The importance of glutamate, glycine, and γ-aminobutyric acid transport and regulation in manganese, mercury and lead neurotoxicity

被引:81
作者
Fitsanakis, VA
Aschner, M
机构
[1] Vanderbilt Univ, Sch Med, Dept Pediat, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Med Ctr, Kennedy Ctr, Nashville, TN 37232 USA
关键词
glutamate; glycine; gamma-aminobutyric acid;
D O I
10.1016/j.taap.2004.11.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Historically, amino acids were studied in the context of their importance in protein synthesis. In the 1950s, the focus of research shifted as amino acids were recognized as putative neurotransmitters. Today, many amino acids are considered important neurochemicals. Although many amino acids play a role in neurotransmission, glutamate (Glu), glycine (Gly), and gamma-aminobutyric acid (GABA) are among the more prevalent and better understood. Glu, the major excitatory neurotransmitter, and Gly and GABA, the major inhibitory neurotransmitters, in the central nervous system, are known to be tightly regulated. Prolonged exposure to environmental toxicants, such as manganese (Mn), mercury (Hg), or lead (Pb), however, can lead to dysregulation of these neurochemicals and subsequent neurotoxicity. While the ability of these metals to disrupt the regulation of Glu, Gly and GABA have been Studied, few articles have examined the collective role of these amino acids in the respective metal's mechanism of toxicity. For each of the neurotransmitters above, we will provide a brief synopsis of their regulatory function, including the importance of transport and re-uptake in maintaining their optimal function. Additionally, the review will address the hypothesis that aberrant homeostasis of any of these amino acids, or a combination of the three, plays a role in the neurotoxicity of Mn, Hg, or pb. (c) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:343 / 354
页数:12
相关论文
共 102 条
[1]   Glutamate: A potential mediator of inorganic mercury neurotoxicity [J].
Albrecht, J ;
Matyja, E .
METABOLIC BRAIN DISEASE, 1996, 11 (02) :175-184
[2]   Mercuric chloride, but not methylmercury, inhibits glutamine synthetase activity in primary cultures of cortical astrocytes [J].
Allen, JW ;
Mutkus, LA ;
Aschner, M .
BRAIN RESEARCH, 2001, 891 (1-2) :148-157
[3]   MERCURY MODULATION OF GABA-ACTIVATED CHLORIDE CHANNELS AND NONSPECIFIC CATION CHANNELS IN RAT DORSAL-ROOT GANGLION NEURONS [J].
ARAKAWA, O ;
NAKAHIRO, M ;
NARAHASHI, T .
BRAIN RESEARCH, 1991, 551 (1-2) :58-63
[4]  
Aschner M, 1996, NEUROTOXICOLOGY, V17, P663
[5]   Methylmercury alters glutamate transport in astrocytes [J].
Aschner, M ;
Yao, CP ;
Allen, JW ;
Tan, KH .
NEUROCHEMISTRY INTERNATIONAL, 2000, 37 (2-3) :199-206
[6]  
ASCHNER M, 1996, NEUROTOXICOLOGY, V17, P277
[7]   ONTOGENY OF CATECHOLAMINE AND GABA LEVELS IN RAT-BRAIN - LACK OF EFFECT OF PERINATAL LEAD-EXPOSURE [J].
BAILEY, CC ;
KITCHEN, I .
TOXICOLOGY LETTERS, 1986, 30 (01) :97-102
[8]  
Bonilla E, 1994, Invest Clin, V35, P175
[9]   Lead increases tetrodotoxin-insensitive spontaneous release of glutamate and GABA from hippocampal neurons [J].
Braga, MFM ;
Pereira, EFR ;
Marchioro, M ;
Albuquerque, EX .
BRAIN RESEARCH, 1999, 826 (01) :10-21
[10]   Nanomolar concentrations of lead inhibit glutamatergic and GABAergic transmission in hippocampal neurons [J].
Braga, MFM ;
Pereira, EFR ;
Albuquerque, EX .
BRAIN RESEARCH, 1999, 826 (01) :22-34