Literature DB >> 25879152

A mouse model of Alzheimer's disease displays increased susceptibility to kindling and seizure-associated death.

Jianxiong Chan1, Nigel C Jones1, Ashley I Bush2, Terence J O'Brien1,3, Patrick Kwan1,3.   

Abstract

People with Alzheimer's disease (AD) are up to 10 times more likely to develop epilepsy than the age-matched general population. However, given that only a proportion of patients with AD develop epilepsy, it is likely that additional factors may be required for the epilepsy to emerge. This study aimed to better understand the relationship between AD pathology and seizure susceptibility. It also aimed to investigate a "two-hit" hypothesis for seizure susceptibility through amygdala kindling of rodent AD models. Aged AD mice (Tg2576 model) and wild-type (WT) mice underwent electrical amygdala kindling. Compared with WT mice, Tg2576 mice had significantly lower afterdischarge threshold. Significantly fewer stimulations were required for the Tg2576 mice to reach the first class V seizure. Higher death rate was observed with Tg2576 mice in the kindling group. Both sham and kindled Tg2576 animals had increased levels of sprouting in the supragranular layer of the dentate gyrus compared with the WT counterparts. These findings support the "two-hit" hypothesis and represent a potentially novel research model to help better understand the relationship between AD pathology and epilepsy. Wiley Periodicals, Inc.
© 2015 International League Against Epilepsy.

Entities:  

Keywords:  Alzheimer's disease; Amygdala kindling; Epilepsy; Seizure death; Tg2576

Mesh:

Substances:

Year:  2015        PMID: 25879152     DOI: 10.1111/epi.12993

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  12 in total

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Authors:  Amanda M Gleixner; Jessica M Posimo; Deepti B Pant; Matthew P Henderson; Rehana K Leak
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2.  Genetic ablation of the p66Shc adaptor protein reverses cognitive deficits and improves mitochondrial function in an APP transgenic mouse model of Alzheimer's disease.

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3.  Neuronal Network Excitability in Alzheimer's Disease: The Puzzle of Similar versus Divergent Roles of Amyloid β and Tau.

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Journal:  eNeuro       Date:  2021-04-23

Review 4.  What goes up must come down: homeostatic synaptic plasticity strategies in neurological disease.

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Journal:  Future Neurol       Date:  2018-01-17

5.  Inflammasome-derived cytokine IL18 suppresses amyloid-induced seizures in Alzheimer-prone mice.

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Journal:  Proc Natl Acad Sci U S A       Date:  2018-08-20       Impact factor: 11.205

6.  Synergistic stress exacerbation in hippocampal neurons: Evidence favoring the dual-hit hypothesis of neurodegeneration.

Authors:  Scott D Heinemann; Jessica M Posimo; Daniel M Mason; Daniel F Hutchison; Rehana K Leak
Journal:  Hippocampus       Date:  2016-03-29       Impact factor: 3.899

Review 7.  The basolateral amygdala γ-aminobutyric acidergic system in health and disease.

Authors:  Eric M Prager; Hadley C Bergstrom; Gary H Wynn; Maria F M Braga
Journal:  J Neurosci Res       Date:  2015-11-19       Impact factor: 4.164

Review 8.  Dementia in Down syndrome: unique insights for Alzheimer disease research.

Authors:  Ira T Lott; Elizabeth Head
Journal:  Nat Rev Neurol       Date:  2019-03       Impact factor: 42.937

9.  Superimposing Status Epilepticus on Neuron Subset-Specific PTEN Haploinsufficient and Wild Type Mice Results in Long-term Changes in Behavior.

Authors:  Gregory D Smith; Jessika White; Joaquin N Lugo
Journal:  Sci Rep       Date:  2016-11-07       Impact factor: 4.379

Review 10.  Revisiting the Impact of Neurodegenerative Proteins in Epilepsy: Focus on Alpha-Synuclein, Beta-Amyloid, and Tau.

Authors:  Yam Nath Paudel; Efthalia Angelopoulou; Christina Piperi; Iekhsan Othman; Mohd Farooq Shaikh
Journal:  Biology (Basel)       Date:  2020-06-12
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