Inhibitory Neuron and Hippocampal Circuit Dysfunction in an Aged Mouse Model of Alzheimer's Disease

被引:68
|
作者
Hazra, Anupam [1 ]
Gu, Feng [1 ]
Aulakh, Ahmad [1 ]
Berridge, Casey [2 ]
Eriksen, Jason L. [2 ]
Ziburkus, Jokubas [1 ]
机构
[1] Univ Houston, Dept Biol & Biochem, Houston, TX USA
[2] Univ Houston, Dept Pharmacol & Pharmaceut Sci, Houston, TX 77204 USA
来源
PLOS ONE | 2013年 / 8卷 / 05期
基金
美国国家卫生研究院;
关键词
PAIRED HELICAL FILAMENTS; PROTEIN-TAU TAU; AMYLOID-BETA; COGNITIVE IMPAIRMENTS; DENTATE GYRUS; EPILEPSY; CALCIUM; SEIZURES; PLAQUES; NETWORK;
D O I
10.1371/journal.pone.0064318
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In Alzheimer's disease (AD), a decline in explicit memory is one of the earliest signs of disease and is associated with hippocampal dysfunction. Amyloid protein exerts a disruptive impact on neuronal function, but the specific effects on hippocampal network activity are not well known. In this study, fast voltage-sensitive dye imaging and extracellular and whole-cell electrophysiology were used on entorhinal cortical-hippocampal slice preparations to characterize hippocampal network activity in 12-16 month old female APPswe/PSEN1DeltaE9 (APdE9 mice) mice. Aged APdE9 mice exhibited profound disruptions in dentate gyrus circuit activation. High frequency stimulation of the perforant pathway in the dentate gyrus (DG) area of APdE9 mouse tissue evoked abnormally large field potential responses corresponding to the wider neural activation maps. Whole-cell patch clamp recordings of the identified inhibitory interneurons in the molecular layer of DG revealed that they fail to reliably fire action potentials. Taken together, abnormal DG excitability and an inhibitory neuron failure to generate action potentials are suggested to be important contributors to the underlying cellular mechanisms of early-stage Alzheimer's disease pathophysiology.
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页数:9
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