L-DOPA Facilitates the Release of Endogenous Norepinephrine and Dopamine via Presynaptic β- and β-Adrenoceptors under Essentially Complete Inhibition of L-Aromatic Amino Acid Decarboxylase in Rat Hypothalamic Slices
Open Access
- 1 January 1990
- journal article
- research article
- Published by Elsevier in The Japanese Journal of Pharmacology
- Vol. 53 (1), 47-56
- https://doi.org/10.1254/jjp.53.47
Abstract
In rat hypothalamic slices, L-aromatic amino acid decarboxylae (AADC) was assayed, and the actions of L-DOPA on impulse (2 Hz)-evoked norepinephrine (NE) and dopamine (DA) release were studied under inhibition of aADC. Slices were incubated with L-DOPA, and DA and NE produced by conversion of the precursor were analyzed by high performance liquid chromatography with electrochemical detection (HPLC-ECD). In the slices, the Km and Vmax of AADC were 131 .mu.M and 122 pmol min/mg protein, respectively. NSD-1015, an AADC inhibitor, caused a noncompetitive type of inhibition, and the K1 value was 0.088 .mu.M. In the presence of 20 .mu.M NSD-1015, which was expected to cause 99.6% inhibition of AADC, L-DOPA (0.01-100 nM) concentration-dependently facilitated the release of NE from the superfused slices, and the L-DOPA (10 nM)-induced facilitation was antagonized by 100 nM ICI 89,406 and 100 nM ICI 118,551, a selecteive .beta.1- and .beta.2-adrenoceptor antagonist, respectively. This actin of L-DOPA was not modified by 30 .mu.M tropolone, an inhibitor of catechol-O-methyltransferase. L-DOPA at 0.01-1 nM similarly facilitated the release of DA. A quantitative analysis revealed that the L-DOPA-induced increase in NE and DA quantitative analysis revealed that the L-DOPA-induced increase in NE and DA release was much higher by a factor of 3 to 4 orders than was the amount of DA and NE converted from L-DOPA. These results add further support to the hypothesis that L-DOPA itself acts as a neuroactive substance in the rat central nervous system.Keywords
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