Age-related changes in nigrostriatal dopaminergic function are accentuated in ± brain-derived neurotrophic factor mice

被引:16
作者
Dluzen, DE
McDermott, JL
Anderson, LI
Kucera, J
Joyce, JN
Osredkar, T
Walro, JM
机构
[1] NE Ohio Univ, Coll Med, Dept Anat, Rootstown, OH 44272 USA
[2] Vet Adm Med Ctr Jamaica Plain, Boston, MA 02130 USA
[3] Sun Hlth Res Inst, Thomas H Christopher Ctr Parkinsons Dis Res, Sun City, AZ 85351 USA
关键词
dopamine; age; striatum; sensorimotor; locomotor; Parkinson's disease;
D O I
10.1016/j.neuroscience.2004.06.032
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of a deletion for the brain derived neurotrophic factor (BDNF) allele ( +/- BDNF) upon age-related changes in nigrostriatal dopaminergic (NSDA) function were assessed. Behavioral (beam crossing and spontaneous activity) and neurochemical (potassium-stimulated dopamine release from superfused striatum) measures were compared among Young (4-5 month), Middle (11-13 month) and Aged (19-21 month) +/- BDNF and their wild type littermate control (+/+ BDNF) mice. No statistically significant differences were obtained between +/+ and +/- BDNF mice at the Young age sampling period for any of the behavioral or neurochemical measures. Behavioral and neurochemical responses indices of NSDA function begin to diverge between +/+ and +/- Middle age BDNF mice and maximal differences were observed at the Aged period. For both movement and stereotypy times, scores obtained from +/+ mice were significantly decreased compared with +/- BDNF mice at the Aged period and center time scores of +/+ mice were decreased at both the Middle and Aged periods compared with BDNF mice. Neurochemically, potassium-stimulated DA release of +/+ mice was significantly greater than +/- BDNF mice with maximal differences obtained at the Aged period. These results demonstrate marked differences in age-related changes of NSDA function between +/+ and +/- BDNF mice and suggest that the deletion of one allele for BDNF may make these mice more susceptible to age-related declines in NSDA function. (C) 2004 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:201 / 208
页数:8
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