Age-related changes in expression of hippocalcin and NVP2 in rat brain

被引:27
作者
Furuta, Y [1 ]
Kobayashi, M [1 ]
Masaki, T [1 ]
Takamatsu, K [1 ]
机构
[1] Toho Univ, Sch Med, Dept Physiol, Ohta Ku, Tokyo 1438540, Japan
关键词
aging; cerebral cortex; hippocalcin; hippocampus; neural visinin-like calcium-binding protein 2 (NVP2); rat;
D O I
10.1023/A:1021000425070
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
Expression of hippocalcin and neural visinin-like calcium-binding protein 2 (NVP2) in aging rat brain was investigated by immunoblot and immunohistochemical analyses. In 3-month old rats, hippocalcin and NVP2 were present at high concentrations in hippocampal and cerebral pyramidal cells and dentate granule cells, with hippocalcin protein levels being five to ten times higher than NVP2 levels. Hippocalcin levels in hippocampus and cerebral cortex decreased by approximately 20% at 24 months. While the number of hippocalcin-positive cells in CA3, dentate gyrus and cerebral cortex were preserved, staining intensity decreased. In contrast, the number and staining intensity of hippocalcin-positive cells in CA1 were maintained. NVP2 levels in hippocampus and cerebral cortex decreased by approximately 30% at 24 months. In cerebral cortex, the number and intensity of NVP2-positive cells decreased. In CA1 through CA3 and in dentate gyrus, NVP2-positive cell numbers were preserved, but staining intensity decreased. In summary, the loss of hippocalcin and NVP2 in aging rat brain may be associated with age-related impairment of postsynaptic functions.
引用
收藏
页码:651 / 658
页数:8
相关论文
共 51 条
[1]  
ADAMS I, 1987, CURRENT TOPICS RES S, V4
[2]   CALCIUM-BINDING PROTEINS IN THE NERVOUS-SYSTEM [J].
BAIMBRIDGE, KG ;
CELIO, MR ;
ROGERS, JH .
TRENDS IN NEUROSCIENCES, 1992, 15 (08) :303-308
[3]   REGION-SPECIFIC AGE EFFECTS ON AMPA SENSITIVITY - ELECTROPHYSIOLOGICAL EVIDENCE FOR LOSS OF SYNAPTIC CONTACTS IN HIPPOCAMPAL FIELD CA1 [J].
BARNES, CA ;
RAO, G ;
FOSTER, TC ;
MCNAUGHTON, BL .
HIPPOCAMPUS, 1992, 2 (04) :457-468
[4]   Functional integrity of NMDA-dependent LTP induction mechanisms across the lifespan of F-344 rats [J].
Barnes, CA ;
Rao, G ;
McNaughton, BL .
LEARNING & MEMORY, 1996, 3 (2-3) :124-137
[5]   Age-related decrease in the N-methyl-D-aspartate(R)-mediated excitatory postsynaptic potential in hippocampal region CA1 [J].
Barnes, CA ;
Rao, G ;
Shen, J .
NEUROBIOLOGY OF AGING, 1997, 18 (04) :445-452
[6]   PHYSIOLOGICAL COMPENSATION FOR LOSS OF AFFERENT SYNAPSES IN RAT HIPPOCAMPAL GRANULE CELLS DURING SENESCENCE [J].
BARNES, CA ;
MCNAUGHTON, BL .
JOURNAL OF PHYSIOLOGY-LONDON, 1980, 309 (DEC) :473-485
[7]   NORMAL AGING - REGIONALLY SPECIFIC CHANGES IN HIPPOCAMPAL SYNAPTIC TRANSMISSION [J].
BARNES, CA .
TRENDS IN NEUROSCIENCES, 1994, 17 (01) :13-18
[8]   NMDA DEPOLARIZATIONS AND LONG-TERM POTENTIATION ARE REDUCED IN THE AGED RAT NEOCORTEX [J].
BASKYS, A ;
REYNOLDS, JN ;
CARLEN, PL .
BRAIN RESEARCH, 1990, 530 (01) :142-146
[9]  
Braunewell KH, 1997, J NEUROCHEM, V68, P2129
[10]   SYNAPTIC LOSS IN COGNITIVELY IMPAIRED AGED RATS IS AMELIORATED BY CHRONIC HUMAN NERVE GROWTH-FACTOR INFUSION [J].
CHEN, KS ;
MASLIAH, E ;
MALLORY, M ;
GAGE, FH .
NEUROSCIENCE, 1995, 68 (01) :19-27