Quantitation of 3,4-dihydroxyphenylacetaldehyde and 3, 4-dihydroxyphenylglycolaldehyde, the monoamine oxidase metabolites of dopamine and noradrenaline, in human tissues by microcolumn high-performance liquid chromatography
- PMID: 10452806
- DOI: 10.1006/abio.1999.4196
Quantitation of 3,4-dihydroxyphenylacetaldehyde and 3, 4-dihydroxyphenylglycolaldehyde, the monoamine oxidase metabolites of dopamine and noradrenaline, in human tissues by microcolumn high-performance liquid chromatography
Abstract
We recently described the chemical synthesis of 3, 4-dihydroxyphenylacetaldehyde and 3,4-dihydroxyphenylglycolaldehyde, the monamine oxidase metabolites of dopamine and noradrenaline, respectively. We demonstrated the neurotoxicity of these compounds. Catecholamine nerve cells which synthesize these aldehydes die in degenerative brain diseases, such as Parkinson's and Alzheimer's. Here we describe a sensitive method for separating these catecholaldehydes from catecholamines and their other oxidative and methylated metabolites by microcolumn high-performance liquid chromatography with electrochemical detection. We then quantitate catecholamines and their major metabolites in human brain, plasma, and urine. The method can be used to determine the role of these catecholaldehydes in human disease.
Similar articles
-
Neurotoxicity of MAO metabolites of catecholamine neurotransmitters: role in neurodegenerative diseases.Neurotoxicology. 2004 Jan;25(1-2):101-15. doi: 10.1016/S0161-813X(03)00090-1. Neurotoxicology. 2004. PMID: 14697885 Review.
-
Determination of serotonin, noradrenaline, dopamine and their metabolites in rat brain extracts and microdialysis samples by column liquid chromatography with fluorescence detection following derivatization with benzylamine and 1,2-diphenylethylenediamine.J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Aug 5;807(2):177-83. doi: 10.1016/j.jchromb.2004.03.069. J Chromatogr B Analyt Technol Biomed Life Sci. 2004. PMID: 15203027
-
Differential Susceptibilities of Catecholamines to Metabolism by Monoamine Oxidases.J Pharmacol Exp Ther. 2021 Nov;379(3):253-259. doi: 10.1124/jpet.121.000826. Epub 2021 Sep 9. J Pharmacol Exp Ther. 2021. PMID: 34503991 Free PMC article.
-
The simultaneous determination of 3,4-dihydroxyphenyl-ethylene glycol, 3,4-dihydroxyphenylacetic acid and catecholamines in brain tissue by high performance liquid chromatography with electrochemical detection.Neurosci Lett. 1983 Aug 8;38(3):327-32. doi: 10.1016/0304-3940(83)90390-7. Neurosci Lett. 1983. PMID: 6415553
-
Dopamine-derived salsolinol derivatives as endogenous monoamine oxidase inhibitors: occurrence, metabolism and function in human brains.Neurotoxicology. 2004 Jan;25(1-2):193-204. doi: 10.1016/S0161-813X(03)00099-8. Neurotoxicology. 2004. PMID: 14697894 Review.
Cited by
-
Biogenic Aldehyde-Mediated Mechanisms of Toxicity in Neurodegenerative Disease.Curr Opin Toxicol. 2019 Feb;13:16-21. doi: 10.1016/j.cotox.2018.12.002. Epub 2018 Dec 17. Curr Opin Toxicol. 2019. PMID: 31304429 Free PMC article.
-
Effect of ALDH2 on Sleep Disturbances in Patients with Parkinson's Disease.Sci Rep. 2019 Dec 12;9(1):18950. doi: 10.1038/s41598-019-55427-w. Sci Rep. 2019. PMID: 31831791 Free PMC article.
-
Catecholamine autotoxicity. Implications for pharmacology and therapeutics of Parkinson disease and related disorders.Pharmacol Ther. 2014 Dec;144(3):268-82. doi: 10.1016/j.pharmthera.2014.06.006. Epub 2014 Jun 16. Pharmacol Ther. 2014. PMID: 24945828 Free PMC article. Review.
-
A model of dopamine and serotonin-kynurenine metabolism in cortisolemia: Implications for depression.PLoS Comput Biol. 2021 May 10;17(5):e1008956. doi: 10.1371/journal.pcbi.1008956. eCollection 2021 May. PLoS Comput Biol. 2021. PMID: 33970902 Free PMC article.
-
Protein reactivity of 3,4-dihydroxyphenylacetaldehyde, a toxic dopamine metabolite, is dependent on both the aldehyde and the catechol.Chem Res Toxicol. 2009 Jul;22(7):1256-63. doi: 10.1021/tx9000557. Chem Res Toxicol. 2009. PMID: 19537779 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources