Comparison of different liquid chromatography stationary phases in LC-HRMS metabolomics for the detection of recombinant growth hormone doping control.
Abstract: Growth hormone (GH) is a polypeptide suspected of being used in horse racing to speed up physical performances. Despite scientific advances in the recent years, the control of its administration remains difficult. In order to improve it, a metabolomics study through LC-high resolution mass spectrometry measurements was recently initiated to assess the metabolic perturbations caused by recombinant equine growth hormone administration. Few tens of ions not identified structurally were highlighted as compounds responsible for the modification of metabolic profiling observed in treated animals. This previous work was based on the use of Uptisphere Strategy NEC as the chromatographic column. In parallel, more and more metabolomics studies showed the interest of the use of new chromatographic supports such as hydrophilic interaction chromatography for the analysis of polar compounds. It is in this context that an investigation was conducted on Uptisphere HDO and Luna hydrophilic interaction chromatography stationary phases to generate and process urinary metabolomics fingerprints, which could allow to establish a comparison with Uptisphere Strategy NEC. The chromatographic column the most adapted for the detection of new biomarkers of GH administration has been used to set up a relevant statistical model based on the analysis of more than hundred biological samples.
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication Date: 2011-06-27 PubMed ID: 21710695DOI: 10.1002/jssc.201100223Google Scholar: Lookup
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research article involves devising a better method to detect the administration of growth hormone (GH) in horse racing, a substance believed to enhance performance. The study examined the use of different liquid chromatography stationary phases in combination with high-resolution mass spectrometry metabolism studies to discern changes caused by equine growth hormone use.
Objective of the Research
- The research aimed to increase the efficiency of detecting growth hormone usage in horse racing. This was attempted by studying metabolomics, specifically how the hormone altered the metabolic profile of the treated animals.
- The researchers also intended to compare the effects of using different chromatographic columns, including Uptisphere Strategy NEC, Uptisphere HDO and Luna hydrophilic interaction chromatography phases.
Methodology and Approach
- The scientific team conducted a metabolomics study using LC-high resolution mass spectrometry to examine metabolic changes caused by injecting horses with equine growth hormones.
- The team identified several ions responsible for altering the metabolic profiles of the treated animals, though they were not structurally identified.
- The study was initially performed using Uptisphere Strategy NEC as the chromatographic column.
- Later, after observing the increased use of new chromatographic supports like hydrophilic interaction chromatography for analyzing polar compounds in metabolomics studies, the researchers investigated the usage of Uptisphere HDO and Luna hydrophilic interaction chromatography stationary phases.
- The team analyzed urinary metabolomics fingerprints to establish comparative results with the Uptisphere Strategy NEC.
Findings and Conclusion
- The most appropriate chromatographic column for the detection of new biomarkers of growth hormone was determined. It was then utilized to create a statistical model based on the analysis of over a hundred biological samples.
- While the abstract does not specify the most effective chromatographic column among Uptisphere Strategy NEC, Uptisphere HDO, and Luna hydrophilic interaction chromatography, it implies that a more effective strategy to detect growth hormone administration has been developed.
Cite This Article
APA
Boyard-Kieken F, Dervilly-Pinel G, Garcia P, Paris AC, Popot MA, le Bizec B, Bonnaire Y.
(2011).
Comparison of different liquid chromatography stationary phases in LC-HRMS metabolomics for the detection of recombinant growth hormone doping control.
J Sep Sci, 34(24), 3493-3501.
https://doi.org/10.1002/jssc.201100223 Publication
Researcher Affiliations
- Laboratoire des Courses Hippiques, Verrières le Buisson, France. f.boyard@lchfrance.fr
MeSH Terms
- Animals
- Chromatography, High Pressure Liquid
- Doping in Sports / prevention & control
- Female
- Horses
- Human Growth Hormone / analysis
- Human Growth Hormone / metabolism
- Male
- Mass Spectrometry
- Metabolomics / methods
- Recombinant Proteins / analysis
- Recombinant Proteins / metabolism
Citations
This article has been cited 6 times.- Patterson Rosa L, Mallicote MF, Long MT, Brooks SA. Metabogenomics reveals four candidate regions involved in the pathophysiology of Equine Metabolic Syndrome. Mol Cell Probes 2020 Oct;53:101620.
- Ghaste M, Mistrik R, Shulaev V. Applications of Fourier Transform Ion Cyclotron Resonance (FT-ICR) and Orbitrap Based High Resolution Mass Spectrometry in Metabolomics and Lipidomics. Int J Mol Sci 2016 May 25;17(6).
- Melanie S, Benedikt K, Pfaffl MW, Irmgard R. The potential of circulating extracellular small RNAs (smexRNA) in veterinary diagnostics-Identifying biomarker signatures by multivariate data analysis. Biomol Detect Quantif 2015 Sep;5:15-22.
- Kiss A, Lucio M, Fildier A, Buisson C, Schmitt-Kopplin P, Cren-Olivé C. Doping control using high and ultra-high resolution mass spectrometry based non-targeted metabolomics-a case study of salbutamol and budesonide abuse. PLoS One 2013;8(9):e74584.
- Duntas LH, Popovic V. Hormones as doping in sports. Endocrine 2013 Apr;43(2):303-13.
- Barboni D, Bozza D, Spadafora DN, Bianchi N, Myftari B, Tedeschi P, De Luca C, Felletti S, Spedicato M, Cavazzini A, Catani M. Comparative evaluation of reversed-phase and hydrophilic interaction liquid chromatography columns for untargeted profiling of bioactive compounds in Hypericum perforatum. Anal Bioanal Chem 2026 Jan;418(2):687-699.
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