drive, Davis, CA 95616
Emailofiehn@ucdavis.edu
Phone(530) 754-8258
Submit Date2019-07-29
PublicationsHughes, C.H.K., R. Bosviel, J.W. Newman, J.L. Pate. Luteal lipids regulate progesterone production and may modulate immune cell function during the estrous cycle and pregnancy. Front. Endocrinol. Jun 27, 2019
Raw Data AvailableYes
Raw Data File Type(s)wiff
Analysis Type DetailLC-MS
Release Date2019-09-10
Release Version1
Oliver Fiehn Oliver Fiehn
https://dx.doi.org/10.21228/M84Q24
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Factors:

Subject type: Mammal; Subject species: Bos taurus (Factor headings shown in green)

mb_sample_id local_sample_id Treatment
SA090787971D18 cyclic
SA0907881022D18 cyclic
SA0907891008D18 cyclic
SA0907901012D18 cyclic
SA0907911011D18 pregnant
SA0907921021D18 pregnant
SA0907931020D18 pregnant
SA0907941025D18 pregnant
SA0907951005Early
SA0907961106Early
SA0907971006Early
SA0907981007Early
SA090799957Midcycle
SA090800936Midcycle
SA0908011129Midcycle
SA090802956Midcycle
SA090806876Regressing 12 hour
SA090807912Regressing 12 hour
SA090808909Regressing 12 hour
SA090809905Regressing 12 hour
SA090803604Regressing 1 hour
SA090804600Regressing 1 hour
SA090805858Regressing 1 hour
SA0908101379Regressing 24 hour
SA0908111378Regressing 24 hour
SA0908121380Regressing 24 hour
SA0908131381Regressing 24 hour
SA090814616Regressing 4 hour
SA090815575Regressing 4 hour
SA090816862Regressing 4 hour
SA090817857Regressing 4 hour
SA0908181352Regressing 8 hour
SA0908191342Regressing 8 hour
SA0908201351Regressing 8 hour
SA0908211353Regressing 8 hour
Showing results 1 to 35 of 35
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