Literature DB >> 1115054

Normal antipyrine metabolism in patients with cholesterol cholelithiasis. Evidence that the disease is not due to generalized hepatic microsomal dysfunction.

G W Hepner, E S Vesell.   

Abstract

Plasma antipyrine half-lives and metabolic clearances were measured after a single oral dose of antipyrine in 10 control subjects, 12 patients with gallstones, and 9 patients having undergone cholecystectomy for cholesterol cholelithiasis, to determine whether impairment of hepatic antipyrine metabolism occurs in patients with cholesterol cholelithiasis. The plasma antipyrine half-life and metabolic clearances in the control subjects were 11.7 plus or minus 1.3 hours and 42.5 plus or minus 3.3 ml/min, respectively; in patients with gallstones, 12.3 plus or minus 1.3 hours and 36.0 plus or minus 3.2 ml/min, respectively; and in patients having undergone cholecystectomy, 13.2 plus or minus 1.8 hours and 33.8 plus or minus 4.2 ml/min, respectively. Values for antipyrine half-life and metabolic clearance were not statistically different in these three groups. This study suggests the presence of normal hepatic antipyrine metablosim in patients with cholesterolcholelithiasis.

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Year:  1975        PMID: 1115054     DOI: 10.1007/bf01073131

Source DB:  PubMed          Journal:  Am J Dig Dis        ISSN: 0002-9211


  16 in total

1.  The estimation of antipyrine in biological materials.

Authors:  B B BRODIE; J AXELROD
Journal:  J Biol Chem       Date:  1949-05       Impact factor: 5.157

2.  The effect of spironolactone on antipyrine metabolism in man.

Authors:  D H Huffman; D W Shoeman; P Pentikäinen; D L Azarnoff
Journal:  Pharmacology       Date:  1973       Impact factor: 2.547

Review 3.  Hepatic synthesis of bile acids. Biochemical steps and mechanisms of rate control.

Authors:  E H Mosbach
Journal:  Arch Intern Med       Date:  1972-10

4.  [The determination of cholesterol 7 -hydroxylase activity in rat liver].

Authors:  D Mayer; F W Koss; A Glasenapp
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1972-06

Review 5.  The biological synthesis of cholesterol.

Authors:  K Bloch
Journal:  Science       Date:  1965-10-01       Impact factor: 47.728

6.  Genetic control of drug levels in man: antipyrine.

Authors:  E S Vesell; J G Page
Journal:  Science       Date:  1968-07-05       Impact factor: 47.728

7.  On the metabolism of cholesterol in rat liver homogenates. Bile acids and steroids.193.

Authors:  I Björkhem; H Danielsson; K Einarsson
Journal:  Eur J Biochem       Date:  1968-05

8.  Mechanism of hepatic drug oxidation and its relationship to individual differences in rates of oxidation in man.

Authors:  D S Davies; S S Thorgeirsson
Journal:  Ann N Y Acad Sci       Date:  1971-07-06       Impact factor: 5.691

9.  Determination of hepatic cholesterol 7alpha-hydroxylase activity in man.

Authors:  F J Schmitz; F J McDonald
Journal:  J Lipid Res       Date:  1974-03       Impact factor: 5.922

10.  Determinants of serum antipyrine half-lives in patients with liver disease.

Authors:  R A Branch; C M Herbert; A E Read
Journal:  Gut       Date:  1973-07       Impact factor: 23.059

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  4 in total

1.  The effect of phenobarbital on biliary lipid metabolism and hepatic microsomal drug metabolism in patients with cholesterol cholelithiasis.

Authors:  G W Hepner
Journal:  Am J Dig Dis       Date:  1976-05

2.  Further observations on relationships between antipyrine half-life, clearance and volume of distribution: an appraisal of alternative kinetic parameters used to assess the elimination of antipyrine.

Authors:  L G Sultatos; B H Dvorchik; E S Vesell; D G Shand; R A Branch
Journal:  Clin Pharmacokinet       Date:  1980 May-Jun       Impact factor: 6.447

3.  Pharmacokinetics of phenazone (antipyrine) in rabbits with experimental common bile duct obstruction.

Authors:  J Wójcicki; T Sulikowski; M Wójcicki; M Droździk; B Gawrońska-Szklarz; B Barcew-Wiszniewska; J Skowron; L Rózewicka
Journal:  Br J Pharmacol       Date:  1996-01       Impact factor: 8.739

4.  Pharmacokinetics of lidocaine and its major metabolite- monoethylglycinexylidide (MEGX) in rabbits with experimental common bile duct obstruction.

Authors:  J Wójcicki; T Sulikowski; M Wójcicki; M Droździk; B Gawrońska-Szklarz; B Barcew-Wiszniewska; J Skowron; L Rózewicka; U Gołdyn
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1995 Apr-Jun       Impact factor: 2.441

  4 in total

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