Regulation of Atrial Natriuretic Peptide Secretion by α 1-adrenergic Receptors: The Role of Different Second Messenger Pathways

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A critical problem in determining the intracellular mechanisms regulating atrial natriuretic peptide (ANP) secretion is the extrapolation of data obtained in cultures of atrial myocytes isolated from neonatal animals to that obtained in intact atria isolated from adult animals. We have therefore examined ANP secretory responses in primary cultures of atrial myocytes isolated from adult rats to more closely approach the adult phenotype. Activation of α 1-adrenergic receptors by norepinephrine (in the presence of propranolol) increased the rate of ANP secretion approximately two-fold (EC 50 = 0.32 μM). This response was mediated predominately by the α 1A-like subtype of α 1-receptors. Phorbol esters increased the rate of ANP secretion approximately 2.4-fold independently of α 1-receptor occupancy. Kinetic analysis showed that the secretory responses to either agonist did not appear to diminish within 2 h. The responses to both α 1-adrenergic stimulation and phorbol ester addition were inhibited by the protein kinase C inhibitor, H-7, but not by structurally related isoquinolines. Influx of extracellular CA 2+, independently of its effects on contraction of the myocytes, was also necessary for a full secretory response to α 1-receptor activation. Additionally, the secretory response to α 1-adrenergic agonists was attenuated by calmodulin inhibitors. In contrast to the response to α 1-adrenergic receptor activation, stimulation of β-adrenergic receptors or addition of a membrane permeable cAMP analog reduced the rate of both basal and α 1-stimulated ANP secretion. These results show that activation of α 1-adrenergic receptors in adult rat atrial myocytes directly increases the rate of ANP secretion. This response is dependent upon protein kinase C and supported extracellular Ca 2+ influx. Conversely, activation of β-adrenergic receptors, which increases intracellular cAMP, directly inhibits ANP secretion.