Literature DB >> 8358558

Kinetic study of the tubular dopamine outward transporter in the rat and dog kidney.

P Soares-da-Silva1.   

Abstract

1. The present study has determined the kinetic characteristics of the outflow of dopamine of renal origin in slices of rat and dog renal cortex loaded with exogenous L-dihydroxyphenylalanine (L-DOPA 5 to 5000 microM). 2. In both dog and rat renal tissues the production of dopamine was found to be dependent on the concentration of L-DOPA used and reached its maximum at 2500 microM L-DOPA. The decarboxylation of L-DOPA in rat cortical slices (16.4 +/- 2.6 to 1479.2 +/- 85.2 nmol g-1) was 6 fold that in the dog (2.2 +/- 0.4 to 252.1 +/- 21.2 nmol g-1). In the rat kidney a large amount (approximately 50%) of the dopamine (5.2 +/- 0.6 to 743.4 +/- 58.3 nmol g-1) was found to escape into the incubation medium, whereas in dog renal slices the amount of newly-formed dopamine escaping into the incubation medium (0.7 +/- 0.2 to 46.5 +/- 9.3 nmol g-1) was less than 25% of the total amount of the amine formed. 3. The application of the Michaelis-Menten equation to the net transport of newly-formed dopamine has allowed the identification of a saturable (carrier-mediated transfer) and a non-saturable component (diffusion). The Vmax (nmol g-1 15 min-1) and Km (nM) values for the saturable component were, respectively, 340 +/- 41 and 396 +/- 45 in the rat kidney and 112 +/- 16 and 319 +/- 35 in the dog kidney. In both rat and dog renal tissues, the magnitude of the non-saturable component was found to be of minor importance up to a concentration of 250 nmol g-1 of dopamine to be transported. At high concentrations of the amine (greater then 250 nmol g-1), only attainable in rat kidney slices, most of the dopamine was found to leave the compartment where the synthesis did occur through a non-saturable transport system.4. In conclusion, the results presented here show that the outflow of newly-formed dopamine in both dog and rat kidney slices loaded with exogenous L-DOPA follows Michaelis-Menten kinetics with a saturable component and a non-saturable one, the latter assuming particular importance only at higher concentrations of the amine.

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Year:  1993        PMID: 8358558      PMCID: PMC2175669          DOI: 10.1111/j.1476-5381.1993.tb13609.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  28 in total

1.  EFFECTS OF AUTONOMIC DRUGS ON RENAL TUBULAR TRANSPORT OF CATECHOLAMINES IN THE CHICKEN.

Authors:  B R RENNICK; M Z PRYOR
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Review 2.  The plasma membrane sodium-hydrogen exchanger and its role in physiological and pathophysiological processes.

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Authors:  S G Ball; N S Oats; M R Lee
Journal:  Clin Sci Mol Med       Date:  1978-08

4.  The distribution of p-aminohippuric acid in rat kidney slices. I. Tubular localization.

Authors:  R P Wedeen; B Weiner
Journal:  Kidney Int       Date:  1973-04       Impact factor: 10.612

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Authors:  C R Ross; P D Holohan
Journal:  Annu Rev Pharmacol Toxicol       Date:  1983       Impact factor: 13.820

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Authors:  A Aperia; A Bertorello; I Seri
Journal:  Am J Physiol       Date:  1987-01

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Authors:  Y L Chan
Journal:  J Pharmacol Exp Ther       Date:  1976-10       Impact factor: 4.030

8.  The renal tubular transport and metabolism of serotonin (5-HT) and 5-hydroxyindoleacetic acid (5-HIAA) in the chicken.

Authors:  R Hakim; W M Watrous; J M Fujimoto
Journal:  J Pharmacol Exp Ther       Date:  1970-12       Impact factor: 4.030

9.  Dopamine receptors modulate sodium excretion in denervated kidney.

Authors:  P A Jose; R A Felder; R R Holloway; G M Eisner
Journal:  Am J Physiol       Date:  1986-06

10.  Effects of salt intake and renal denervation on catecholamine catabolism and excretion.

Authors:  A D Baines
Journal:  Kidney Int       Date:  1982-02       Impact factor: 10.612

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  3 in total

1.  Assessment of renal dopaminergic system activity in the nitric oxide-deprived hypertensive rat model.

Authors:  P Soares-da-Silva; M Pestana; M A Vieira-Coelho; M H Fernandes; A Albino-Teixeira
Journal:  Br J Pharmacol       Date:  1995-04       Impact factor: 8.739

2.  Renal tubular dopamine outward transfer during Na(+)-H+ exchange activation by alpha 1- and alpha 2-adrenoceptor agonists.

Authors:  P Soares-da-Silva
Journal:  Br J Pharmacol       Date:  1993-06       Impact factor: 8.739

3.  The renal handling of dopamine originating from L-dopa and gamma-glutamyl-L-dopa.

Authors:  M Pestana; P Soares-da-Silva
Journal:  Br J Pharmacol       Date:  1994-06       Impact factor: 8.739

  3 in total

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