Literature DB >> 4656593

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

P C Hirom, P Millburn, R L Smith, R T Williams.   

Abstract

1. The excretion in the bile and urine after intravenous injection of 16 organic anions having molecular weights between 355 and 752 was studied in female rats, guinea pigs and rabbits. 2. These compounds were mostly excreted unchanged, except for three of them, which were metabolized to a slight extent (<7% of dose). 3. The rat excreted all the compounds extensively (22-90% of dose) in the bile. 4. In guinea pigs four of the compounds with mol.wt. 355-403 were excreted in the bile to the extent of 7-16% of the dose, four with mol.wt. 407-465 to the extent of 25-44% and eight compounds with mol.wt. 479-752 to the extent of 44-100%. 5. In rabbits four compounds with mol.wt. 355-465 were excreted in the bile to the extent of 1-8% of the dose, two compounds with mol.wt. 479 and 495 to the extent of 24 and 22%, and six compounds with mol.wt. 505-752 to the extent of 31-94%. 6. These results, together with those of other investigations from this laboratory, are discussed and the conclusion is reached that there is a threshold molecular weight for appreciable biliary excretion (i.e. more than 10% of dose) of anions, which varies with species: about 325+/-50 for the rat, 400+/-50 for the guinea pig and 475+/-50 for the rabbit. 7. Anions with molecular weights greater than about 500 are extensively excreted in the bile of all three species. 8. That proportion of the dose of these compounds which is not excreted in the bile is excreted in the urine, and in the three species, bile and urine are complementary excretory pathways, urinary excretion being greatest for the compounds of lowest molecular weight and tending to decrease with increasing molecular weight. 9. Some implications of this interspecies variation in the molecular-weight requirement for extensive biliary excretion are discussed.

Entities:  

Mesh:

Substances:

Year:  1972        PMID: 4656593      PMCID: PMC1174264          DOI: 10.1042/bj1291071

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


  19 in total

1.  The use of indocyanine green in the measurement of hepatic blood flow and as a test of hepatic function.

Authors:  J CAESAR; S SHALDON; L CHIANDUSSI; L GUEVARA; S SHERLOCK
Journal:  Clin Sci       Date:  1961-08       Impact factor: 6.124

2.  Studies of hepatic function with indocyanine green.

Authors:  D B HUNTON; J L BOLLMAN; H N HOFFMAN
Journal:  Gastroenterology       Date:  1960-12       Impact factor: 22.682

3.  Applications of dilution curves recorded from the right side of the heart or venous circulation with the aid of a new indicator dye.

Authors:  I J FOX; E H WOOD
Journal:  Proc Staff Meet Mayo Clin       Date:  1957-09-18

4.  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

Review 5.  The excretion of steroid hormone metabolites in bile and feces.

Authors:  W Taylor
Journal:  Vitam Horm       Date:  1971       Impact factor: 3.421

6.  Biliary excretion and enterohepatic circulation of estrone and estriol in rodents.

Authors:  A A Sandberg; R Y Kirdani; N Back; P Weyman; W R Slaunwhite
Journal:  Am J Physiol       Date:  1967-11

7.  Biliary excretion of foreign compounds. Benzene and its derivatives in the rat.

Authors:  M M Abou-El-Makarem; P Millburn; R L Smith; R T Williams
Journal:  Biochem J       Date:  1967-12       Impact factor: 3.857

8.  Biliary excretion in foreign compounds. Sulphonamide drugs in the rat.

Authors:  P Millburn; R L Smith; R T Williams
Journal:  Biochem J       Date:  1967-12       Impact factor: 3.857

9.  Biliary excretion of foreign compounds. Biphenyl, stilboestrol and phenolphthalein in the rat: molecular weight, polarity and metabolism as factors in biliary excretion.

Authors:  P Millburn; R L Smith; R T Williams
Journal:  Biochem J       Date:  1967-12       Impact factor: 3.857

10.  The role of the hepatic endoplasmic reticulum in the biliary excretion of foreign compounds by the rat. The effect of phenobarbitone and SKF 525-A (diethylaminoethyl diphenylpropylacetate).

Authors:  W G Levine; P Millburn; R L Smith; R T Williams
Journal:  Biochem Pharmacol       Date:  1970-01       Impact factor: 5.858

View more
  26 in total

1.  Physiologically based pharmacokinetic model for composite nanodevices: effect of charge and size on in vivo disposition.

Authors:  Donald E Mager; Vidhi Mody; Chao Xu; Alan Forrest; Wojciech G Lesniak; Shraddha S Nigavekar; Muhammed T Kariapper; Leah Minc; Mohamed K Khan; Lajos P Balogh
Journal:  Pharm Res       Date:  2012-06-12       Impact factor: 4.200

Review 2.  Mass balance studies, with a focus on anticancer drugs.

Authors:  Jan H Beumer; Jos H Beijnen; Jan H M Schellens
Journal:  Clin Pharmacokinet       Date:  2006       Impact factor: 6.447

3.  Estimation of biliary excretion of foreign compounds using properties of molecular structure.

Authors:  Mohsen Sharifi; Taravat Ghafourian
Journal:  AAPS J       Date:  2013-11-08       Impact factor: 4.009

4.  Kinetics of 35S-perazine in the bile fistula rat.

Authors:  U Breyer; I Jahns; G Irmscher; H Rassner; S Rehmer
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1977-10       Impact factor: 3.000

5.  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

6.  The preclinical pharmacokinetic disposition of a series of perforin-inhibitors as potential immunosuppressive agents.

Authors:  M R Bull; J A Spicer; K M Huttunen; W A Denny; A Ciccone; K A Browne; J A Trapani; N A Helsby
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2014-08-26       Impact factor: 2.441

7.  The comparative metabolism and excretion of HCE, a biodegradable analogue of dieldrin, by vertebrate species.

Authors:  C H Walker; G A El-Zorgani
Journal:  Arch Environ Contam Toxicol       Date:  1974-05       Impact factor: 2.804

8.  Biliary excretion of some diquaternary ammonium cations in the rat, guinea pig and rabbit.

Authors:  R D Hughes; P Millburn; R T Williams
Journal:  Biochem J       Date:  1973-12       Impact factor: 3.857

9.  Molecular weight as a factor in the excretion of monoquaternary ammonium cations in the bile of the rat, rabbit and guinea pig.

Authors:  R D Hughes; P Millburn; R T Williams
Journal:  Biochem J       Date:  1973-12       Impact factor: 3.857

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

Authors:  G M Powell; A H Olavesen; C G Curtis
Journal:  Biochem J       Date:  1978-11-15       Impact factor: 3.857

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.