L-DOPA FACILITATES THE RELEASE OF ENDOGENOUS NOREPINEPHRINE AND DOPAMINE VIA PRESYNAPTIC BETA-1-ADRENOCEPTORS AND BETA-2-ADRENOCEPTORS UNDER ESSENTIALLY COMPLETE INHIBITION OF L-AROMATIC AMINO-ACID DECARBOXYLASE IN RAT HYPOTHALAMIC SLICES

被引:42
|
作者
GOSHIMA, Y
NAKAMURA, S
MISU, Y
机构
[1] Department of Pharmacology, Yokohama City University School of Medicine, Yokohama
来源
JAPANESE JOURNAL OF PHARMACOLOGY | 1990年 / 53卷 / 01期
关键词
D O I
10.1254/jjp.53.47
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In rat hypothalamic slices, L-aromatic amino acid decarboxylase (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 μM and 122 pmol/min/mg protein, respectivelv. NSD-1015, an AADC inhibitor, caused a noncompetitive type of inhibition, and the Ki value was 0.086 μM. In the presence of 20 μM NSD-101 5, 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 selective μ1 and μ2-adrenoceptor antagonist, respectively. This action of L-DOPA was not modified by 30/M tropolone, an inhibitor of catechol-O-methyl-transferase. 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 release was much higher by a factor of 3 to 4 ordres 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. © 1990, The Japanese Pharmacological Society. All rights reserved.
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页码:47 / 56
页数:10
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