RT Journal Article
SR Electronic
T1 Inactivation of neural and exogenous norepinephrine in rat tail artery studied by the oil immersion technique.
JF Journal of Pharmacology and Experimental Therapeutics
JO J Pharmacol Exp Ther
FD American Society for Pharmacology and Experimental Therapeutics
SP 102
OP 111
VO 198
IS 1
A1 Wyse, D G
YR 1976
UL http://jpet.aspetjournals.org/content/198/1/102.abstract
AB The inactivation of exogenous and neural norepinephrine (NE) by helical strips of rat tail artery was studied with a combination of the techniques of transmural stimulation and oil immersion. A steady-state contraction was elicited either by adding low concentrations of NE to the bath or by low frequency transmural stimulation. The aqueous bath solution was then replaced with mineral oil and relaxation was monitored. A prolongation of the rate of relaxation of the strip at a given concentration of exogenous NE or frequency of transmural stimulation indicates that inactivation of NE has been slowed. The major known processes for inactivation of NE were inhibited by pharmacological agents used singly or in various combinations (uptake by cocaine, uptake by corticosterone, catechol-O-methyltransferase by tropolone and monoamine oxidase by iproniazid). Cocaine was the only agent which alone caused a marked shift in the relaxation curve. A modest and equivocal effect on relaxation after inhibition of extraneuronal uptake (uptake), or catabolism of NE (catechol-O-methyltransferase and monoamine oxidase) was only demonstrated under special circumstances (high concentrations of NE, combinations of inhibitors, or uptake simultaneously inhibited). The data suggest that low concentrations of NE, both exogenous and neural, are preferentially inactivated in rat tail artery by neuronal uptake and storage.