Abstract
Summary
In confirmation of other studies, SC injection of glucagon increased exhaled CO2 (apparent metabolic rate) of rats. Contrary to expectation, SC and IP injection of glucagon did not increase exhaled CO2 of mice. Glucagon did, however, produce expected loss of liver glycogen and hyperglycemia in mice. Subcutaneous injection of epinephrine increased exhaled CO2 of both rats and mice.
Glucagon appeared to increase oxidation rate of C14-glycerol and decrease oxidation of C14-palmitic acid; opposite effects were obtained with epinephrine. The “glucagon effect”on C14-glycerol oxidation was brief and dependent on initial utilization of C14-glycerol, as fasting mice with greater oxidation rates did not respond. This oxidative stimulation was not dependent on hyperglycemia per se, adrenal hormones or insulin.
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