Since Szentivanyi proposed the idea that asthma and other atopic ditseases are due to a P adrenergic defect there has been much interest in the role of the adrenergic receptors in allergy. The radioactive ligand binding techniques developed within the last few years have greatly increased our knowledge concerning the molecular nature of the adrenoceptors and the events following receptor sdmulation. The adrenoceptors have shown to be very dynamic structures. Their number and affinity may be altered due to various physiological and pharmacological stimuli. Their role in the pathogenesis of atopic diseases has not been definitely settled, but there seem to be a true beta adrenergic hyporesponsiveness and alpha hyperresponsiveness in asthma. This article briefly describes the radioligand binding technique and summarizes our present knowledge of the nature of the alpha and beta adrenoceptors and their possible role in atopic diseases.Key words: adrenergic receptors; atopy; asthma.
Accepted fcyr publication 11 January 1981, , , rr 1 , ^^ 01 receptor is defmed as a receptor for Functional subclassification of the adrenoceptorswhich epmephrme is a more potent stimulator It has been known since the beginning of the (agonist) than norepinephrine which again is century that the sympathomimetic amines have more potent than isoproterenol. The potency both excitatory and inhibitory effects in the of the amines was examined in intact animals organism. Early investigators proposed the or isolated organ preparations. In contrast, the existence of two fundamental types of mediator P receptor is defined as a receptor for which substances: an excitatory sympathin E and an isoproterenol is a more potent agonist than inhibitory sympathin I (1). As no amine which epinephrine which again is more potent than fulfilled the requirements for either sympathin norepinephrine. The development of relatively E or I could be found, the idea of two different selective a and |3 antagonists has further conreceptor types emerged. On the basis of the firmed the pharmacological usefulness of the a relative potency of six adrenergic amines on and P receptor concept. Table 1 summarizes various biological (mainly haemodynamic) pa-the major pharmacological characteristics of rameters, Ahlquist (1) defined two different the a and the j3 receptor. receptors: an a receptor which mediates most In 1967, Lands (55) showed that there is of the adrenergic amines' excitatory functions marked similarity between the relative poten-(vasoconstriction, pupil dilation, uterine con-cies of sympathomimetic amines on lipolysis traction) and a few inhibitory (intestinal relax-and cardiac stimulation on the one hand and ation), and a P receptor which mediates most of on bronchodilation and vasodepression on the the inhibitory functions (vasodilation, broncho-other. Furthermore, a potent lipolytic and cardilation, uterine relaxation) and a few excita-diac stimulating amine is a poor bronchodilator tory (cardiac inotropy and chronotropy).and vasodepressor. Therefore, Lands s...