Coordinatore | FOUNDATION FOR RESEARCH AND TECHNOLOGY HELLAS
Organization address
address: N PLASTIRA STR 100 contact info |
Nazionalità Coordinatore | Greece [EL] |
Totale costo | 204˙141 € |
EC contributo | 204˙141 € |
Programma | FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) |
Code Call | FP7-PEOPLE-2007-4-1-IOF |
Funding Scheme | MC-IOF |
Anno di inizio | 2008 |
Periodo (anno-mese-giorno) | 2008-03-01 - 2010-02-28 |
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FOUNDATION FOR RESEARCH AND TECHNOLOGY HELLAS
Organization address
address: N PLASTIRA STR 100 contact info |
EL (HERAKLION) | coordinator | 0.00 |
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'Aging-induced memory deficiencies are caused by dysfunctions of various brain regions, including the hippocampus and the prefrontal cortex. Currently not much is known about the anatomical and biophysical properties or the underlying molecular mechanisms that enable these regions to contribute to memory formation or the effects of aging on neural learning and storage capacity. In this project, we propose to combine electrophysiological and modeling approaches to address issues pertaining to aging induced changes in cellular properties and how these influence the information processing capacity of hippocampal and neocortical cells. Towards this target, we will first perform electrophysiological experiments to characterize the intrinsic properties of young and aged pyramidal neurons and then use the accumulated as well as existing data to build realistic compartmental models of these cells. Models will incorporate both anatomical and biophysical information and will be used in simulation experiments to study the effects of aging on the excitability and integrative properties of hippocampal and neocortical neurons. We are especially interested in (a) investigating the ability of aged neurons to support nonlinear dendritic integration and process incoming signals like multi-layer neural networks and (b) identifying key mechanisms that influence dendritic integration properties as they may serve as a basis for new medical interventions that can alleviate memory loss in the elderly.'
Loss of memory brought on by ageing is the result of various dysfunctions in certain regions of the brain. Two of these areas are the hippocampus and the prefrontal cortex.
Knowledge is still at a rather rudimentary level with regard to the anatomical and biophysical properties, or underlying molecular processes, which support and promote the formation of memory. This is also true in relation to the effects of ageing on neural learning and ability to retain information.
The 'Computational modeling and physiological studies of neural form and function in the aging brain' (Anamnisis) project focused on ageing-induced changes in cellular properties and how these affect the ability of hippocampal and neocortical cells to process information. To do this, the EU-funded project combined electrophysiological and modelling approaches.
Software was developed for analyses of planned electrophysiological recordings aimed at characterising the properties of young and aged pyramidal neurons. Data retrieved from these experiments enabled team members to refine young and aged pyramidal neuron models. Pyramidal neurons are pyramidal-shaped bodies of cells commonly found in forebrain structures; they are thought to play an important role in advanced cognitive functions. Success in this area facilitated investigation of the role of morphological alterations in specific properties of certain aged pyramidal neurons.
Anamnisis researchers focused on gathering anatomical and biophysical information for use in simulation experiments so as to study how ageing affects the excitability and integrative properties of hippocampal and neocortical neurons.
Projects results aimed to contribute knowledge on the key mechanisms influencing integration properties of dendrites. Advances in this area have the potential to drive new medical interventions that can lessen the effects of memory loss in the elderly.