TY - JOUR
T1 - Adrenergic mechanisms of catecholamine action on glucose homeostasis in man
AU - Rizza, R. A.
AU - Cryer, P. E.
AU - Haymond, M. W.
AU - Gerich, J. E.
N1 - Funding Information:
From the Endocrine Research Unii. Departments of Medicine and Physiology. Mayo Medical School and Ma.yo Clinic, Rochester, Minn. and the Metabolism Division. Washington ffniversity School of Medicine,S t, Louis. MO. Supported in part by USPHS grants AM00648, AM2041 1. AM20837, AM05827. RR00585. AM20579, and RR0036 and by grants from the Diabetic Children’s Welfare Association/American Diabetes Association, Greater St. Louis Afiliate. and the Mayo Foundation, Rochester, Minn. Dr. Rizza is a recipient of a Clinical Investigator Award from the National Institutes of Arthritis and Metabolic Diseases. Address reprint requests io Dr. R. A. R&a. Endocrine Research Unit, Mayo Clinic. Rochester, Minn. 55901, @I 980 by Grune & Stratton, Inc. 0026~495/80/2913~009$01.00/0
PY - 1980
Y1 - 1980
N2 - To assess the adrenergic mechanisms responsible for the effect of epinephrine on glucose production and glucose clearance in man, epinephrine (50 ng/kg/min) was infused in the presence and absence of alpha adrenergic (phentolamine) and beta adrenergic (propranolol) antagonists under conditions when plasma glucose, insulin, and glucagon levels were allowed to vary and when they were clamped by a concurrent infusion of glucose, somatostatin, and insulin. When plasma glucose, insulin, and glucagon were permitted to vary during beta adrenergic blockade, plasma glucose and glucose production increased, respectively, 32% and 42% less and plasma epinephrine concentrations were threefold greater than those during infusion of epinephrine alone; plasma insulin decreased during beta blockade but increased during infusion of epinephrine alone; glucose clearance was comparably suppressed in both instances. When alpha adrenergic blockade was superimposed on beta blockade, the increase in glucose production and the decrease in both plasma insulin and glucose clearance observed during infusion of epinephrine alone was virtually abolished. In contrast, when plasma glucose, insulin, and glucagon were clamped, beta adrenergic blockade completely prevented the suppression of glucose clearance by epinephrine and inhibited the stimulation of glucose production by epinephrine by 80% whereas alpha adrenergic blockade had no effect on either of these parameters. These results indicate that in man, epinephrine increases glucose production and decreases glucose clearance by both alpha and beta adrenergic actions. The alpha adrenergic effects could be accounted for by inhibition of insulin secretion. The mechanism for the beta adrenergic effects remains to be defined but may reflect a direct action of epinephrine on hepatic and peripheral tissues.
AB - To assess the adrenergic mechanisms responsible for the effect of epinephrine on glucose production and glucose clearance in man, epinephrine (50 ng/kg/min) was infused in the presence and absence of alpha adrenergic (phentolamine) and beta adrenergic (propranolol) antagonists under conditions when plasma glucose, insulin, and glucagon levels were allowed to vary and when they were clamped by a concurrent infusion of glucose, somatostatin, and insulin. When plasma glucose, insulin, and glucagon were permitted to vary during beta adrenergic blockade, plasma glucose and glucose production increased, respectively, 32% and 42% less and plasma epinephrine concentrations were threefold greater than those during infusion of epinephrine alone; plasma insulin decreased during beta blockade but increased during infusion of epinephrine alone; glucose clearance was comparably suppressed in both instances. When alpha adrenergic blockade was superimposed on beta blockade, the increase in glucose production and the decrease in both plasma insulin and glucose clearance observed during infusion of epinephrine alone was virtually abolished. In contrast, when plasma glucose, insulin, and glucagon were clamped, beta adrenergic blockade completely prevented the suppression of glucose clearance by epinephrine and inhibited the stimulation of glucose production by epinephrine by 80% whereas alpha adrenergic blockade had no effect on either of these parameters. These results indicate that in man, epinephrine increases glucose production and decreases glucose clearance by both alpha and beta adrenergic actions. The alpha adrenergic effects could be accounted for by inhibition of insulin secretion. The mechanism for the beta adrenergic effects remains to be defined but may reflect a direct action of epinephrine on hepatic and peripheral tissues.
UR - http://www.scopus.com/inward/record.url?scp=0019275583&partnerID=8YFLogxK
U2 - 10.1016/0026-0495(80)90025-6
DO - 10.1016/0026-0495(80)90025-6
M3 - Article
C2 - 7001182
AN - SCOPUS:0019275583
SN - 0026-0495
VL - 29
SP - 1155
EP - 1163
JO - Metabolism: clinical and experimental
JF - Metabolism: clinical and experimental
IS - 11
ER -