Literature DB >> 3072557

Renal transport of drugs: an overview of methodology with application to cimetidine.

K M Giacomini1, P H Hsyu, L G Gisclon.   

Abstract

The development of new methods to study transport processes in renal epithelia has greatly enhanced our knowledge of the mechanisms involved in the transport of a number of endogenous compounds. More recently, these methods have been applied to study mechanisms of specific drug transport. This article is intended to provide an overview of the various methods used to study renal elimination of compounds. References to more detailed reviews of the individual methods are provided. Studies of the renal transport of cimetidine, a histamine H2-receptor antagonist, are presented to illustrate the application of these methods to the study of specific drugs. Methods such as clearance techniques and the Sperber chicken preparation used to study renal elimination of compounds in whole animals are briefly described. Techniques to identify the site of renal transport including stop flow, isolated perfused tubules, and micropuncture methods are discussed and references to more technical reviews are cited. The more recently developed methods of isolated membrane vesicles for studying transport across the individual polar membranes of the proximal tubule are discussed along with the relevant studies of the use of these membranes in elucidating the mechanisms involved in the renal transport of cimetidine. Finally, the use of cultured renal epithelial cell lines in studying renal transport is described. Knowledge of drug transport mechanisms in the kidney is important both in drug targeting to the kidney and in understanding the pharmacokinetics of renally eliminated drugs. As exemplified by the studies with cimetidine, only by combining the data from experiments using diverse methodology can the mechanisms involved in the renal excretion of compounds be delineated.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1988        PMID: 3072557     DOI: 10.1023/a:1015904905235

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


  39 in total

1.  Isolated membrane vesicles in the evaluation of the nature, localization, and regulation of renal transport processes.

Authors:  R Kinne; I L Schwartz
Journal:  Kidney Int       Date:  1978-12       Impact factor: 10.612

Review 2.  Micropuncture techniques.

Authors:  G A Quamme; J H Dirks
Journal:  Kidney Int       Date:  1986-08       Impact factor: 10.612

Review 3.  Transport studies in plasma membrane vesicles isolated from renal cortex.

Authors:  H Murer; P Gmaj
Journal:  Kidney Int       Date:  1986-08       Impact factor: 10.612

4.  Accumulation of cimetidine by kidney cortex slices.

Authors:  W Cacini; M B Keller; V R Grund
Journal:  J Pharmacol Exp Ther       Date:  1982-05       Impact factor: 4.030

5.  Mechanisms of organic cation transport in kidney plasma membrane vesicles: 2. delta pH studies.

Authors:  P D Holohan; C R Ross
Journal:  J Pharmacol Exp Ther       Date:  1981-02       Impact factor: 4.030

6.  Cimetidine transport in rat renal brush border and basolateral membrane vesicles.

Authors:  M Takano; K Inui; T Okano; R Hori
Journal:  Life Sci       Date:  1985-10-28       Impact factor: 5.037

Review 7.  Clinical pharmacokinetics of cimetidine.

Authors:  A Somogyi; R Gugler
Journal:  Clin Pharmacokinet       Date:  1983 Nov-Dec       Impact factor: 6.447

8.  Retention of differentiated characteristics by cultures of defined rabbit kidney epithelia.

Authors:  P D Wilson; R J Anderson; R D Breckon; W Nathrath; R W Schrier
Journal:  J Cell Physiol       Date:  1987-02       Impact factor: 6.384

9.  Renal excretion of cimetidine.

Authors:  I M Weiner; L Roth
Journal:  J Pharmacol Exp Ther       Date:  1981-03       Impact factor: 4.030

10.  Cimetidine inhibits renal procainamide clearance.

Authors:  C D Christian; C G Meredith; K V Speeg
Journal:  Clin Pharmacol Ther       Date:  1984-08       Impact factor: 6.875

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  1 in total

1.  Altered flecainide disposition in healthy volunteers taking quinine.

Authors:  A Munafo; G Reymond-Michel; J Biollaz
Journal:  Eur J Clin Pharmacol       Date:  1990       Impact factor: 2.953

  1 in total

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