Summary of Study ST000522
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 PR000385. The data can be accessed directly via it's Project DOI: 10.21228/M8902F This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
Study ID | ST000522 |
Study Title | Plasma metabolomics profiling for fish maturation in blunt snout bream |
Study Type | Metabolomics experiment |
Study Summary | We investigated the comprehensive metabolic profiles of plasma among immature females, mature females ready to spawn, as well as already spawned breeders of blunt snout bream (Megalobrama amblycephala). The purpose of this study was to screen out potential biomarkers for sexual mature female M. amblycephala compared to immature female individuals and already spawned breeders. The three groups were set up in this study, including one year old immature females, 2 years old sexually mature females ready to spawning and successfully spawning females of M. amblycephala. The plasma samples were collected to investigate the comprehensive metabolic profiles through UPLC-MS/MS based metabolomics analysis method. According to multivariate and univariate statistical analysis, plasma metabolite profiles of three groups were obviously separated, and the plasma metabolite profiles of immature female M. amblycephala were much more different from mature females ready to spawn as well as already spawned breeders. The differential plasma metabolites from three hormone related pathways including GnRH signaling pathway, steroid hormone biosynthesis and steroid biosynthesis, were further analyzed. A total of 29 metabolites were identified as differential biomarkers associated with the female maturation status |
Institute | Huazhong Agricultural University |
Department | College of Fisheries |
Laboratory | Key Lab of Freshwater Animal Breeding, Ministry of Agriculture |
Last Name | Zhou |
First Name | LaiFang |
Address | Hongshan, Wuhan, 430070 Hubei, China |
156851836@qq.com | |
Phone | 15171617087 |
Submit Date | 2016-12-13 |
Raw Data File Type(s) | cdf |
Analysis Type Detail | LC-MS |
Release Date | 2018-12-11 |
Release Version | 1 |
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Combined analysis:
Analysis ID | AN000796 | AN000797 |
---|---|---|
Analysis type | MS | MS |
Chromatography type | Reversed phase | Reversed phase |
Chromatography system | Waters 2777C | Waters 2777C |
Column | Waters Acquity BEH C18 (150 x 2mm,1.7um) | Waters Acquity BEH C18 (150 x 2mm,1.7um) |
MS Type | ESI | ESI |
MS instrument type | QTOF | QTOF |
MS instrument name | Waters Synapt G2 XS QTOF | Waters Synapt G2 XS QTOF |
Ion Mode | POSITIVE | NEGATIVE |
Units | peak intensity | peak intensity |
Chromatography:
Chromatography ID: | CH000572 |
Chromatography Summary: | Chromatographic separation was performed on a ACQUITY UPLC BEH C18 analytical column (100×2.1 mm, 1.7 µm, Waters, Milford, USA) using a 2777C UPLC system (Waters). The flow rate was 0.40 mL/min and the mobile phase was composed of solvents A (95% H2O/5% acetonitrile + 0.1% formic acid) and B (95% acetonitrile/5% H2O+0.1% formic acid).The gradient program was optimized as follows: 0–0.1 min, 100% A; 0.1–0.6 min, 100% A-50% A; 0.6–5 min, 50%–0% A; 5–8 min, 0% A; 8–10 min, 0% A-100% A. Injection volume was 10 µl. The eluent from the column was directly added in to the mass spectrometer without split. |
Instrument Name: | Waters 2777C |
Column Name: | Waters Acquity BEH C18 (150 x 2mm,1.7um) |
Flow Gradient: | 100% acetonitrile |
Flow Rate: | 0.40 mL/min |
Solvent A: | 95% water/5% acetonitrile; 0.1% formic acid |
Solvent B: | 95% acetonitrile/5% water; 0.1% formic acid |
Chromatography Type: | Reversed phase |