Abstract
Antipyrine has been used as a model drug to investigate the effects of liver disease on drug metabolism in man. A prolongation in antipyrine half-life (T(1/2)) was found in patients with liver disease, patients with chronic liver disease showing a greater increase than those with acute, reversible pathology. The most marked prolongation in T(1/2) was found in association with hypoalbuminaemia and hypoprothrombinaemia, suggesting that the cause for these changes was defective protein synthesis of microsomal enzyme protein. This hypothesis was supported by demonstrating that enzyme-inducing agents, which are known to increase the amount of microsomal enzyme protein, reduced the antipyrine half-life.
MeSH Terms
Adult
Alkaline Phosphatase/blood
Antipyrine/blood,metabolism
Aspartate Aminotransferases/blood
Bilirubin/blood
Half-Life
Hepatitis/blood
Humans
Hypoproteinemia/blood
Hypoprothrombinemias/blood
Liver Cirrhosis/blood
Liver Diseases/blood
Liver Function Tests
Microsomes, Liver/enzymology
Middle Aged
Phenobarbital
Prednisone
Prothrombin/analysis
Serum Albumin/analysis
Chemicals
Serum Albumin
Prothrombin
Aspartate Aminotransferases
Alkaline Phosphatase
Bilirubin
Antipyrine
Prednisone
Phenobarbital
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Branch R A
Herbert C M
Read A E
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