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Clinical Chemistry, Vol 19, 927-936, Copyright © 1973 by the American Association for Clinical Chemistry
1 Oak Ridge National Laboratory,1 Oak Ridge, Tenn.
37830.
Urines, selected to demonstrate the utility of the LC
system known as the "UV-Analyzer" for simultaneous investigation of a wide range of metabolites,
were obtained from Parkinsonian patients being
treated with l-DOPA alone or l-DOPA plus
-methyldopahydrazine, a dopa decarboxylase inhibitor. Sulfate conjugates are the major excretion products of those metabolites of l-DOPA retaining the
catechol (3,4-dihydroxyphenyl) structure. Administration of the dopa decarboxylase inhibitor considerably decreased urinary excretion of 3,4-dihydroxyphenylacetic and 3,4-dihydroxymandelic acids and
increased excretion of 3-methoxy-4-hydroxy-phenyl
lactic acid. Urinary chromatograms obtained for several children with neurological disorders manifest by
seizures, infantile autism, and mental retardation
showed elevated excretion of 4-hydroxyphenylacetic
(a metabolite of tyramine) and 4-hydroxyhippuric
acids. Two of the more severely affected children
excreted a new metabolite, identified by mass spectrometry and gas chromatographymass spectrometry as
-methoxy-
-(3-methoxy-4-hydroxyphenyl)-acetic acid. This homolog of 3-methoxy-4-hydroxymandelic acid (VMA) was observed also in urine
samples from patients with other types of diseases,
including chronic lymphocytic leukemia, Lesch
Nyhan syndrome, malignant carcinoid, synovial sarcoma, multiple myeloma, and embryonic neoplasia.
Its metabolic precursors are unknown.
-methoxy-
-(3-methoxy-4-hydroxyphenyl)-acetic acid
(
-methoxyhomovanillic acid) anion-exchange chromatography inherited metabolic disease metabolic pathways
Submitted on May 3, 1973
Accepted on May 26, 1973
The following articles in journals at HighWire Press have cited this article:
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C. D. Scott High-Pressure Ion Exchange Chromatography Science, October 18, 1974; 186(4160): 226 - 233. [PDF] |
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