Cardiovascular actions of kinins in the rabbit

Publisher Website
Google Scholar
Abstract
The hypotensive action of bradykinin (BK) and congeners was measured in anesthetized rabbits by administering the peptides i.v. and intraarterially to evaluate their pulmonary inactivation. A systematic study of the distribution of receptors for BK in the cardiovascular system of the rabbit was approached: by measuring the myotropic effects of several peptides related to BK in strips of large arteries and veins; by recording the changes of tension and rate of isolated atria; by evaluating the changes of perfusion pressure in isolated hearts, kidneys and ears. This investigation was extended to strips of aortae of various mammals and to isolated atria of guinea pigs, for comparison. Receptors for BK were classified into 2 main types, B1 and B2, using the order of potency of 3 agonists [Tyr(Me)8]-BK, BK and [des-Arg9]-BK, and an antagonist, specific and competitive for the B1 receptors, the octapeptide [Leu-OMe8,des-Arg9]-BK. The complex cardiovascular effect of BK in vivo may result from direct actions on vascular smooth muscles, presumably mediated by at least 2 types of receptors, as well as from the release of endogenous prostaglandins. BK and congeners exert a direct action on vascular smooth muscle by stimulating specific receptors both of the B1 type (in the aorta, the large arteries and mesenteric vein) and of the B2 type (in the jugular vein); and these vascular tissues provide useful preparations for pharmacological studies of bradykinins. Isolated organs perfused through their main arteries with physiological medium respond to BK by an increase of perfusion pressure (vasoconstriction in isolated ears and kidneys) or by a decrease (vasodilation in the rabbit heart). The vascular effects of BK in the heart and the kidney depend in part on the release of endogenous prostaglandins and on the activation of receptors that appear to be of the B2 type. Like other endogenous hypotensive agents, BK appears to reduce the tonus of the peripheral vessels, while contracting large arteries and veins. The results obtained in vitro are discussed with respect to the hypotensive effect in vivo and to the role of kinins in inflammation and edema.