Literature DB >> 743252

Biliary excretion of cyclohexylphenyl 4-[35S]sulphate in the guinea pig.

G M Powell, A H Olavesen, C G Curtis.   

Abstract

The metabolic fate and mode of excretion of cyclohexylphenyl 4-[35S]sulphate were studied in the guinea pig. Up to 54.8% of the dose appeared in the bile, the majority as unchanged ester. Substantial amounts of hydroxylated cyclohexylphenyl 4-[35S]sulphate were also excreted in the bile together with minor amounts of the corresponding glucuronic acid conjugate. When isolated guinea-pig livers were perfused with cyclohexylphenyl 4-[35S]sulphate the biliary components were the same as those in the intact animal, although the relative concentration of the hydroxylated derivative was significantly greater. When the hydroxylated derivative was re-injected into guinea pigs it was excreted almost entirely unchanged in the bile. However, in the rat, it was excreted in the bile as a glucuronic acid conjugate. These findings are discussed in relation to studies carried out in the rat [Hearse, Powell, Olavesen & Dodgson (1969) Biochem. Pharmacol. 18, 181--195] and to differences in enzyme activities in rat and guinea-pig liver. The results are also discussed in terms of the molecular-weight threshold for the excretion of anions in guinea-pig bile.

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Year:  1978        PMID: 743252      PMCID: PMC1186252          DOI: 10.1042/bj1760443

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  9 in total

1.  Observations on the metabolism of tyrosine O[35S]-sulphate in the rat.

Authors:  K S DODGSON; G M POWELL; F A ROSE; N TUDBALL
Journal:  Biochem J       Date:  1961-05       Impact factor: 3.857

2.  Metabolic fates of diethylstilboestrol sulphates in the rat.

Authors:  P A Barford; A H Olavesen; C G Curtis; G M Powell
Journal:  Biochem J       Date:  1977-05-15       Impact factor: 3.857

3.  The biliary excretion of tartrazine. Sex differences in the rat and species differences in the rat, guinea-pig and rabbit.

Authors:  R H Gregson; P C Hirom; P Millburn; R L Smith; H B Turbert; R T Williams
Journal:  J Pharm Pharmacol       Date:  1972-01       Impact factor: 3.765

4.  Sex and species differences in the biliary excretion of tartrazine and lissamine fast yellow in the rat, guinea-pig and rabbit. The influence of sex hormones on tartrazine excretion in the rat.

Authors:  P Bertagni; P C Hirom; P Millburn; F O Osiyemi; R L Smith; H B Turbert; R T Williams
Journal:  J Pharm Pharmacol       Date:  1972-08       Impact factor: 3.765

5.  The influence of some physico-chemical factors on the biliary excretion of a series of structurally related aryl sulphate esters.

Authors:  D J Hearse; G M Powell; A H Olavesen; K S Dodgson
Journal:  Biochem Pharmacol       Date:  1969-01       Impact factor: 5.858

6.  The preparation and characterization of a series of 35S-labelled aryl sulphate esters for metabolic studies.

Authors:  D J Hearse; A H Olavesen; G M Powell
Journal:  Biochem Pharmacol       Date:  1969-01       Impact factor: 5.858

7.  Species variations in the threshold molecular-weight factor for the biliary excretion of organic anions.

Authors:  P C Hirom; P Millburn; R L Smith; R T Williams
Journal:  Biochem J       Date:  1972-10       Impact factor: 3.857

8.  BIOSYNTHESIS OF L-TYROSINE O-SULPHATE FROM THE METHYL AND ETHYL ESTERS OF L-TYROSINE.

Authors:  J G JONES; K S DODGSON
Journal:  Biochem J       Date:  1965-02       Impact factor: 3.857

9.  Biliary excretion of some anionic derivatives of diethylstilboestrol and phenolphthalein in the guinea pig.

Authors:  P A Barford; A H Olavesen; C G Curtis; G M Powell
Journal:  Biochem J       Date:  1977-12-15       Impact factor: 3.857

  9 in total

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