Abstract
1. Recovery of 3H-dopamine and 3H-L-dopa infused intra-arterially at a constant rate of 20 ng/min into the cat spleen perfused with Krebs bicarbonate solution was 52·6±3·8% and 90·5±3·1% respectively. Recovery of 3H-dopamine in spleens treated with α-methyl-p-tyrosine was 67·7±6·7% and was not significantly different from untreated spleens.
2. Release of 3H-dopamine by nerve stimulation after an infusion of 3H-dopamine resembled release of endogenous noradrenaline. Release of 3H-L-dopa and 3H-L-tyrosine after their infusion did not occur in any consistent manner by nerve stimulation.
3. Preferential release of 3H-noradrenaline formed from 3H-dopamine was not observed during continuous nerve stimulation. Specific activity of released 3H-noradrenaline remained constant during any single stimulation period with or without 3H-dopamine infusion. Treating the cats with α-methyl-p-tyrosine did not change the time course of 3H-noradrenaline release.
4. Output of noradrenaline expressed as a percentage of the first minute output in both normal and α-methyl-p-tyrosine treated spleens was not significantly different at various times during continuous nerve stimulation.
5. Specific activity of released noradrenaline formed from 3H-dopamine was always greater than the specific activity of the spleen in normal spleens and spleens treated with α-methyl-p-tyrosine.
6. It is concluded that newly synthesized or infused noradrenaline initially mixes with a more rapidly turning pool and only slowly with the entire tissue store. During continuous nerve stimulation there is no further preferential release of newly synthesized noradrenaline. Released noradrenaline truly represents the state of the releasable pool and will vary with the latter.
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