Hypertension, Vol 22, 847-852, Copyright © 1993 by American Heart Association
NJ Brown, D Ryder and J Nadeau
Non-modulation has been proposed as an intermediate phenotype in human
essential hypertension. The trait is characterized by blunted aldosterone
and renal plasma flow responses to short-term angiotensin II (Ang II)
infusion. Elevated tissue Ang II levels or decreased tissue adenosine
levels could account for this decreased sensitivity to Ang II. In support
of the latter possibility, endogenous adenosine has been shown to
contribute to the renal vasoconstrictive response to Ang II in animals. We
therefore tested the hypothesis that endogenous adenosine contributes to
modulation of renal plasma flow in sodium-replete humans. We examined the
effect of long-term administration of the adenosine receptor antagonist
caffeine on baseline renal plasma flow and on the renal plasma flow
response to short-term Ang II infusion in six salt-replete normotensive
subjects in a single-blind, placebo- controlled study. para-Aminohippurate
clearance was used to assess renal plasma flow. Ang II was infused in
graded doses (0.3 to 3 ng/kg per minute) in the presence and absence of
caffeine (250 mg PO TID for 7 days). Blood pressure, plasma renin activity,
Ang II, electrolytes, and para-aminohippurate clearance were measured
before and after each dose of Ang II. Caffeine did not alter either
baseline blood pressure or the blood pressure response to Ang II but did
increase baseline plasma renin activity from 0.72 +/- 0.09 to 1.42 +/- 0.26
ng angiotensin I/mL per hour (P = .01).(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Caffeine attenuates the renal vascular response to angiotensin II infusion
Vanderbilt University Medical Center, Division of Clinical Pharmacology, Nashville, TN.
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