PT  - JOURNAL ARTICLE
AU  - Rafael F. Schäfers
AU  - Jens Nürnberger
AU  - Burghard Herrmann
AU  - Rene R. Wenzel
AU  - Thomas Philipp
AU  - Martin C. Michel
TI  - Adrenoceptors Mediating the Cardiovascular and Metabolic Effects of α-Methylnoradrenaline in Humans
DP  - 1999 May 01
TA  - Journal of Pharmacology and Experimental Therapeutics
PG  - 918--925
VI  - 289
IP  - 2
4099  - http://jpet.aspetjournals.org/content/289/2/918.short
4100  - http://jpet.aspetjournals.org/content/289/2/918.full
SO  - J Pharmacol Exp Ther1999 May 01; 289
AB  - α-Methylnoradrenaline is a widely used tool to study α2-adrenoceptor function, but its selectivity for this receptor has not been validated in humans in vivo. To characterize the adrenoceptors mediating cardiovascular and metabolic effects of α-methylnoradrenaline in humans, we have performed graded i.v. infusions of α-methylnoradrenaline in a randomized, placebo-controlled crossover study in six young, healthy males in the absence and presence of the β-adrenoceptor antagonist propranolol, the α1-adrenoceptor antagonist doxazosin, and the α2-adrenoceptor antagonist yohimbine. α-Methylnoradrenaline dose-dependently increased heart rate, systolic blood pressure, cardiac output, blood glucose, serum insulin, free fatty acids, and gastrin, shortened the duration of heart rate-corrected electromechanical systole, and decreased diastolic blood pressure, total peripheral resistance, and plasma noradrenaline. Propranolol completely reversed the rise in heart rate and cardiac output, the fall in peripheral resistance, the shortening of electromechanical systole, and the rise in insulin; it blunted the increase in free fatty acids and gastrin. Yohimbine did not significantly influence most parameters but significantly potentiated the rise in insulin, blunted the increase in glucose, and prevented the fall in noradrenaline. Doxazosin was largely without effect on any of these parameters. We conclude that i.v. administered α-methylnoradrenaline primarily acts on β-adrenoceptors in the human cardiovascular and metabolic system, but an α2-adrenergic component of the response is detectable for changes of plasma noradrenaline, blood glucose, and serum insulin. Whereas α-methylnoradrenaline is selective for α2- over α1-adrenoceptors, β-adrenoceptor blockade is required to unmask α-adrenoceptor-mediated vasoconstriction. The American Society for Pharmacology and Experimental Therapeutics