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(Hypertension. 1999;33:937-942.)
© 1999 American Heart Association, Inc.

Scientific Contributions

A Large Blood Pressure–Raising Effect of Nitric Oxide Synthase Inhibition in Humans

Mikael Sander; Bahman Chavoshan; Ronald G. Victor

From the Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Tex.

Correspondence to Ronald G. Victor, MD, Hypertension Division, Department of Internal Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75235-8586. E-mail rvicto{at}mednet.swmed.edu

Abstract—In experimental animals, systemic administration of nitric oxide synthase (NOS) inhibitors causes large increases in blood pressure that are in part sympathetically mediated. The aim of this study was to determine the extent to which these conclusions can be extrapolated to humans. In healthy normotensive humans, we measured blood pressure in response to two NOS inhibitors, N^G-monomethyl-L-arginine (L-NMMA) and N^G-nitro-L-arginine methyl ester (L-NAME), the latter of which recently became available for use in humans. The major new findings are 3-fold. First, L-NAME produced robust increases in blood pressure that were more than 2 times larger than those previously reported in humans with L-NMMA and approximated those seen in experimental animals. L-NAME (4 mg/kg) raised mean arterial pressure by 24±2 mm Hg (n=27, P<0.001), whereas in subjects who received both inhibitors, a 12-fold higher dose of L-NMMA (50 mg/kg) raised mean arterial pressure by 15±2 mm Hg (n=4, P<0.05 vs L-NAME). Second, the L-NAME–induced increases in blood pressure were caused specifically by NOS inhibition because they were reversed by L-arginine (200 mg/kg, n=12) but not D-arginine (200 mg/kg, n=6) and because N^G-nitro-D-arginine methyl ester (4 mg/kg, n=5) had no effect on blood pressure. Third, in humans, there is an important sympathetic component to the blood pressure–raising effect of NOS inhibition. -Adrenergic blockade with phentolamine (0.2 mg/kg, n=9) attenuated the L-NAME–induced increase in blood pressure by 40% (P<0.05). From these data, we conclude that pharmacological inhibition of NOS causes large increases in blood pressure that are in part sympathetically mediated in humans as well as experimental animals.

Key Words: nitric oxide • blood pressure • L-NMMA • L-NAME • D-NAME • arginine • adrenergic receptor blockers

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