Literature DB >> 2762214

Statistical moment analysis of hepatobiliary transport of phenol red in the perfused rat liver.

K Nishida1, C Tonegawa, T Kakutani, M Hashida, H Sezaki.   

Abstract

A new experimental system was applied to study hepatobiliary transport of drugs. Rat livers were perfused using a single-pass technique, and phenol red was momentarily introduced to this system from the portal side. Outflow dilution patterns of phenol red were analyzed using statistical moment theory, and kinetic parameters of hepatic distribution and elimination of phenol red were calculated from moments, namely, the hepatic extraction ratio (Ei) and elimination rate constant (kel,i). A larger distribution volume (Vi) was obtained for phenol red than for 131I-human serum albumin (HSA) and 51Cr-red blood cells (RBC), indicating its extravascular diffusivity. The biliary excretion of conjugated phenol red was delayed relative to that of the free agent. The larger biliary mean transit time (tbile,conj.) represents the processes of biliary transport and intrahepatic metabolism. Further, the effects of dose and perfusion temperature on the hepatobiliary transport of phenol red were determined. With high doses or low perfusion temperatures (20 and 27 degrees C), Ei, kel,i, and intrinsic clearance (CLint,i) of phenol red and biliary recovery of free and conjugated phenol red (Fbile,free, Fbile,conj) significantly decreased. The temperature-dependent and saturable processes in hepatic uptake, metabolism, and biliary excretion of phenol red were assessable to moment analysis.

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Year:  1989        PMID: 2762214     DOI: 10.1023/a:1015980525940

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


  29 in total

1.  Metabolism of insulin-I 131; studies in isolated, perfused rat liver and hindlimb preparations.

Authors:  G E MORTIMORE; F TIETZE; D STETTEN
Journal:  Diabetes       Date:  1959 Jul-Aug       Impact factor: 9.461

2.  A dispersion model of hepatic elimination: 1. Formulation of the model and bolus considerations.

Authors:  M S Roberts; M Rowland
Journal:  J Pharmacokinet Biopharm       Date:  1986-06

3.  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

4.  Hepatic uptake and disposition of human polymeric IgA1 in perfused rat liver: evidence for incomplete biliary excretion and intrahepatic degradation.

Authors:  M H Finck; J Reichen; J M Vierling; T M Kloppel; W R Brown
Journal:  Am J Physiol       Date:  1985-04

5.  Disposition characteristics of lipophilic mitomycin C prodrug in an intra-arterial muscle infusion system.

Authors:  T Kakutani; Y Suematsu; W Y Cheah; E Sumimoto; M Hashida
Journal:  Chem Pharm Bull (Tokyo)       Date:  1987-12       Impact factor: 1.645

6.  In vivo determination of cellular uptake in the kidney.

Authors:  M Silverman; C Trainor
Journal:  Fed Proc       Date:  1982-12

7.  Statistical moments in pharmacokinetics.

Authors:  K Yamaoka; T Nakagawa; T Uno
Journal:  J Pharmacokinet Biopharm       Date:  1978-12

8.  Transport of dibromosulphthalein by isolated rat hepatocytes.

Authors:  A Blom; K Keulemans; D K Meijer
Journal:  Biochem Pharmacol       Date:  1981-07-01       Impact factor: 5.858

9.  Hepatic clearance of drugs. II. Experimental evidence for acceptance of the "well-stirred" model over the "parallel tube" model using lidocaine in the perfused rat liver in situ preparation.

Authors:  K S Pang; M Rowland
Journal:  J Pharmacokinet Biopharm       Date:  1977-12

10.  Albumin influences sulfobromophthalein transport by hepatocytes of each acinar zone.

Authors:  D L Gumucio; J J Gumucio; J A Wilson; C Cutter; M Krauss; R Caldwell; E Chen
Journal:  Am J Physiol       Date:  1984-01
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  8 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.  Hepatic disposition characteristics of 111In-labeled lactosaminated bovine serum albumin in rats.

Authors:  K Nishida; Y Eguchi; T Takino; Y Takakura; M Hashida; H Sezaki
Journal:  Pharm Res       Date:  1991-10       Impact factor: 4.200

3.  Disposition characteristics of plasmid DNA in the single-pass rat liver perfusion system.

Authors:  M Yoshida; R I Mahato; K Kawabata; Y Takakura; M Hashida
Journal:  Pharm Res       Date:  1996-04       Impact factor: 4.200

4.  Assessment of drug disposition in the perfused rat brain by statistical moment analysis.

Authors:  T Sakane; M Nakatsu; A Yamamoto; M Hashida; H Sezaki; S Yamashita; T Nadai
Journal:  Pharm Res       Date:  1991-06       Impact factor: 4.200

5.  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

6.  Analysis of hepatic disposition of galactosylated cationic liposome/plasmid DNA complexes in perfused rat liver.

Authors:  Shintaro Fumoto; Fumi Nakadori; Shigeru Kawakami; Makiya Nishikawa; Fumiyoshi Yamashita; Mitsuru Hashida
Journal:  Pharm Res       Date:  2003-09       Impact factor: 4.200

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

Authors:  T Kakutani; K Endo; E Nara; S Nakazora; M Hashida
Journal:  Pharm Res       Date:  1992-07       Impact factor: 4.200

8.  Pharmacokinetics and preventive effects of targeted catalase derivatives on hydrogen peroxide-induced injury in perfused rat liver.

Authors:  Yoshiyuki Yabe; Naoki Kobayashi; Makiya Nishikawa; Kiyoshi Mihara; Fumiyoshi Yamashita; Yoshinobu Takakura; Mitsuru Hashida
Journal:  Pharm Res       Date:  2002-12       Impact factor: 4.200

  8 in total

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