Literature DB >> 4647268

Renal handling of phenol red. I. A comparative study on the accumulation of phenol red and p-aminohippurate in rabbit kidney tubules in vitro.

M I Sheikh.   

Abstract

1. The characteristics of renal accumulation of phenol red and p-aminohippurate (PAH) by slices of rabbit kidney cortex suspended in an electrolyte medium have been compared.2. It has been found that at low medium concentrations the accumulation of phenol red is about 4-5 times as high as that of PAH. Furthermore, phenol red is accumulated by the renal tissue under anaerobic conditions, in contrast to PAH.3. Experiments involving incubation of slices at low temperatures and addition of various metabolic inhibitors to the medium, indicate that the anaerobic accumulation of phenol red is due to binding to cellular constituents. This conclusion is corroborated by studies on renal homogenates from which it appears that phenol red is bound predominantly to the microsomal and mitochondrial fraction.4. The aerobic accumulation of phenol red is less susceptible to inhibition by probenecid, 2,4-dinitrophenol (DNP), and octanoate than is that of PAH. Besides, probenecid, DNP, and octanoate inhibit phenol red binding to the microsomal fraction, whereas mitochondrial binding of phenol red is unaffected by the presence of these substances.5. Fumarate and succinate affect the aerobic accumulation of phenol red and PAH to the same degree. Furthermore, fumarate, succinate, and PAH do not alter anaerobic accumulation of phenol red.6. It is concluded that probenecid, DNP, and octanoate cause more inhibition of organic anion transport than fumarate, succinate, and PAH because of lipophilic interaction with the membrane. The pronounced resistance of phenol red accumulation to inhibition by lipophilic inhibitors is probably due to the ability of the indicator dye to displace these substances from binding sites on the transporting membranes.

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Year:  1972        PMID: 4647268      PMCID: PMC1331211          DOI: 10.1113/jphysiol.1972.sp010048

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  39 in total

1.  Oxygen consumption and active transport in separated renal tubules.

Authors:  M B BURG; J ORLOFF
Journal:  Am J Physiol       Date:  1962-08

2.  On the mechanism of action of probenecid on renal tubular secretion.

Authors:  I M WEINER; J A WASHINGTON; G H MUDGE
Journal:  Bull Johns Hopkins Hosp       Date:  1960-06

3.  Localization of nephron transport by stop flow analysis.

Authors:  R L MALVIN; W S WILDE; L P SULLIVAN
Journal:  Am J Physiol       Date:  1958-07

4.  Tissue fractionation studies. 6. Intracellular distribution patterns of enzymes in rat-liver tissue.

Authors:  C DE DUVE; B C PRESSMAN; R GIANETTO; R WATTIAUX; F APPELMANS
Journal:  Biochem J       Date:  1955-08       Impact factor: 3.857

5.  THE MEASUREMENT OF THE TUBULAR EXCRETORY MASS, EFFECTIVE BLOOD FLOW AND FILTRATION RATE IN THE NORMAL HUMAN KIDNEY.

Authors:  H W Smith; W Goldring; H Chasis
Journal:  J Clin Invest       Date:  1938-05       Impact factor: 14.808

6.  Metabolic studies on renal transport of p-aminohippurate in vitro.

Authors:  J Maxild; J V Moller
Journal:  Biochim Biophys Acta       Date:  1969-09-02

7.  Role of fatty acid metabolism on renal transport of p-aminohippurate in vitro.

Authors:  J Maxild
Journal:  Biochim Biophys Acta       Date:  1971-04-13

8.  Probenecid uptake by slices of rabbit kidney cortex.

Authors:  W O Berndt
Journal:  Biochem Pharmacol       Date:  1966-12       Impact factor: 5.858

9.  The relation between secretion of urate and p-aminohippurate in the rabbit kidney.

Authors:  J V Moller
Journal:  J Physiol       Date:  1967-09       Impact factor: 5.182

10.  The fuel of respiration of rat kidney cortex.

Authors:  M J Weidemann; H A Krebs
Journal:  Biochem J       Date:  1969-04       Impact factor: 3.857

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  8 in total

1.  Renal handling of phenol red. II. The mechanism of substituted phenolsulphophthalein (PSP) dye transport in rabbit kidney tubules in vitro.

Authors:  M I Sheikh
Journal:  J Physiol       Date:  1976-03       Impact factor: 5.182

2.  Renal handling of phenol red. III. Bidirectional transport.

Authors:  U Gerdes; J Kristensen; J V Møller; M I Sheikh
Journal:  J Physiol       Date:  1978-04       Impact factor: 5.182

3.  Serine uptake by luminal and basolateral membrane vesicles from rabbit kidney.

Authors:  U Kragh-Hansen; M I Sheikh
Journal:  J Physiol       Date:  1984-09       Impact factor: 5.182

4.  Physiologically based pharmacokinetic model for the renal clearance of phenolsulfonphthalein and the interaction with probenecid and salicyluric acid in the dog.

Authors:  F G Russel; A C Wouterse; C A van Ginneken
Journal:  J Pharmacokinet Biopharm       Date:  1987-08

5.  An efficient method for the isolation and separation of basolateral-membrane and luminal-membrane vesicles from rabbit kidney cortex.

Authors:  M I Sheikh; U Kragh-Hansen; K E Jørgensen; H Røigaard-Petersen
Journal:  Biochem J       Date:  1982-11-15       Impact factor: 3.857

6.  The use of a potential-sensitive cyanine dye for studying ion-dependent electrogenic renal transport of organic solutes. Uptake of L-malate and D-malate by luminal-membrane vesicles.

Authors:  U Kragh-Hansen; K E Jørgensen; M I Sheikh
Journal:  Biochem J       Date:  1982-11-15       Impact factor: 3.857

7.  Renal transport of neutral amino acids. Tubular localization of Na+-dependent phenylalanine- and glucose-transport systems.

Authors:  U Kragh-Hansen; H Røigaard-Petersen; C Jacobsen; M I Sheikh
Journal:  Biochem J       Date:  1984-05-15       Impact factor: 3.857

8.  Expression levels of renal organic anion transporters (OATs) and their correlation with anionic drug excretion in patients with renal diseases.

Authors:  Yuji Sakurai; Hideyuki Motohashi; Harumasa Ueo; Satohiro Masuda; Hideyuki Saito; Masahiro Okuda; Noriko Mori; Motokazu Matsuura; Toshio Doi; Atsushi Fukatsu; Osamu Ogawa; Ken-ichi Inui
Journal:  Pharm Res       Date:  2004-01       Impact factor: 4.200

  8 in total

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