Age-related toxicity of amyloid-beta associated with increased pERK and pCREB in primary hippocampal neurons: reversal by blueberry extract

被引:46
作者
Brewer, Gregory J. [1 ,2 ,3 ]
Torricelli, John R. [1 ]
Lindsey, Amanda L. [1 ]
Kunz, Elizabeth Z. [1 ]
Neuman, A. [4 ]
Fisher, Derek R. [4 ]
Joseph, James A. [4 ]
机构
[1] So Illinois Univ, Sch Med, Dept Med Microbiol Immunol & Cell Biol, Springfield, IL 62794 USA
[2] So Illinois Univ, Sch Med, Dept Neurol, Springfield, IL 62794 USA
[3] So Illinois Univ, Sch Med, Dept Pharmacol, Springfield, IL 62794 USA
[4] Tufts Univ, USDA HNRC, Boston, MA 02111 USA
关键词
Aging; Neurotoxicity; Amyloid-beta; Stress signaling; Oxyradicals; Glutathione; PROTEIN-KINASE-C; OXIDATIVE STRESS; IMMUNOCYTOCHEMICAL LOCALIZATION; CALCIUM HOMEOSTASIS; BEHAVIORAL DEFICITS; SIGNAL-TRANSDUCTION; ALZHEIMERS-DISEASE; ADULT; CELLS; ACTIVATION;
D O I
10.1016/j.jnutbio.2009.08.005
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
Further clarification is needed to address the paradox that memory formation, aging and neurodegeneration all involve calcium influx, oxyradical production (ROS) and activation of certain signaling pathways. In aged rats and in APP/PS-1 mice, cognitive and hippocampal Ca2+ dysregulation was reversed by food supplementation with a high antioxidant blueberry extract. Here, we studied whether neurons were an important target of blueberry extract and whether the mechanism involved altered ROS signaling through MAP kinase and cyclic-AMP response element binding protein (CREB), pathways known to be activated in response to amyloid-beta (A beta). Primary hippocampal neurons were isolated and cultured from embryonic, middle-age or old-age (24 months) rats. Blueberry extract was found to be equally neuroprotective against A beta neurotoxicity at all ages. Increases in A beta toxicity with age were associated with age-related increases in immunoreactivity of neurons to pERK and an age-independent increase in pCREB. Treatment with blueberry extract strongly inhibited these increases in parallel with neuroprotection. Simultaneous labeling for ROS and for glutathione with dichlorofluorescein and monochlorobimane showed a mechanism of action of blueberry extract to involve transient ROS generation with an increase in the redox buffer glutathione. We conclude that the increased age-related susceptibility of old-age neurons to A beta toxicity may be due to higher levels of activation of pERK and pCREB pathways that can be protected by blueberry extract through inhibition of both these pathways through an ROS stress response. These results suggest that the beneficial effects of blueberry extract may involve transient stress signaling and ROS protection that may translate into improved cognition in aging rats and APP/PS1 mice given blueberry extract. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:991 / 998
页数:8
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