Enriched environment elevates expression of growth associated protein-43 in the substantia nigra of SAMP8 mice

被引:1
|
作者
Zhen-Yun Yuan [1 ,2 ]
Jie Yang [1 ,2 ]
Xiao-Wei Ma [1 ,2 ]
Yan-Yong Wang [1 ,2 ]
Ming-Wei Wang [1 ,2 ]
机构
[1] The First Hospital of Hebei Medical University
[2] Brain Aging and Cognitive Neuroscience Laboratory of Hebei Province
关键词
nerve regeneration; Parkinson’s disease; neural plasticity; senescence-accelerated mouse prone 8; growth associated protein-43; substantia nigra; learning and memory; neural regeneration;
D O I
暂无
中图分类号
R741 [神经病学];
学科分类号
1002 ;
摘要
An enriched environment protects dopaminergic neurons from 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine(MPTP)-induced neuronal injury, but the underlying mechanism for this is not clear. Growth associated protein-43(GAP-43) is closely associated with neurite outgrowth and axon regeneration during neural development. We speculate that an enriched environment can reduce damage to dopaminergic neurons by affecting the expression of GAP-43. This study is designed to test this hypothesis. Three-month-old female senescence-accelerated mouse prone 8(SAMP8) mice were housed for 3 months in an enriched environment or a standard environment. These mice were then subcutaneously injected in the abdomen with 14 mg/kg MPTP four times at 2-hour intervals. Morris water maze testing demonstrated that learning and memory abilities were better in the enriched environment group than in the standard environment group. Reverse-transcription polymerase chain reaction, immunohistochemistry and western blot assays showed that m RNA and protein levels of GAP-43 in the substantia nigra were higher after MPTP application in the enriched environment group compared with the standard environment group. These findings indicate that an enriched environment can increase GAP-43 expression in SAMP8 mice. The upregulation of GAP-43 may be a mechanism by which an enriched environment protects against MPTP-induced neuronal damage.
引用
收藏
页码:1988 / 1994
页数:7
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