Importance of Residual Water Permeability on the Excretion of Water during Water Diuresis in Rats
- PMID: 21468191
- PMCID: PMC3041495
- DOI: 10.5049/EBP.2010.8.1.1
Importance of Residual Water Permeability on the Excretion of Water during Water Diuresis in Rats
Abstract
When the concentration of sodium (Na(+)) in arterial plasma (P(Na)) declines sufficiently to inhibit the release of vasopressin, water will be excreted promptly when the vast majority of aquaporin 2 water channels (AQP2) have been removed from luminal membranes of late distal nephron segments. In this setting, the volume of filtrate delivered distally sets the upper limit on the magnitude of the water diuresis. Since there is an unknown volume of water reabsorbed in the late distal nephron, our objective was to provide a quantitative assessment of this parameter. Accordingly, rats were given a large oral water load, while minimizing non-osmotic stimuli for the release of vasopressin. The composition of plasma and urine were measured. The renal papilla was excised during the water diuresis to assess the osmotic driving force for water reabsorption in the inner medullary collecting duct. During water diuresis, the concentration of creatinine in the urine was 13-fold higher than in plasma, which implies that ~8% of filtered water was excreted. The papillary interstitial osmolality was 600 mOsm/L > the urine osmolality. Since 17% of filtered water is delivered to the earliest distal convoluted tubule micropuncture site, we conclude that half of the water delivered to the late distal nephron is reabsorbed downstream during water diuresis. The enormous osmotic driving force for the reabsorption of water in the inner medullary collecting duct may play a role in this reabsorption of water. Possible clinical implications are illustrated in the discussion of a case example.
Keywords: basal water permeability; desalination; polyuria; vasopressin.
Figures



References
-
- Robertson GL. The Kidney. 4th ed. v.1. New York: Raven press; 2008. Thirst and vasopressin; pp. 1123–1142.
-
- Nielsen S, Frokiaer J, Marples D, Kwon TH, Agre P, Knepper MA. Aquaporins in the kidney: from molecules to medicine. Physiol Rev. 2002;82:205–244. - PubMed
-
- Halperin ML, Kamel KS, Oh MS. Mechanisms to concentrate the urine: an opinion. Curr Opin Nephrol Hypertens. 2008;17:416–422. - PubMed
-
- Shafiee MA, Charest AF, Cheema-Dhadli S, et al. Defining conditions that lead to the retention of water: the importance of the arterial sodium concentration. Kidney Int. 2005;67:613–621. - PubMed
-
- Lankford SP, Chou CL, Terada Y, Wall SM, Wade JB, Knepper MA. Regulation of collecting duct water permeability independent of cAMP-mediated AVP response. Am J Physiol. 1991;261:F554–F566. - PubMed