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Mice With Alzheimer's Disease Suffer 'Silent' Seizures

Date:
September 9, 2007
Source:
Baylor College of Medicine
Summary:
Mice genetically engineered to have a disease like Alzheimer's have "silent" seizures that appear related to cellular changes involving the excess accumulations of the protein amyloid beta, said researchers.
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Mice genetically engineered to have a disease like Alzheimer's have "silent" seizures that appear related to cellular changes involving the excess accumulations of the protein amyloid beta, said researchers from the Gladstone Institute of Neurological Disease and Baylor College of Medicine in a report that appears in the journal Neuron.

"These seizures are not the typical epileptic seizures or convulsions that most people would recognize," said Dr. Jeffrey Noebels, BCM professor of neurology, neuroscience and molecular and human genetics and a co-senior author of the report. "These episodes may be the reason that some people with advanced Alzheimer's disease have 'spells' of increased confusion. Further study of this mouse may offer new ways to prevent these episodes."

Noebels recorded electrical brain waves deep in the brain of these special mice in the Bluebird Circle Developmental Neurogenetics Laboratory at BCM. The activity was detected in the brain's hippocampus, an area important in memory.

"This discovery has helped identify a new and potentially reversible neural mechanism that can explain the episodes of sudden severe confusion found in cases of advanced Alzheimer's disease," said Noebels.

"The cellular changes that give rise to this hyperexcitability appear slowly as the disease progresses, and at a certain point, the brain networks actually become hyperexcitable, despite the loss of synapses and brain cells in this brain region. Further study may point to early treatment that might prevent these electrical brain spells, as well as slow down the progression of this debilitating disease."

"Such abnormal network activity in Alzheimer's patients was thought to be a collateral or secondary event caused by the degeneration of nerve cells," said Dr. Jorge Palop, the study's lead author and a Gladstone research scientist. "But our study suggests that this activity may actually be a primary effect of amyloid beta and an early determinant of cognitive failure."

Amyloid beta is a toxic protein fragment found in the brains of people with Alzheimer's and similar disorders.

"Our results have important therapeutic implications, because the prevention and reversal of non-convulsive seizure activity has not yet been a major focus of clinical trials in Alzheimer's disease. Our results suggest that the suppression of this activity might prevent and possibly even reverse cognitive impairments induced by high levels of amyloid beta," said Dr. Leonard Muecke, co-senior author, professor of neurology at the University of California San Francisco and director of the Gladstone Institute.

The mice were genetically engineered by Palop, Muecke and their team. Others who took part in the research include Jeannie Chin, Erik Roberson, Jun Wang, Myo Thwin, Nga Bien-Ly, Jong Yoo, Kaitlyn Ho, Gui-Qiu Yu, Anatol Kreitzer and Steven Finkbeiner, all of Gladstone.

Reference: Palop et al.: "Aberrant Excitatory Neuronal Activity and Compensatory Remodeling of Inhibitory Hippocampal Circuits in Mouse Models of Alzheimer's Disease." Publishing in Neuron 55, 697--711, September 6, 2007. DOI 10.1016/j.neuron.2007.07.025.

Funding for this work came from the National Institutes of Health and the McBean Foundation.


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Baylor College of Medicine. "Mice With Alzheimer's Disease Suffer 'Silent' Seizures." ScienceDaily. ScienceDaily, 9 September 2007. <www.sciencedaily.com/releases/2007/09/070905123908.htm>.
Baylor College of Medicine. (2007, September 9). Mice With Alzheimer's Disease Suffer 'Silent' Seizures. ScienceDaily. Retrieved May 23, 2017 from www.sciencedaily.com/releases/2007/09/070905123908.htm
Baylor College of Medicine. "Mice With Alzheimer's Disease Suffer 'Silent' Seizures." ScienceDaily. www.sciencedaily.com/releases/2007/09/070905123908.htm (accessed May 23, 2017).

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