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Vol. 298, Issue 3, 1154-1160, September 2001
The Cardiac Physiology Laboratory, Divisions of Circulatory
Physiology and Cardiology, Department of Medicine, Columbia University,
New York, New York
Renal failure is common in heart failure due to renovascular
constriction and hypotension. We tested whether selective
pharmacological renal artery vasodilation and active renal artery
perfusion (ARP) could improve renal function without adverse effects on
systemic blood pressure in a canine model of acute heart failure (AHF). AHF was induced by coronary microembolization in 16 adult mongrel dogs.
In five dogs, selective intrarenal (IR) papaverine (1, 2, and 4 mg/min)
was administered into the left renal artery. In six dogs, ARP was
performed in the left renal artery to normalize mean renal arterial
pressure followed by administration of IR papaverine (2 mg/min). In
five dogs, ARP plus intravenous furosemide was tested. Urine output
(UO) and cortical renal blood flow decreased during AHF and were
restored by 2 mg/min IR papaverine (UO: baseline 4.2 ± 0.6, AHF
1.6 ± 1.3, IR papaverine 5.8 ± 1.1 ml/15 min; cortical blood flow: baseline 4.3 ± 0.2, AHF 2.4 ± 0.6, IR
papaverine 4.2 ± 1.2 ml/min/g) with no significant change in
aortic pressure. ARP also increased urine output and cortical renal
blood flow (UO: baseline 5.0 ± 1.1, AHF 0.5 ± 0.4, ARP
3.8 ± 3.1 ml/15 min; cortical blood flow: baseline 4.0 ± 0.5, AHF 2.0 ± 0.8, ARP 3.52 ± 1.1 ml/min/g). A combination
of these methods in AHF further increased urine output to twice the
normal baseline (10.5 ± 7.5 ml/15 min). Addition of furosemide
synergistically increased UO above that achieved with ARP alone
(5.5 ± 2.6 versus 40.3 ± 24.7 ml/15 min,
p = 0.03). In conclusion, ARP and selective renal
vasodilation may effectively promote salt and water excretion in the
setting of heart failure, particularly when systemic blood pressure is low.
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