Abstract
Hypertension and renal dysfunction can be programmed in the rat by prenatal exposure to a lowprotein (LP) diet. Expression of the renal thick ascending limb (TAL) sodium transporter NKCC2 is up-regulated, which has been predicted to result in greater sodium reabsorption. However, we have shown that LP rats excrete more not less sodium. The aim of this study was to determine whether the increased abundance of sodium: Potassium:chloride (Na+:K+:2Cl-) co-transporter (NKCC2) leads to enhanced sodium uptake by the TAL. Pregnant Wistar rats were fed a control (18%) or LP (9%) diet. Amiloride (AM), bendroflumethiazide (BF), and furosemide (FUR) were administered acutely to male offspring at 4 weeks of age. Fractional excretion of sodium (FENa) was significantly greater in vehicle-infused LP rats (3.0±0.3%) compared with controls (1.7±0.5, P
Original language | English |
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Pages (from-to) | 285-293 |
Number of pages | 8 |
Journal | Pediatric Nephrology |
Volume | 27 |
Issue number | 2 |
DOIs | |
Publication status | Published - Feb 2012 |
Keywords
- Bendroflumethiazide
- Furosemide
- Kidney
- NKCC2
- Pressure natriuresis
- Programmed hypertension
- Sodium