Abstract
CGP 28,014 is a specific inhibitor of catechol-O-methyltransferase (COMT) in vivo. In humans, the inhibition was assessed by measuring urinary excretion of isoquinolines and with the levodopa test. Following administration of CGP 28,014, urinary excretion of isoquinolines was significantly increased. In rats, CGP 28,014 reduced plasma and striatal concentrations of 3-O-methyldopa (30MD) in a dose-dependent manner. Acute and subchronic administration of CGP 28,014 alone or in combination with the peripherally acting decarboxylase inhibitor benserazide decreased plasma 30MD as an index of COMT inhibition by about 50%. There seems to be a close relationship between the time-course of plasma concentrations of CGP 28,014 and the extent of COMT inhibition assessed by the 30MD/DOPA ratio in plasma.
MeSH terms
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Amidines / administration & dosage
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Amidines / pharmacokinetics
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Amidines / pharmacology*
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Animals
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Benserazide / pharmacology
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Catechol O-Methyltransferase Inhibitors*
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Corpus Striatum / drug effects
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Corpus Striatum / metabolism
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Dopamine / urine
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Dose-Response Relationship, Drug
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Homovanillic Acid / urine
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Humans
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Isoquinolines / urine
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Kinetics
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Methoxyhydroxyphenylglycol / urine
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Norepinephrine / urine
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Pyridones / administration & dosage
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Pyridones / pharmacokinetics
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Pyridones / pharmacology*
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Rats
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Tyrosine / analogs & derivatives
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Tyrosine / blood
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Tyrosine / metabolism
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Vanilmandelic Acid / urine
Substances
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Amidines
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Catechol O-Methyltransferase Inhibitors
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Isoquinolines
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Pyridones
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N-(2-pyridone-6-yl)-N',N'-di-n-propylformamidine
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Tyrosine
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1,2-dehydrosalsolinol
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Methoxyhydroxyphenylglycol
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Vanilmandelic Acid
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Benserazide
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salsolinol
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3-methoxytyrosine
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Dopamine
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Norepinephrine
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Homovanillic Acid