Abstract

The effect of catecholamines (epinephrine, norepinephrine, isoproterenol, and phenylephrine) on cyclic adenosine 3′:5′-monophosphate (cAMP) level in isolated catfish ( Ictalurus melas) liver cells was studied in the presence or absence of α (phentolamine) and β (propranolol)-receptor antagonists. All catecholamines increased the hepatocyte cAMP level; the rank of their potency was epinephrine = isoproterenol > norepinephrine > phenylephrine. Propranolol completely blocked the catecholamine effect; phentolamine was ineffective. Results confirm previous findings ( L. Brighenti, A. C. Puviani, M. E. Gavioli, and C. Ottolenghi, 1987, Gen. Comp. Endocrinol. 66, 306–313) that epinephrine and norepinephrine act via β-receptor activation. However, the comparison of the effects of isoproterenol and phenylephrine on cAMP with those on phosphorylase a and on glycogen breakdown suggests that a more complex mechanism is possibly involved in the catecholamine effect on catfish glycogenolysis.

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