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The effects of atriopeptin II on calcium fluxes in rabbit aorta
Authors:P J Chiu  G Tetzloff  E J Sybertz
Affiliation:1. Emory University School of Medicine, Department of Emergency Medicine, 550 W Peachtree St NW, Atlanta, GA 30308, United States of America.;2. Emory University, Emergency Medicine Clinical Pharmacy Specialist, Department of Pharmacy, 550 W Peachtree St NW, Atlanta, GA 30308, United States of America.;3. University of Georgia College of Pharmacy, 550 W Peachtree St NW, Atlanta, GA 30308, United States of America.;2. Diabetes and Obesity Center, University of Louisville, Louisville, KY, United States;1. Laboratory of Electrochemical Engineering (LEE), Department of Chemical Engineering, University of the Philippines Diliman, Quezon City 1101, Philippines;2. Energy Engineering Program, National Graduate School of Engineering (NGSE), College of Engineering, University of the Philippines Diliman, Quezon City 1101, Philippines
Abstract:Effects of atriopeptin II (AP II) at 10(-7) M on the 45Ca flux and contractile responses to vasoconstrictors including norepinephrine (NE), angiotensin II (angio II) and high K were studied in isolated rabbit aortic strips. Augmentation of 45Ca efflux from aorta in normal physiological saline (PSS) due to NE and angio II each at 3 X 10(-7) M was greatly inhibited by AP II, suggesting that stimulated increase in cytosolic Ca2+ was suppressed. In contrast, the 45Ca efflux responses to KCl (20 and 40 mM) were not affected by AP II. Furthermore, the marked inhibition of contractile responses to NE (-58%) and angio II (-57%) by AP II was accompanied by significant decreases in 45Ca influx, whereas AP II exhibited only a modest inhibition on KCl (40 mM)-induced contraction (-28%) without affecting the accompanying increase in 45Ca influx. The 45Ca efflux from aortae in Ca2+-free PSS due to NE was markedly diminished by AP II, suggesting impairment of intracellular Ca2+ release. With tissues in either a basal or post-stimulation state (tissue Ca2+ previously increased with KCl stimulation), AP II did not stimulate 45Ca efflux in Ca2+-free PSS, suggesting its lack of effect on Ca extrusion. It is concluded that AP II is preferentially antagonistic against vascular responses to NE and angio II vs. high K and that inhibition of Ca entry and release forms the primary basis of its potent vasorelaxant action against vasoconstrictors.
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