Zinc homeostasis and functions of zinc in the brain

被引:273
作者
Takeda, A [1 ]
机构
[1] Univ Shizuoka, Sch Pharmaceut Sci, Dept Radiobiochem, Shizuoka 4228526, Japan
关键词
brain function; limbic system; vesicular zinc; zinc deprivation; zinc homeostasis;
D O I
10.1023/A:1012982123386
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The brain barrier system, i.e., the blood-brain and blood-cerebrospinal fluid barriers, is important for zinc homeostasis in the brain. Zinc is supplied to the brain via both barriers. A large portion of zinc serves as zinc metalloproteins in neurons and glial cells. Approximately 10% of the total zinc in the brain, probably ionic zinc, exists in the synaptic vesicles, and may serve as an endogenous neuromodulator in synaptic neurotransmission. The turnover of zinc in the brain is much slower than in peripheral tissues such as the liver. However, dietary zinc deprivation affects zinc homeostasis in the brain. Vesicular zinc-enriched regions, e.g., the hippocampus, are responsive to dietary zinc deprivation, which causes brain dysfunctions such as learning impairment and olfactory dysfunction. Olfactory recognition is reversibly disturbed by the chelation of zinc released from amygdalar neuron terminals. On the other hand, the susceptibility to epileptic seizures, which may decrease vesicular zinc, is also enhanced by zinc deficiency. Therefore, zinc homeostasis in the brain is closely related to neuronal activity. Even in adult animals and probably adult humans, adequate zinc supply is important for brain functions and prevention of neurological diseases.
引用
收藏
页码:343 / 351
页数:9
相关论文
共 135 条
[1]   EFFECTS OF HISTIDINE ON TISSUE ZINC DISTRIBUTION IN RATS [J].
AIKEN, SP ;
HORN, NM ;
SAUNDERS, NR .
BIOMETALS, 1992, 5 (04) :235-243
[2]   Regulation of metallothionein-III (GIF) mRNA in the brain of patients with Alzheimer disease is not impaired [J].
Amoureux, MC ;
Van Gool, D ;
Herrero, MT ;
Dom, R ;
Colpaert, FC ;
Pauwels, PJ .
MOLECULAR AND CHEMICAL NEUROPATHOLOGY, 1997, 32 (1-3) :101-121
[3]   RELEASE OF ENDOGENOUS ZN-2+ FROM BRAIN-TISSUE DURING ACTIVITY [J].
ASSAF, SY ;
CHUNG, SH .
NATURE, 1984, 308 (5961) :734-736
[4]  
BUXANIRICE S, 1994, J NEUROCHEM, V62, P665
[5]   ZINC NEUROTOXICITY IN CORTICAL CELL-CULTURE [J].
CHOI, DW ;
YOKOYAMA, M ;
KOH, J .
NEUROSCIENCE, 1988, 24 (01) :67-79
[6]   Zinc and brain injury [J].
Choi, DW ;
Koh, JY .
ANNUAL REVIEW OF NEUROSCIENCE, 1998, 21 :347-375
[7]  
Christensen MK, 1998, J COMP NEUROL, V400, P375, DOI 10.1002/(SICI)1096-9861(19981026)400:3<375::AID-CNE7>3.0.CO
[8]  
2-5
[9]   Elimination of zinc from synaptic vesicles in the intact mouse brain by disruption of the ZnT3 gene [J].
Cole, TB ;
Wenzel, HJ ;
Kafer, KE ;
Schwartzkroin, PA ;
Palmiter, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (04) :1716-1721
[10]   Seizures and neuronal damage in mice lacking vesicular zinc [J].
Cole, TB ;
Robbins, CA ;
Wenzel, HJ ;
Schwartzkroin, PA ;
Palmiter, RD .
EPILEPSY RESEARCH, 2000, 39 (02) :153-169