Effects of methylmalonic and propionic acids on glutamate uptake by synaptosomes and synaptic vesicles and on glutamate release by synaptosomes from cerebral cortex of rats

被引:22
作者
Brusque, AM [1 ]
Rotta, LN [1 ]
Tavares, RG [1 ]
Emanuelli, T [1 ]
Schwarzbold, CV [1 ]
Dutra, CS [1 ]
Wyse, ATD [1 ]
Wannmacher, CMD [1 ]
de Souza, DOG [1 ]
Wajner, M [1 ]
机构
[1] Univ Fed Rio Grande do Sul, Inst Ciencias Basicas Saude, Dept Bioquim, BR-90035003 Porto Alegre, RS, Brazil
关键词
methylmalonic acid; propionic acid; methylmalonic acidemia; propionic acidemia; excitotoxicity; glutamate;
D O I
10.1016/S0006-8993(01)03069-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurological dysfunction is common in patients with methylmalonic and propionic acidemias. However, the mechanisms underlying the neuropathology of these disorders are far from understood. In the present study we investigated the in vitro effects of methylmalonic (MMA) and propionic (PA) acids at various concentrations (1 muM-5 mM) on three parameters of the glutamatergic system, namely the basal wind potassium-induced release of L-[H-3]glutamate by synaptosomes. Na+-dependent L-[H-3]glutamate uptake by synaptosomes and Na+-independent L-[H-3]glutamate uptake by synaptic vesicle, from cerebral cortex of male adult Wistar rat,. The results showed that MMA significantly increased potassium-induced but not basal L-[H-3]glutamate release from synaptosomes with no alteration in synaptosomal L-[H-3]glutamate uptake. A significant reduction of L-[H-3]glutamate incorporation into vesicles caused by MMA was also detected. In contrast, PA had no effect on these parameters. These findings indicate that MMA alters the glutamatergic system. Although additional studies are necessary to evaluate the importance of these observations for the neuropathology of methylmalonic acidemia, it is possible that the effects elicited by MMA may lead to excessive glutamate concentrations at the synaptic cleft, a fact that may explain previous in vivo and in vitro findings associating MMA with excitotoxicity. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:194 / 201
页数:8
相关论文
共 58 条
[1]   NONVESICULAR RELEASE OF NEUROTRANSMITTER [J].
ATTWELL, D ;
BARBOUR, B ;
SZATKOWSKI, M .
NEURON, 1993, 11 (03) :401-407
[2]   DOES IMPAIRMENT OF ENERGY-METABOLISM RESULT IN EXCITOTOXIC NEURONAL DEATH IN NEURODEGENERATIVE ILLNESSES [J].
BEAL, MF .
ANNALS OF NEUROLOGY, 1992, 31 (02) :119-130
[3]   ELEVATION OF THE EXTRACELLULAR CONCENTRATIONS OF GLUTAMATE AND ASPARTATE IN RAT HIPPOCAMPUS DURING TRANSIENT CEREBRAL-ISCHEMIA MONITORED BY INTRACEREBRAL MICRODIALYSIS [J].
BENVENISTE, H ;
DREJER, J ;
SCHOUSBOE, A ;
DIEMER, NH .
JOURNAL OF NEUROCHEMISTRY, 1984, 43 (05) :1369-1374
[4]   Magnetic resonance imaging and spectroscopy of the brain in propionic acidemia: Clinical and biochemical considerations [J].
Bergman, AJIW ;
VanderKnaap, MS ;
Smeitink, JAM ;
Duran, M ;
Dorland, L ;
Valk, J ;
PollThe, BT .
PEDIATRIC RESEARCH, 1996, 40 (03) :404-409
[5]   A presynaptic N-methyl-D-aspartate autoreceptor in rat hippocampus modulating amino acid release from a cytoplasmic pool [J].
Breukel, AIM ;
Besselsen, E ;
da Silva, FHL ;
Ghijsen, WEJM .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1998, 10 (01) :106-114
[6]  
BRISMAR J, 1994, AM J NEURORADIOL, V15, P1459
[7]  
Brusque AM, 1997, MED SCI RES, V25, P347
[8]   Chronic administration of propionic acid reduces ganglioside N-acetylneuraminic acid concentration in cerebellum of young rats [J].
Brusque, AM ;
Terracciano, ST ;
Fontella, FU ;
Vargas, C ;
da Silva, CG ;
Wyse, AT ;
Trindade, VMT ;
Wannmacher, CMD ;
Wajner, M .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1998, 158 (02) :121-124
[10]   Methylmalonic and propionic acids increase the in vitro incorporation of 32P into cytoskeletal proteins from cerebral cortex of young rats through NMDA glutamate receptors [J].
de Mattos-Dutra, A ;
Meirelles, R ;
da Rocha, BB ;
Kommers, T ;
Wofchuk, ST ;
Wajner, M ;
Pessoa-Pureur, R .
BRAIN RESEARCH, 2000, 856 (1-2) :111-118