期刊
NEUROSCIENCE LETTERS
卷 468, 期 2, 页码 151-155出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2009.10.087
关键词
Amyloid-beta; Hippocampus; Neurodegeneration; Spatial memory
资金
- CONACYT [61205]
- INNN [15/06]
- UNAM PAPIIT [IN214609, IN212108]
- Laboratory of Neuropharmacology-BUAP [LNAB1-08]
Alzheimer's disease (AD) is characterized by the amyloid-beta (A beta) aggregation but it is unclear when this process begins. Previously, we showed that amyloid-beta(25-35) (A beta((25-35))) increases the nitric oxide (NO) pathways and causes neurodegenerative effects in rats. The excessive increase of NO during brain development can promote a persistent oxidative stress, but the role of the A beta((25-35)) in the neonatal age and its effects over the long term is unclear. Our aim was to evaluate if the A beta((25-35)) injection on postnatal day 7 causes loss in spatial memory by NO pathways in adult rats. Our results showed that neonatal-A beta((25-35)) injection into the hippocampus (Hp) causes significant impairments in the spatial memory after 90 days. The NO levels were found increased and argynophilic in the Hp. Other evidence of neuronal damage was an increase of the immunoreactivity for 3-nitrotyrosine (3-NT) and the glial-fibrilar acid protein (GFAP) in the Hp of the A beta((25-35)) group. In contrast, these effects were blocked by the administration of L-NAME (inhibitor of nitric oxide synthase) before the injection of A beta((25-35)). The L-NAME plus A beta((25-35)) group showed a better performance in the spatial memory compared to the A beta((25-35)) group. In addition in this group we found a decrease of NO, 3-NT and neurodegeneration in the Hp compared to the A beta((25-35)) group. This finding is a novel result about the role of A beta((25-35)) during the neonatal stage that enhances the NO production, which appears to impair the spatial memory in adult rats. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据