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Kinetic study on p-tyramine metabolism in humans using stable isotope-labeled tracers

Neurochemical Research

Jun 1, 1993

M ShimamuraH Naruse

PMID: 8510798

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Abstract

A sensitive method for the determination of p-tyramine was developed using gas chromatography-chemical ionization mass spectrometry. This method was combined with a stable isotope tracer technique to study p-tyramine metabolism in humans. [2H]5-Phenylalanine was administered orally to m...read more

Mentioned in this Paper

Metabolic Process, Cellular
Urine
Mass Spectrometry
Tyramine
Body Excretions
Metabolic Pathway
Excretory Function
para-Tyramine
Chromatography, Gas-Liquid
Deuterons
Paper Details
References
  • References7
  • Citations1

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Kinetic study on p-tyramine metabolism in humans using stable isotope-labeled tracers

Neurochemical Research

Jun 1, 1993

M ShimamuraH Naruse

PMID: 8510798

DOI:

Abstract

A sensitive method for the determination of p-tyramine was developed using gas chromatography-chemical ionization mass spectrometry. This method was combined with a stable isotope tracer technique to study p-tyramine metabolism in humans. [2H]5-Phenylalanine was administered orally to m...read more

Mentioned in this Paper

Metabolic Process, Cellular
Urine
Mass Spectrometry
Tyramine
Body Excretions
Metabolic Pathway
Excretory Function
para-Tyramine
Chromatography, Gas-Liquid
Deuterons

Feeds With Similar Papers

Phenylketonuria

Phenylketonuria (PKU) is an inborn error of metabolism that results from a deficiency of phenylalanine hydroxylase (PAH). Discover the latest research on phenylketonuria here.

Related Papers

Biological Trace Element Research

Selenium and rubidium changes in subjects with pathologically altered thyroid

Biological Trace Element ResearchJanuary 1, 1992
J KvícalaV Zeman
Paper Details
References
  • References7
  • Citations1

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