Title :
Effects of Alzheimer´s pathology on memory function in a biophysical model of hippocampal CA3
Author :
Finkel, Leif H. ; Menschik, Elliot D.
Author_Institution :
Dept. of Bioeng., Pennsylvania Univ., Philadelphia, PA, USA
Abstract :
Among the pathological hallmarks of Alzheimer´s disease (AD) are cholinergic deprivation and extracellular plaques comprised the amyloid β-peptide (Aβ). Here their effects on cellular neurophysiology and network autoassociative function are assessed in a simulation of hippocampal area CA3 comprised of biophysical cellular models. Cholinergic denervation is found to slow the intrinsic gamma rhythm of the network, resulting in fewer iterations to converge to stored memory patterns. Acetylcholine (ACh) modulates the firing mode of pyramidal cells from bursting to regular spiking and leads to concomitant changes in dendritic calcium levels. In addition, our simulation of the reported blockade of KA channels by Aβ leads a similar transition in firing mode but increased dendritic calcium accumulation relative to ACh
Keywords :
brain models; cellular biophysics; diseases; neural nets; neurophysiology; Alzheimer´s disease; Alzheimer´s pathology effects; Ca; K; acetylcholine; amyloid β-peptide; biophysical model; cellular neurophysiology; cholinergic denervation; cholinergic deprivation; extracellular plaques; hippocampal CA3; hippocampal area CA3 simulation; intrinsic gamma rhythm; network autoassociative function; pathological hallmarks; pyramidal cells firing mode; stored memory patterns; Alzheimer´s disease; Biomedical engineering; Calcium; Cellular networks; Frequency synchronization; Neurophysiology; Pathology; Rhythm; Robustness; Testing;
Conference_Titel :
[Engineering in Medicine and Biology, 1999. 21st Annual Conference and the 1999 Annual Fall Meetring of the Biomedical Engineering Society] BMES/EMBS Conference, 1999. Proceedings of the First Joint
Conference_Location :
Atlanta, GA
Print_ISBN :
0-7803-5674-8
DOI :
10.1109/IEMBS.1999.804349