Circulation, Vol 52, 130-136, Copyright © 1975 by American Heart Association
RA Levinsky, RM Lewis, TE Bynum and HG HANLEY
Previous studies have been shown that intravenous cardiac glycosides
produce mesenteric vasoconstriction (MVC). The possibility that this might
critically compromise blood flow in patients with mesenteric vascular
disease was suggested. To evaluate whether MVC occurs with intravenous
cardiac glycosides in the presence of proximal mesenteric artery stenosis,
blood flow in the superior mesenteric artery (SMA) of thirteen dogs was
measured with a Doppler flowmeter. The SMA was constricted and pressures
were measured in the aorta, SMA, and superior mesenteric vein. Superior
mesenteric vascular resistance (SMVR) was calculated by dividing the
pressure difference between the SMA and superior mesenteric vein by the
total blood flow to the superior mesenteric vasculature and was reported as
mm Hg/cc-min. Blood flow was measured simultaneously by a drop rate meter
in the vein of a surgically isolated intestinal segment supplied by a
single arterial arcade. Venous outflow pressure from this segment was also
monitored, which allowed calculation of isolated gut segment resistance
(IGSR) in mm Hg/cc-min per 100 g gut. Stenosis of the SMA produced pressure
gradients of 10 to 75 mm Hg and decreased resting blood flow by as much as
82%. Digoxin produced an increase in both SMVR and IGSR throughout the 30
to 120 minute period of the study in thirteen dogs despite the presence of
severe grades of SMA stenosis. There was no relationship between the degree
of proximal SMA stenosis and the magnitude of resistance change due to
digoxin. To determine if this MVC was reversible, glucagon was administered
to eleven dogs 30 to 60 minutes after digoxin and completely overcame the
constriction. Thus, digoxin produced MVC in the presence of proximal SMA
stenosis. This MVC was pharmacologically reversible. These data suggest
that intravenous digoxin might contribute to intestinal ischemia in
patients with preexisting vascular disease.
ARTICLES
Digoxin induced intestinal vasoconstriction. The effects of proximal arterial stenosis and glucagon administration
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