Literature DB >> 1438005

Effect of chronic administration of phenobarbital on the hepatobiliary transport of phenol red: assessment by statistical moment analysis.

T Kakutani1, K Endo, E Nara, S Nakazora, M Hashida.   

Abstract

The effect of enzyme induction on the hepatobiliary transport of phenol red (PR) in rats was investigated by application of a new analytical system to determine local drug disposition based on statistical moment theory (T. Kakutani et al., J. Pharmacokin. Biopharm. 13:609-631, 1985). Employing the moment parameters obtained from the time courses of plasma and biliary concentrations of PR and its metabolite after intravenous injection, the hepatobiliary transport of PR was theoretically assessed by separating it into component subprocesses such as hepatic uptake, hepatobiliary transfer, and intrahepatic metabolism. The results demonstrated that the acceleration of plasma disappearance of PR caused by pretreatment with phenobarbital (PB), known to induce hepatic enzyme systems, could be attributed to elevation of both hepatic and extrahepatic clearances. While PB did cause bile flow elevation (choleresis) and increased metabolism, these effects were shown to make little contribution to accelerated plasma disappearance of PR, since it was shown that the hepatobiliary excretion of PR was rate-limited by the intrahepatic transfer process, which was unaffected by PB treatment. From the results of this study, this experimental/analysis methodology seems to be useful in obtaining detailed information about hepatobiliary transport of the drug from in vivo data.

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Year:  1992        PMID: 1438005     DOI: 10.1023/a:1015852916524

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  29 in total

1.  Statistical moments and disposition parameters in a local perfusion system under mammillary nonequilibrium condition.

Authors:  T Kakutani; E Nara; M Hashida
Journal:  J Pharmacokinet Biopharm       Date:  1990-10

2.  Substrate-selective induction of rabbit hepatic UDP-glucuronyltransferases by ethanol and other xenobiotics.

Authors:  B L Finley; P J Ashley; A G Neptune; G S Yost
Journal:  Biochem Pharmacol       Date:  1986-09-01       Impact factor: 5.858

3.  Influence of phenobarbital on factors responsible for hepatic clearance of indocyanine green in the rat: relative contributions of induction and altered liver blood flow.

Authors:  D G McDevitt; A S Nies; G R Wilkinson
Journal:  Biochem Pharmacol       Date:  1977-07-01       Impact factor: 5.858

4.  Effects of microsomal enzyme inducers on carrier-mediated transport systems in isolated rat hepatocytes.

Authors:  D L Eaton; C D Klaassen
Journal:  J Pharmacol Exp Ther       Date:  1979-03       Impact factor: 4.030

5.  A new method for assessment of drug disposition in muscle: application of statistical moment theory to local perfusion systems.

Authors:  T Kakutani; K Yamaoka; M Hashida; H Sezaki
Journal:  J Pharmacokinet Biopharm       Date:  1985-12

Review 6.  Renal organic anion transport system: pharmacological, physiological, and biochemical aspects.

Authors:  J V Møller; M I Sheikh
Journal:  Pharmacol Rev       Date:  1982-12       Impact factor: 25.468

7.  Hemodynamic influences upon the variance of disposition residence time distribution of drugs.

Authors:  M Weiss
Journal:  J Pharmacokinet Biopharm       Date:  1983-02

8.  Importance of hepatic function on the plasma disappearance and biliary excretion of hexachlorophene.

Authors:  C D Klaassen
Journal:  Toxicol Appl Pharmacol       Date:  1979-06-15       Impact factor: 4.219

9.  Influence of acute renal failure on pharmacokinetics of phenolsulfonphthalein in rats: a comparative study in vivo and in the simultaneous perfusion system of liver and kidney.

Authors:  M Yasuhara; H Katayama; J Fujiwara; K Okumura; R Hori
Journal:  J Pharmacobiodyn       Date:  1985-05

10.  Relation between renal and hepatic excretion of drugs: I. Phenol red in comparison with p-aminohippurate and indocyanine green.

Authors:  C Fleck; H Bräunlich
Journal:  Exp Pathol       Date:  1986
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  1 in total

1.  New hepatocellular diffusion model for analysis of hepatobiliary transport processes of drugs.

Authors:  H Yasui; K Yamaoka; T Nakagawa
Journal:  J Pharmacokinet Biopharm       Date:  1995-04
  1 in total

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