RT Journal Article
SR Electronic
T1 EFFECT OF THE CHELATING AGENTS, EDTA, 2,2'-BIPYRIDINE, 8-HYDROXYQUINOLINE AND PYROPHOSPHORIC ACID, ON NOREPINEPHRINE UPTAKE BY RABBIT AORTA
JF Journal of Pharmacology and Experimental Therapeutics
JO J Pharmacol Exp Ther
FD American Society for Pharmacology and Experimental Therapeutics
SP 136
OP 146
VO 163
IS 1
A1 OVE A. NEDERGAARD
A1 AUGUSTIN VAGNE
A1 JOHN A. BEVAN
YR 1968
UL http://jpet.aspetjournals.org/content/163/1/136.abstract
AB The uptake of tritiated norepinephrine by rabbit isolated aortic rings after 1 hr was enhanced by the chelating agents, (ethylenedinitrilo) tetraacetic acid (EDTA), either as the disodium salt (Na2EDTA) or as the calcium disodium salt (CaNa2EDTA), and sodium pyrophosphate, but not by 2,2'-bipyridine and 8-hydroxyquinoline. The enhanced norepinephrine uptake seen with CaNa2EDTA was inhibited by 8-hythoxyquinoline but not by 2,2'-bipyridine. In the absence of CaNa2EDTA, repeated replacement of the bath fluid with physiologic salt solution to which tritiated norepinephrine had been added immediately before increased the uptake to a level close to that seen in the presence of CaNa2EDTA. The removal of Ca++ and Mg++ either singly or together, from the physiologic salt solution had no effect on the EDTA-enhanced norepinephrine uptake. However, in the absence of both cations this uptake was decreased when Na3EDTA was present in a concentration much higher than that necessary for causing maximal enhancement of norepinephrine uptake. The neurogenic contractile response of the rabbit isolated nerve-pulmonary artery preparation was blocked by Na2EDTA, 2,2'-bipyridine and 8-hydroxyquinoline, but not by CaNa2EDTA. Ca++ reversed only the Na2EDTA-induced block. The contractile response of the artery to exogenous norepinephrine and serotonin was not altered by Na2EDTA, but was inhibited by 2,2'-bipyridine and 8-hydroxyquinoline. These results support the view that EDTA acts by preventing the oxidation of norepinephrine catalyzed by traces of heavy metals in the physiologic salt solution. It is concluded that it is essential to use EDTA to stabilize norepinephrine when the uptake of this amine is studied. Furthermore, EDTA in concentrations sufficient to cause maximum enhancement of uptake does not interfere with adrenergic neuroeffector transmission. The inhibition of this process and of norepinephrine uptake seen with 2 ,2'-bipyridine and 8-hydroxyquinoline may be due to toxic metal chelates formed by these agents with the trace metals. © 1968, by The Williams & Wilkins Company