Deficiencies of hippocampal Zn and ZnT3 accelerate brain aging of rat

被引:50
作者
Saito, T [1 ]
Takahashi, K
Nakagawa, N
Hosokawa, T
Kurasaki, M
Yamanoshita, O
Yamamoto, Y
Sasaki, H
Nagashima, K
Fujita, H
机构
[1] Hokkaido Univ, Sch Med, Div Neurol Sci, Lab Environm Biol, Sapporo, Hokkaido 0608638, Japan
[2] Hokkaido Univ, Sch Med, Div Neurol Sci, Lab Mol & Cellular Pathol, Sapporo, Hokkaido 0608638, Japan
[3] Hokkaido Univ, Ctr Res & Dev Higher Educ, Sapporo, Hokkaido 0600817, Japan
[4] Hokkaido Univ, Grad Sch Environm Earth Sci, Dept Environm Med & Informat, Sapporo, Hokkaido 0600810, Japan
关键词
Zn; aging; learning and memory; senescence acceleration; SAM; brain; glutamate; neuronal cell death; Zn transporters;
D O I
10.1006/bbrc.2000.3946
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
We examined the link of hippocampal Zn to the functional impairments with aging using senescence-accelerated mouse prone 10 (SAMP10) with deficits in learning and memory. Zn in hippocampal mossy fiber pathway was less distributed in aged SAMP10 than that in the age-matched control. Furthermore, expression of Zn transporter 3, ZnT3, which plays to accumulate Zn in synaptic vesicles in the mossy fiber pathway, was markedly reduced in the hippocampal region even in young SAMP10. Moreover, excessive presynaptic release of glutamate as well as glycine and expression of glial fibrillary acidic protein, a marker of neuronal cell injury, were observed in the hippocampus of aged SAMP10 compared to the control. The present results suggest that age-dependent deficiencies of Zn in synaptic vesicles of the mossy fiber pathway induced by low expression of ZnT3 cause glutamatergic excitotoxicity in the hippocampal neurons and the deterioration of learning and memory in SAMP10. (C) 2000 Academic Press.
引用
收藏
页码:505 / 511
页数:7
相关论文
共 38 条
[1]   RELEASE OF ENDOGENOUS ZN-2+ FROM BRAIN-TISSUE DURING ACTIVITY [J].
ASSAF, SY ;
CHUNG, SH .
NATURE, 1984, 308 (5961) :734-736
[2]   Age-related changes of sulphide-silver staining in the rat hippocampus [J].
Barili, P ;
Fringuelli, C ;
Ricci, A ;
Rossodivita, I ;
Sabbatini, M .
MECHANISMS OF AGEING AND DEVELOPMENT, 1997, 99 (02) :83-94
[3]   NORMAL AGING - REGIONALLY SPECIFIC CHANGES IN HIPPOCAMPAL SYNAPTIC TRANSMISSION [J].
BARNES, CA .
TRENDS IN NEUROSCIENCES, 1994, 17 (01) :13-18
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   LEAD AND ZINC BLOCK A VOLTAGE-ACTIVATED CALCIUM-CHANNEL OF APLYSIA NEURONS [J].
BUSSELBERG, D ;
EVANS, ML ;
RAHMANN, H ;
CARPENTER, DO .
JOURNAL OF NEUROPHYSIOLOGY, 1991, 65 (04) :786-795
[6]  
CHARTON G, 1985, EXP BRAIN RES, V58, P202
[7]   GLUTAMATE NEUROTOXICITY AND DISEASES OF THE NERVOUS-SYSTEM [J].
CHOI, DW .
NEURON, 1988, 1 (08) :623-634
[8]   Zinc and brain injury [J].
Choi, DW ;
Koh, JY .
ANNUAL REVIEW OF NEUROSCIENCE, 1998, 21 :347-375
[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]   Zinc metabolism in the brain: Relevance to human neurodegenerative disorders [J].
Cuajungco, MP ;
Lees, GJ .
NEUROBIOLOGY OF DISEASE, 1997, 4 (3-4) :137-169