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Evidence for Dual Adrenergic Receptor Regulation of Ovine Pineal Function
Author(s) -
Morgan P.J.,
Davidson G.R.,
Lawson W.
Publication year - 1989
Publication title -
journal of pineal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 131
eISSN - 1600-079X
pISSN - 0742-3098
DOI - 10.1111/j.1600-079x.1989.tb00665.x
Subject(s) - prazosin , receptor , endocrinology , medicine , propranolol , melatonin receptor , adrenergic receptor , intrinsic activity , phenylephrine , chemistry , melatonin , receptor antagonist , stimulation , agonist , antagonist , biology , blood pressure
Both α1‐ and β‐adrenergic receptors are present on ovine pineals. In the rat these two receptors interact so that activation of the α1‐receptor potentiates the β‐receptor‐mediated changes in cyclic AMP and the correlated changes in pineal N‐acetyltrans‐ferase (EC 2.3.1.87). Here we investigate possible interactions between α1‐ and β‐receptors through changes in cyclic AMP and assess the importance of each receptor to the melatonin response in ovine pineal punches/slices in vitro. The adrenergic agonists isoproterenol (ISO), noradrenaline (NA), and phenylephrine (PHE) stimulated dose‐dependent changes in cyclic AMP with the order of potency of ISO>NA>PHE, consistent with their relative binding affinities for the β‐receptor. The β‐receptor antagonist, propranolol, showed dose‐dependent inhibition of the ISO effect, whereas the α1‐selective antagonist, prazosin, had no effect. The S‐shape of the stimulation and inhibition curves for ISO reflects cyclic AMP changes mediated by the β‐receptor only without interaction through the α1‐receptor. Each of the adrenergic agonists stimulated indistinguishable dose‐dependent increases in melatonin release. The ability of PHE to stimulate changes in melatonin release in the absence of concomitant changes in cyclic AMP indicates an important role for the α1‐receptor. Prazosin inhibits this response, substantiating this conclusion. However, as propranolol is also inhibitory, it seems that the a 1‐receptor response is absolutely dependent upon a small level of β‐receptor stimulation, thus providing evidence for adrenergic receptor interaction at a step other than cyclic AMP.