(Hypertension. 2001;37:733.)
© 2001 American Heart Association, Inc.
Scientific Contributions |
From the Medical College of Georgia and University of Mississippi Medical Center.
Correspondence to Michael W. Brands, PhD, Department of Physiology, Medical College of Georgia, 1120 15th St, Augusta, GA 30912-3000. E-mail mbrands{at}mail.mcg.edu
A
series of studies has shown that long-term infusion of insulin
and glucose does not increase mean arterial pressure (MAP)
in dogs, but we have shown that the same infusion protocol or infusion
of glucose alone increases arterial pressure in rats. This
study tested the hypothesis that infusing glucose alone in dogs, with
all insulin derived from endogenous secretion, would
increase arterial pressure. Because fructose feeding in
dogs also has been shown not to cause hypertension and because we have
shown that prostaglandin production increases
during insulin and glucose infusion, this study also tested whether
prostaglandins prevent the pressor response in dogs. Dogs
were instrumented and assigned in random crossover design to long-term
cyclooxygenase-2 (COX-2) inhibition. After baseline
measurements, glucose was infused in all dogs for 6 days (
500 g/d
IV). Plasma insulin increased 3- to 4-fold and blood glucose increased
significantly in both groups. The MAP (measured 24 h/d) response in
control dogs was variable but on average tended to increase,
although not significantly. In the dogs with COX-2 inhibition, however,
MAP increased significantly to a peak of 9±2 mm Hg and an
average of 6±1 mm Hg above control. There was significant sodium
and volume retention during glucose infusion and a significant increase
in glomerular filtration rate, but there were no
between-group differences. Plasma renin activity increased only in the
control group. This is the first study to report a long-term pressor
response with glucose infusion and hyperinsulinemia
in dogs, and it suggests that the inability to detect this relationship
previously was due to prostaglandins.
Key Words: insulin hypertension prostaglandins COX-2 renin-angiotensin
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