Literature DB >> 2023109

Moment analysis of drug disposition in kidney. V: In vivo transepithelial transport of p-aminohippurate in rat kidney.

R Hori1, Y L He, Y Saito, A Kamiya, Y Tanigawara.   

Abstract

A new method that can assess the kinetics of in vivo transepithelial transport in rat kidney has been established. The method is based upon a multiple-indicator dilution experiment and the moment analysis theory. After simultaneous bolus injections of p-aminohippurate (PAH) and inulin into the right renal artery, blood samples were taken from the carotid artery and urine was separately collected from right and left ureters. The characteristic response for the first passage of drugs through the right kidney was evaluated by taking blood circulation into consideration. To determine the mean artery-to-vein transit time and the extraction ratio in the kidney, an intravenous injection was also performed as a reference experiment for deconvolution. The urinary excretion curve corresponding to the first passage was obtained as the difference between both kidneys. The mean artery-to-lumen transit time (mean transepithelial transit time, Tcell) was computed by subtracting the mean urinary transit time of inulin from that of secreted PAH. Since transport across the luminal membrane into the lumen from tubular epithelial cells can influence the cellular residence time of drugs, Tcell and the single-pass mean residence time in epithelial cells (Tcell,sp) can be thought of describing luminal membrane transport. The value of Tcell obtained for 0.1 mM PAH was 22 sec and it was prolonged to 61 sec in the presence of probenecid, suggesting an inhibitory effect on transport across the luminal membrane. On the other hand, antiluminal membrane transport into cells from blood is characterized by the volume of distribution in the kidney (VdPAH). VdPAH was remarkably decreased by treatment with probenecid, indicating an inhibitory effect on antiluminal membrane transport. The effects of probenecid on both sides of epithelial cell membrane transport were first demonstrated in vivo. The present method is useful for the analysis of in vivo transepithelial transport including antiluminal and luminal membrane transport for drugs excreted via tubular secretion.

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Year:  1991        PMID: 2023109     DOI: 10.1007/bf01062192

Source DB:  PubMed          Journal:  J Pharmacokinet Biopharm        ISSN: 0090-466X


  34 in total

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Authors:  E C Foulkes
Journal:  Am J Physiol       Date:  1977-05

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Authors:  C A Goresky; W H Ziegler; G G Bach
Journal:  Circ Res       Date:  1970-11       Impact factor: 17.367

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Journal:  Pflugers Arch       Date:  1969       Impact factor: 3.657

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Authors:  J E Lewy; E E Windhager
Journal:  Am J Physiol       Date:  1968-05

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

6.  Statistical moments in pharmacokinetics.

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

7.  Moment analysis of drug disposition in kidney: transcellular transport kinetics of p-aminohippurate in the isolated perfused rat kidney.

Authors:  R Hori; Y Tanigawara; Y Saito; Y Hayashi; T Aiba; K Okumura; A Kamiya
Journal:  J Pharm Sci       Date:  1988-06       Impact factor: 3.534

8.  Mechanisms of p-aminohippurate transport by brush-border and basolateral membrane vesicles isolated from rat kidney cortex.

Authors:  R Hori; M Takano; T Okano; S Kitazawa; K Inui
Journal:  Biochim Biophys Acta       Date:  1982-10-22

9.  Inhibitory effect of diethyl pyrocarbonate on the H+/organic cation antiport system in rat renal brush-border membranes.

Authors:  R Hori; H Maegawa; M Kato; T Katsura; K Inui
Journal:  J Biol Chem       Date:  1989-07-25       Impact factor: 5.157

10.  Luminal and antiluminal transport of glutamine in dog kidney: effect of metabolic acidosis.

Authors:  M Silverman; P Vinay; L Shinobu; A Gougoux; G Lemieux
Journal:  Kidney Int       Date:  1981-09       Impact factor: 10.612

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  4 in total

1.  Discrepancies in pharmacokinetic parameter estimation between bolus and infusion studies in the perfused rat hindlimb.

Authors:  A C Heatherington; M Rowland
Journal:  J Pharmacokinet Biopharm       Date:  1995-10

2.  Quantitative analysis of drug handling by the kidney using a physiological model of renal drug clearance.

Authors:  I Janků; K Zvára
Journal:  Eur J Clin Pharmacol       Date:  1993       Impact factor: 2.953

3.  Effects of fosfomycin and imipenem/cilastatin on nephrotoxicity and renal excretion of vancomycin in rats.

Authors:  T Nakamura; Y Hashimoto; T Kokuryo; K I Inui
Journal:  Pharm Res       Date:  1998-05       Impact factor: 4.200

4.  Moment analysis of drug disposition in kidney. VI: Assessment of in vivo transmembrane transport of p-aminohippurate in tubular epithelium.

Authors:  Y L He; Y Tanigawara; A Kamiya; R Hori
Journal:  J Pharmacokinet Biopharm       Date:  1991-12
  4 in total

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