Literature DB >> 6146267

Age-dependent renal effects of intrarenal dopamine infusion.

J C Pelayo, R D Fildes, P A Jose.   

Abstract

Three groups of anesthetized puppies 16.4 +/- 1.2 (group I), 29.6 +/- 1.6 (group II), and 49.8 +/- 2.5 (group III) days of age were used to assess the renal response to graded doses of dopamine infusion into the renal artery. Dopamine infusion at 1 microgram X kg-1 X min-1 increased renal blood flow (RBF) from 3.61 +/- 0.31 to 4.22 +/- 0.43 ml X min-1 X g kidney wet wt-1 (P less than 0.05) only in the older puppies (group III). Glomerular filtration rate (GFR) increased in groups II and III from control values of 0.69 +/- 0.14 and 0.61 +/- 0.08 to 1.08 +/- 0.19 and 0.83 +/- 0.05 ml X min-1 X g kidney wet wt-1, respectively (P less than 0.05). However, urinary flow rate and sodium excretion were variably affected. Because dopamine is known to stimulate both alpha- and beta-adrenoceptors in addition to dopamine receptors, two additional groups of puppies 11.2 +/- 1.2 (group IV) and 72.8 +/- 2.4 (group V) days of age were studied to evaluate the renal effects of dopamine during the continuous intrarenal infusion of phentolamine and nadolol (an alpha- and a beta-adrenergic blocker, respectively). Dopamine elicited increases in RBF only in the older puppies (P less than 0.05). GFR, urinary flow rate, and sodium excretion increased in both groups; however, the magnitude of the change was greater for each parameter in the older group (P less than 0.05). These experiments suggest a maturational process for specific dopamine receptors and/or effector response, which may affect the observed age-dependent increases in RBF, GFR, and renal sodium handling.

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Year:  1984        PMID: 6146267     DOI: 10.1152/ajpregu.1984.247.1.R212

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  7 in total

Review 1.  Mechanisms regulating renal sodium excretion during development.

Authors:  J E Robillard; F G Smith; J L Segar; E N Guillery; P A Jose
Journal:  Pediatr Nephrol       Date:  1992-03       Impact factor: 3.714

Review 2.  Molecular biology of adrenergic and dopamine receptors and the study of developmental nephrology.

Authors:  P A Jose; R A Felder; C C Felder; W Y Chan
Journal:  Pediatr Nephrol       Date:  1990-11       Impact factor: 3.714

3.  Loss of NHERF-1 expression prevents dopamine-mediated Na-K-ATPase regulation in renal proximal tubule cells from rat models of hypertension: aged F344 rats and spontaneously hypertensive rats.

Authors:  Michelle T Barati; Corey J Ketchem; Michael L Merchant; Walter B Kusiak; Pedro A Jose; Edward J Weinman; Amanda J LeBlanc; Eleanor D Lederer; Syed J Khundmiri
Journal:  Am J Physiol Cell Physiol       Date:  2017-05-17       Impact factor: 4.249

4.  Effects of low-dose dopamine on urine output in normotensive very low birth weight neonates.

Authors:  J L Crouchley; P B Smith; C M Cotten; C D Hornik; R N Goldberg; J W Foreman; J L Wynn
Journal:  J Perinatol       Date:  2013-02-28       Impact factor: 2.521

5.  Effect of low-dose dopamine infusion on urinary prostaglandin E2 excretion in sick, preterm infants.

Authors:  I Seri; J Hajdu; J Kiszel; T Tulassay; A Aperia
Journal:  Eur J Pediatr       Date:  1988-08       Impact factor: 3.183

Review 6.  Dopamine, kidney, and hypertension: studies in dopamine receptor knockout mice.

Authors:  Xiaoyan Wang; Van Anthony M Villar; Ines Armando; Gilbert M Eisner; Robin A Felder; Pedro A Jose
Journal:  Pediatr Nephrol       Date:  2008-07-10       Impact factor: 3.714

7.  Dopamine receptors in the developing sheep kidney.

Authors:  R A Felder; K T Nakamura; J E Robillard; M Kanadjian; P A Jose
Journal:  Pediatr Nephrol       Date:  1988-01       Impact factor: 3.714

  7 in total

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