Hypertension, Vol 15, 204-209, Copyright © 1990 by American Heart Association
T Li and BG Zimmerman
Experiments were conducted to compare the relative importance of the local
renin-angiotensin systems in the rabbit renal and femoral vascular beds and
their functional role in hemodynamic regulation. Angiotensin I (Ang I)
(0.15 microgram/kg i.v.) elevated mean arterial blood pressure by 18 +/- 1
mm Hg in the renal experimental group and 19 +/- 1 mm Hg in the femoral
experimental group; it decreased renal blood flow by 35 +/- 3% but
increased femoral blood flow by 31 +/- 8%. All these effects were blocked
by intravenous administration of captopril (2 mg/kg bolus injection plus 1
mg/kg/hr). Captopril also lowered mean arterial pressure by 17 +/- 3 and 16
+/- 2 mm Hg in the renal and femoral experimental groups, respectively, and
it increased renal blood flow by 32 +/- 10% but reduced femoral blood flow
by 21 +/- 4%. As a result, renal vascular resistance was decreased by 36
+/- 5%, but femoral vascular resistance remained unchanged. After
captopril, plasma angiotensin II (Ang II) levels were decreased and Ang I
levels increased in the two groups. The renal venous-arterial difference of
Ang I was increased by captopril, but the femoral venous-arterial
difference of Ang I was not, suggesting greater generation of Ang I in the
kidney. In a separate group of bilateral nephrectomized rabbits, plasma Ang
II levels as well as mean arterial pressure, femoral blood flow, and
femoral vascular resistance were not changed by intravenous administration
of captopril.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
In vivo comparison of renal and femoral vascular sensitivity and local angiotensin generation
Department of Pharmacology, University of Minnesota, Minneapolis 55455.
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