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Departments of Physiology and Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, Wisconsin 53226
This study
determined the levels of adenosine in the renal medullary interstitium
using microdialysis and fluorescence HPLC techniques and examined the
role of endogenous adenosine in the control of medullary blood flow and
sodium excretion by infusing the specific adenosine receptor
antagonists or agonists into the renal medulla of anesthetized
Sprague-Dawley rats. Renal cortical and medullary blood flows were
measured using laser-Doppler flowmetry. Analysis of microdialyzed
samples showed that the adenosine concentration in the renal medullary
interstitial dialysate averaged 212 ± 5.2 nM, which was
significantly higher than 55.6 ± 5.3 nM in the renal cortex
(n = 9). Renal medullary interstitial
infusion of a selective A1
antagonist, 8-cyclopentyl-1,3-dipropylxanthine (DPCPX; 300 pmol · kg
1 · min
1,
n = 8), did not alter renal blood
flows, but increased urine flow by 37% and sodium excretion by 42%.
In contrast, renal medullary infusion of the selective
A2 receptor blocker
3,7-dimethyl-1-propargylxanthine (DMPX; 150 pmol · kg
1 · min
1,
n = 9) decreased outer medullary blood
flow (OMBF) by 28%, inner medullary blood flows (IMBF) by 21%, and
sodium excretion by 35%. Renal medullary interstitial infusion of
adenosine produced a dose-dependent increase in OMBF, IMBF, urine flow,
and sodium excretion at doses from 3 to 300 pmol · kg
1 · min
1
(n = 7). These effects of adenosine
were markedly attenuated by the pretreatment of DMPX, but unaltered by
DPCPX. Infusion of a selective A3
receptor agonist,
N6-benzyl-5'-(N-ethylcarbonxamido)adenosine
(300 pmol · kg
1 · min
1,
n = 6) into the renal medulla had no
effect on medullary blood flows or renal function. Glomerular
filtration rate and arterial pressure were not changed by medullary
infusion of any drugs. Our results indicate that endogenous medullary
adenosine at physiological concentrations serves to dilate medullary
vessels via A2 receptors, resulting in a natriuretic response that overrides the tubular A1 receptor-mediated
antinatriuretic effects.
renal hemodynamics; renal medulla; laser-Doppler flowmetry
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