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Nitric oxide produced by endothelial nitric oxide synthase promotes diuresis

Authors :
Perez-Rojas, Jazmin M.
Kassem, Kamal M.
Beierwaltes, William H.
Garvin, Jeffrey L.
Herrera, Marcela
Source :
The American Journal of Physiology. April, 2010, Vol. 298 Issue 4, pR1050, 6 p.
Publication Year :
2010

Abstract

Perez-Rojas JM, Kassem KM, Beierwaltes WH, Garvin JL, Herrera M. Nitric oxide produced by endothelial nitric oxide synthase promotes diuresis. Am J Physiol Regul lntegr Comp Physiol 298: R1050-R1055, 2010. First published February 10, 2010; doi: 10.1152/ajpregu.00181.2009.--Exwacellular fluid volume is highly regulated, at least in part, by peripheral resistance and renal function. Nitric oxide (NO) produced by NO synthase type 3 (NOS 3) in the nonrenal vasculature may promote fluid retention by reducing systemic vascular resistance and arterial pressure. In contrast, NO produced by renal NOS 3 promotes water excretion by reducing renal vascular resistance, increasing glomerular filtration, and inhibiting reabsorption along the nephron. Thus, the net effect of NO from NOS 3 on urinary volume (UV) is unclear. We hypothesized that NO produced by NOS 3 promotes water excretion primarily due to renal tubular effects. We gave conscious wild-type and NOS 3 -/- mice an acute volume load and measured UV, blood pressure, plasma renin concentration (PRC), [Na.sup.+], vasopressin, and urinary [Na.sup.+] and creatinine concentrations. To give the acute volume load, we trained mice to drink a large volume of water while in metabolic cages. On the day of the experiment, water was replaced with 1% sucrose, and mice had access to it for 1 h. Volume intake was similar in both groups. Over 3 h, wild-type mice excreted 62 [+ or -] 10% of the volume load, but NOS 3 -/- excreted only 42 [+ or -] 5% (P < 0.05). Blood pressure in NOS 3 -/- was 118 [+ or -] 3 compared with 110 [+ or -] 2 mmHg in wild-type mice (P < 0.05), but it did not change following volume load in either strain. PRC, vasopressin, and glomerular filtration rate were similar between groups. Urinary [Na.sup.+] excretion was 49.3 [+ or -] 7.0 in wild-type vs. 37.8 [+ or -] 6.4 [micro]mol/3 h in NOS 3 -/- mice (P < 0.05). Bumetanide administration eliminated the difference in volume excretion between wild-type and NOS 3 -/- mice. We conclude that 1) NO produced by NOS 3 promotes water and [Na.sup.+] excretion and 2) the renal epithelial actions of NO produced by NOS 3 supersede the systemic and renal vascular actions. nitric oxide; nitric oxide synthase 3; diuresis; transport doi: 10.1152/ajpregu.00181.2009.

Details

Language :
English
ISSN :
00029513
Volume :
298
Issue :
4
Database :
Gale General OneFile
Journal :
The American Journal of Physiology
Publication Type :
Academic Journal
Accession number :
edsgcl.224166957