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      Metabolism of Exogenous Noradrenaline in Constricted and in Distended Rabbit Ear Arteries

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      Journal of Vascular Research

      S. Karger AG

      Noradrenaline, Metabolism, Distension, Constriction, Perfused artery

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          (1) The metabolism of extraluminal and of intraluminal <sup>3</sup>H-noradrenaline (<sup>3</sup>H-NA; 0.18 µmol/l) was examined in arteries from reserpine-pretreated rabbits. The arteries were perfused in Ca medium (a) in the absence of prazosin to permit constriction to occur, (b) in the presence of prazosin, and (c) at a high intraluminal pressure (110 mm Hg; prazosin present) in order to distend the vessel. (2) The constrictor activity of the extraluminal NA was extremely weak, and antagonism by prazosin was not associated with a change in metabolite formation. The only change accompanying distension was a small (24%) increase in 3,4-dihydroxyphenylethylene glycol (DOPEG) formation.(3) The constrictor activity of intraluminal NA was much stronger than that of extraluminal NA. Antagonism of constriction by prazosin was accompanied by a 5-fold increase in DOPEG formation and a 2-fold increase in normetanephrine (NMN) formation. Distension resulted in a further 3-fold increase in DOPEG formation, but had little effect on NMN formation.(4) Since DOPEG is neuronal in origin, it is suggested that the changes in DOPEG formation in point 3 above reflect changes in the rate at which the intraluminal NA diffuses into the region of the sympathetic nerve terminals. In support of this suggestion, (a) distension was without effect when DOPEG formation was related to the vascular dimensions which determine rate of diffusion of NA, instead of to vascular mass, and (b) effects of constriction and distension on the rate of diffusion of intraluminal <sup>14</sup>C-sorbitol across the artery wall paralleled their effects on DOPEG formation.

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          Author and article information

          J Vasc Res
          Journal of Vascular Research
          S. Karger AG
          23 September 2008
          : 25
          : 4
          : 185-198
          Department of Clinical and Experimental Pharmacology, University of Adelaide, S.A., Australia
          158731 Blood Vessels 1988;25:185–198
          © 1988 S. Karger AG, Basel

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          Page count
          Pages: 14
          Research Paper


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