AMINO-ACIDS DIFFERENTIALLY INHIBIT THE L-[H-3]ARGININE TRANSPORT AND NITRIC-OXIDE SYNTHASE IN RAT-BRAIN SYNAPTOSOMES

被引:20
作者
LOPES, MC
CARDOSO, SA
SCHOUSBOE, A
CARVALHO, AP
机构
[1] ROYAL DANISH SCH PHARM,PHARMABIOTEC RES CTR,DEPT BIOL SCI,COPENHAGEN,DENMARK
[2] UNIV COIMBRA,CTR NEUROSCI,DEPT ZOOL,COIMBRA,PORTUGAL
关键词
NITRIC OXIDE SYNTHASE INHIBITOR; RAT CORTEX SYNAPTOSOME; L-ARGININE TRANSPORT;
D O I
10.1016/0304-3940(94)90546-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The nitric oxide synthase (NOS) present in the cytosol obtained from rat cerebral cortex synaptosomes was inhibited by NG-nitro-L-arginine (L-NOArg) with an IC50 value of similar to 0.06 mu M. This compound did not affect the transport of L-arginine (L-Arg) into synaptosomes at concentrations up to 100 mu M but other potential inhibitors of NOS (N-G-monomethyl-L-arginine, N-G-amino-L-arginine and L-arginine methyl ester) inhibited L-Arg transport at a concentration <5 mu M. We showed that concentrations of L-NOArg (0.001-3 mu M) that did not block the uptake of tritiated arginine (L-[H-3]Arg) inhibited the catalytic activity of NOS in intact synaptosomes. L-NOArg at a concentration of 1 mu M inhibited the cytosolic enzyme by 98.0 +/- 2.0% of the total NOS activity whereas the enzyme studied in the intact synaptosomes was only inhibited by 75 +/- 5% which suggested that the NOS in synaptosomes is not fully accessible to the external L-NOArg. On the other hand, L-Lysine did not inhibit the cytosolic NOS activity of ruptured synaptosomes but at a concentration that blocked 50.0 +/- 4.5% of L-[H-3]Arg uptake it inhibited the NOS activity in intact synaptosomes by 12.6 +/- 3.6%, suggesting that the transport of L-Arg may be an important regulatory step in the pathway for nitric oxide generation.
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页码:1 / 4
页数:4
相关论文
共 15 条
[1]  
BANSINATH M, 1992, NEUROCHEM RES, V18, P1063
[2]   SELECTIVE TARGETING OF NITRIC-OXIDE SYNTHASE INHIBITORS TO SYSTEM Y(+) IN ACTIVATED MACROPHAGES [J].
BAYDOUN, AR ;
MANN, GE .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 200 (02) :726-731
[3]   IDENTIFICATION OF INHIBITORS OF NITRIC-OXIDE SYNTHASE THAT DO NOT INTERACT WITH THE ENDOTHELIAL-CELL L-ARGININE TRANSPORTER [J].
BOGLE, RG ;
MONCADA, S ;
PEARSON, JD ;
MANN, GE .
BRITISH JOURNAL OF PHARMACOLOGY, 1992, 105 (04) :768-770
[4]   NITRIC-OXIDE, A NOVEL NEURONAL MESSENGER [J].
BREDT, DS ;
SNYDER, SH .
NEURON, 1992, 8 (01) :3-11
[5]   NITRIC-OXIDE SYNTHASE FROM CEREBELLUM CATALYZES THE FORMATION OF EQUIMOLAR QUANTITIES OF NITRIC-OXIDE AND CITRULLINE FROM L-ARGININE [J].
BUSH, PA ;
GONZALEZ, NE ;
GRISCAVAGE, JM ;
IGNARRO, LJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 185 (03) :960-966
[6]  
CARVALHO AP, 1991, ANN NY ACAD SCI, V639, P301
[7]   GABA-MEDIATED CONTROL OF GLUTAMATE-DECARBOXYLASE (GAD) IN CELL AGGREGATE CULTURE OF CHICK-EMBRYO RETINA [J].
DEMELLO, FG .
DEVELOPMENTAL BRAIN RESEARCH, 1984, 14 (01) :7-13
[8]   RELATION OF EXOCYTOTIC RELEASE OF GAMMA-AMINOBUTYRIC-ACID TO CA-2+ ENTRY THROUGH CA-2+ CHANNELS OR BY REVERSAL OF THE NA(+)/CA-2+ EXCHANGER IN SYNAPTOSOMES [J].
DUARTE, CB ;
FERREIRA, IL ;
CARVALHO, AP ;
CARVALHO, CM .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1993, 423 (3-4) :314-323
[9]   REGIONAL DISTRIBUTION OF EDRF NO-SYNTHESIZING ENZYME(S) IN RAT-BRAIN [J].
FORSTERMANN, U ;
GORSKY, LD ;
POLLOCK, JS ;
SCHMIDT, HHHW ;
HELLER, M ;
MURAD, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 168 (02) :727-732
[10]   AMINO-ACID-TRANSPORT SYSTEMS IN THE HUMAN HEPATOMA-CELL LINE HEP-G2 [J].
GOENNER, S ;
BOUTRON, A ;
SONI, T ;
LEMONNIER, A ;
MOATTI, N .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 189 (01) :472-479