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Atrial Natriuretic Peptide and Renal Dopaminergic System: a Positive Friendly Relationship?

Overview
Journal Biomed Res Int
Publisher Wiley
Date 2014 Jul 12
PMID 25013796
Citations 4
Authors
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Abstract

Sodium metabolism by the kidney is accomplished by an intricate interaction between signals from extrarenal and intrarenal sources and between antinatriuretic and natriuretic factors. Renal dopamine plays a central role in this interactive network. The natriuretic hormones, such as the atrial natriuretic peptide, mediate some of their effects by affecting the renal dopaminergic system. Renal dopaminergic tonus can be modulated at different steps of dopamine metabolism (synthesis, uptake, release, catabolism, and receptor sensitization) which can be regulated by the atrial natriuretic peptide. At tubular level, dopamine and atrial natriuretic peptide act together in a concerted manner to promote sodium excretion, especially through the overinhibition of Na+, K+-ATPase activity. In this way, different pathological scenarios where renal sodium excretion is dysregulated, as in nephrotic syndrome or hypertension, are associated with impaired action of renal dopamine and/or atrial natriuretic peptide, or as a result of impaired interaction between these two natriuretic systems. The aim of this review is to update and comment on the most recent evidences demonstrating how the renal dopaminergic system interacts with atrial natriuretic peptide to control renal physiology and blood pressure through different regulatory pathways.

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References
1.
Wagner C, Lang F, Broer S . Function and structure of heterodimeric amino acid transporters. Am J Physiol Cell Physiol. 2001; 281(4):C1077-93. DOI: 10.1152/ajpcell.2001.281.4.C1077. View

2.
Zolty E, Ibnou-Zekri N, Izui S, Feraille E, Favre H . Glomerulonephritis and sodium retention: enhancement of Na+/K+-ATPase activity in the collecting duct is shared by rats with puromycin induced nephrotic syndrome and mice with spontaneous lupus-like glomerulonephritis. Nephrol Dial Transplant. 1999; 14(9):2192-5. DOI: 10.1093/ndt/14.9.2192. View

3.
Citarella M, Choi M, Gironacci M, Medici C, Correa A, Fernandez B . Urodilatin and dopamine: a new interaction in the kidney. Regul Pept. 2008; 153(1-3):19-24. DOI: 10.1016/j.regpep.2008.11.009. View

4.
Webb R, Della Puca R, Manniello J, ROBSON R, Zimmerman M, Ghai R . Dopaminergic mediation of the diuretic and natriuretic effects of ANF in the rat. Life Sci. 1986; 38(25):2319-27. DOI: 10.1016/0024-3205(86)90639-9. View

5.
Zhang M, Yao B, Wang S, Fan X, Wu G, Yang H . Intrarenal dopamine deficiency leads to hypertension and decreased longevity in mice. J Clin Invest. 2011; 121(7):2845-54. PMC: 3223841. DOI: 10.1172/JCI57324. View