Literature DB >> 4786541

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

R D Hughes, P Millburn, R T Williams.   

Abstract

1. The excretion in the bile and urine of intraperitoneally injected (14)C-labelled monoquaternary ammonium or pyridinium cations was measured in bile-duct-cannulated rats (ten compounds) and in guinea pigs and rabbits (six compounds). 2. Seven of these, namely N-methylpyridinium, tetraethylammonium, trimethylphenylammonium, diethylmethylphenylammonium, methylphenyldipropylammonium, dibenzyldimethylammonium and tribenzylmethylammonium, were excreted largely unchanged in the bile and urine. 3. 3-Hydroxyphenyltrimethylammonium, 3-bromo-N-methylpyridinium and cetyltrimethylammonium were metabolized to an appreciable extent in the rat. 4. In intact rats intraperitoneally injected trimethylphenylammonium (mol.wt. 136) was excreted mainly in the urine, dibenzyldimethylammonium (mol.wt. 226) was excreted in roughly equal amounts in the urine and faeces, and tribenzylmethylammonium (mol.wt. 302) was excreted mainly in the faeces. The faecal excretion of these compounds corresponded to their biliary excretion in bile-duct-cannulated rats. About 3-4% of tribenzyl[(14)C]methylammonium was eliminated as (14)CO(2). 5. In rats the extent of biliary excretion of four cations with molecular weights in the range 94-164 was less than 10% of the dose, whereas that of five cations with molecular weights 173-302 was greater than 10%. These results and other data from the literature suggested that the molecular weight needed for the biliary excretion of such cations to an extent of 10% or more of the dose was about 200+/-50. Studies with six cations in guinea pigs and rabbits suggest that this value applies also to these species. 6. The results suggest that the threshold molecular weight for the appreciable (>10%) biliary excretion of monoquaternary cations is different from that for anions (Millburn et al., 1967a; Hirom et al., 1972b). With rats, guinea pigs and rabbits, no significant species difference was noted, whereas with anions there is a marked species difference.

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Year:  1973        PMID: 4786541      PMCID: PMC1166046          DOI: 10.1042/bj1360967

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


  20 in total

1.  Active transport of quaternary ammonium compounds into bile.

Authors:  L S SCHANKER; H M SOLOMON
Journal:  Am J Physiol       Date:  1963-05

2.  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

3.  Metabolism and biliary excretion of phenanthridinium salts. I. Nature of the biliary metabolites.

Authors:  J T MacGregor; T W Clarkson
Journal:  Biochem Pharmacol       Date:  1971-10       Impact factor: 5.858

4.  Disposition of bretylium in man and rat. A sensitive chemical method for its estimation in plasma and urine.

Authors:  R Kuntzman; I Tsai; R Chang; A H Conney
Journal:  Clin Pharmacol Ther       Date:  1970 Nov-Dec       Impact factor: 6.875

5.  Distribution, excretion and metabolism of prifinium bromide.

Authors:  T Nakai; H Noguchi; M Okui; K Tada
Journal:  Arzneimittelforschung       Date:  1970-08

6.  The fate of (14C)phenol in various species.

Authors:  I D Capel; M R French; P Millburn; R L Smith; R T Williams
Journal:  Xenobiotica       Date:  1972-01       Impact factor: 1.908

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.  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

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  11 in total

1.  Different activity of ATP dependent transport across the canalicular membrane for tributylmethylammonium and triethylmethylammonium as a potential mechanism of the preferential biliary excretion for tributylmethylammonium in the rat.

Authors:  I S Song; S J Chung; C K Shim
Journal:  Pharm Res       Date:  1999-04       Impact factor: 4.200

Review 2.  Enterohepatic circulation: physiological, pharmacokinetic and clinical implications.

Authors:  Michael S Roberts; Beatrice M Magnusson; Frank J Burczynski; Michael Weiss
Journal:  Clin Pharmacokinet       Date:  2002       Impact factor: 6.447

Review 3.  Carrier-mediated transport in the hepatic distribution and elimination of drugs, with special reference to the category of organic cations.

Authors:  D K Meijer; W E Mol; M Müller; G Kurz
Journal:  J Pharmacokinet Biopharm       Date:  1990-02

4.  Structure-pharmacokinetics relationship of quaternary ammonium compounds. Elimination and distribution characteristics.

Authors:  C Neef; R Oosting; D K Meijer
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1984-12       Impact factor: 3.000

5.  Increased affinity to canalicular P-gp via formation of lipophilic ion-pair complexes with endogenous bile salts is associated with mw threshold in hepatobiliary excretion of quaternary ammonium compounds.

Authors:  Im-Sook Song; Min-Koo Choi; Qing-Ri Jin; Won-Sik Shim; Chang-Koo Shim
Journal:  Pharm Res       Date:  2010-03-10       Impact factor: 4.200

6.  Prediction of biliary excretion in rats and humans using molecular weight and quantitative structure-pharmacokinetic relationships.

Authors:  Xinning Yang; Yash A Gandhi; David B Duignan; Marilyn E Morris
Journal:  AAPS J       Date:  2009-07-11       Impact factor: 4.009

7.  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

8.  Contribution of ion-pair complexation with bile salts to the transport of organic cations across LLC-PK1 cell monolayers.

Authors:  Im-Sook Song; Yong-Hae Han; Suk-Jae Chung; Chang-Koo Shim
Journal:  Pharm Res       Date:  2003-04       Impact factor: 4.200

9.  Tissue distribution kinetics of tetraethylammonium ion in the rat.

Authors:  M Mintun; K J Himmelstein; R L Schroder; M Gibaldi; D D Shen
Journal:  J Pharmacokinet Biopharm       Date:  1980-08

10.  Structure-pharmacokinetics relationship of quaternary ammonium compounds. Correlation of physicochemical and pharmacokinetic parameters.

Authors:  C Neef; D K Meijer
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1984-12       Impact factor: 3.000

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