Martin B Lee1, Malina K Storer, John W Blunt, Michael Lever. 1. Biochemistry Unit, Canterbury Health Laboratories, P.O. Box 151, Christchurch, New Zealand; Department of Chemistry, University of Canterbury, Christchurch, New Zealand.
Abstract
BACKGROUND: Methylamines have many metabolic roles and there is an increasing demand for their measurement. Glycine betaine is an important osmolyte, and a reservoir for methyl groups. Proline betaine and trigonelline are important dietary betaines. Trimethylamine, derived from gut flora, is normally converted to trimethylamine oxide but in 'fish odour syndrome' is excreted as TMA. These compounds are all suitable for quantification by (1)H NMR spectroscopy as they all have methyl protons. METHOD: Urine samples are acidified and (1)H NMR spectra are obtained using presaturation for water suppression. Peak integrals or heights are compared to an internal standard of acetonitrile. RESULTS: Inter- and intra-assay CV's were <5% for TMAO and creatinine, and <10% for the other analytes. Responses were linear from 50 to 1000 microM for all metabolites, and recoveries were > or =97%. Limits of detection using NMR are slightly higher than alternative HPLC assays (15-25 microM). However, sensitivity is adequate for the detection of raised levels in urine, and sample analysis was complete in less than 5 min. CONCLUSION: (1)H NMR spectroscopy is a convenient, rapid and economical option for the determination of betaines and related compounds in urine in a single analysis.
BACKGROUND:Methylamines have many metabolic roles and there is an increasing demand for their measurement. Glycine betaine is an important osmolyte, and a reservoir for methyl groups. Proline betaine and trigonelline are important dietary betaines. Trimethylamine, derived from gut flora, is normally converted to trimethylamine oxide but in 'fish odour syndrome' is excreted as TMA. These compounds are all suitable for quantification by (1)H NMR spectroscopy as they all have methyl protons. METHOD: Urine samples are acidified and (1)H NMR spectra are obtained using presaturation for water suppression. Peak integrals or heights are compared to an internal standard of acetonitrile. RESULTS: Inter- and intra-assay CV's were <5% for TMAO and creatinine, and <10% for the other analytes. Responses were linear from 50 to 1000 microM for all metabolites, and recoveries were > or =97%. Limits of detection using NMR are slightly higher than alternative HPLC assays (15-25 microM). However, sensitivity is adequate for the detection of raised levels in urine, and sample analysis was complete in less than 5 min. CONCLUSION: (1)H NMR spectroscopy is a convenient, rapid and economical option for the determination of betaines and related compounds in urine in a single analysis.
Authors: A J Lloyd; N D Willis; T Wilson; H Zubair; E Chambers; I Garcia-Perez; L Xie; K Tailliart; M Beckmann; J C Mathers; J Draper Journal: Metabolomics Date: 2019-05-02 Impact factor: 4.290
Authors: Marek Konop; Mateusz Rybka; Emilia Waraksa; Anna K Laskowska; Artur Nowiński; Tomasz Grzywacz; Wojciech J Karwowski; Adrian Drapała; Ewa Maria Kłodzińska Journal: Int J Environ Res Public Health Date: 2021-11-23 Impact factor: 3.390