Neuronal-Based Synaptic Compensation: A Computational Study in Alzheimer's Disease

In the framework of an associative memory model, we study the interplay between synaptic deletion and compensation, and memory deterioration, a clinical hallmark of Alzheimer's disease. Our study is motivated by experimental evidence that there are regulatory mechanisms that take part in the homeostasis of neuronal activity and act on the neuronal level. We show that following synaptic deletion, synaptic compensation can be carried out efficiently by a local, dynamic mechanism, where each neuron maintains the profile of its incoming post-synaptic current. Our results open up the possibility that the primary factor in the pathogenesis of cognitive deficiencies in Alzheimer's disease (AD) is the failure of local neuronal regulatory mechanisms. Allowing for neuronal death, we observe two pathological routes in AD, leading to different correlations between the levels of structural damage and functional decline.

[1]  D. Salmon,et al.  Physical basis of cognitive alterations in alzheimer's disease: Synapse loss is the major correlate of cognitive impairment , 1991, Annals of neurology.

[2]  Bradley T. Hyman,et al.  Neurofibrillary tangles but not senile plaques parallel duration and severity of Alzheimer's disease , 1992, Neurology.

[3]  S. B. Kater,et al.  Excitatory and inhibitory neurotransmitters in the generation and degeneration of hippocampal neuroarchitecture , 1989, Brain Research.

[4]  M. Montminy,et al.  Transsynaptic control of gene expression. , 1993, Annual review of neuroscience.

[5]  B. Horwitz,et al.  Volumetric magnetic resonance imaging in men with dementia of the Alzheimer type: Correlations with disease severity , 1993, Biological Psychiatry.

[6]  Eytan Ruppin,et al.  Compensatory Mechanisms in an Attractor Neural Network Model of Schizophrenia , 1995, Neural Computation.

[7]  Carl W. Cotman,et al.  The Role of Misdirected Plasticity in Plaque Biogenesis and Alzheimer's Disease Pathology , 1991 .

[8]  E. Marder,et al.  Activity-dependent changes in the intrinsic properties of cultured neurons. , 1994, Science.

[9]  L. F. Abbott,et al.  Analysis of Neuron Models with Dynamically Regulated Conductances , 1993, Neural Computation.

[10]  A. V. Ooyen,et al.  Activity-dependent outgrowth of neurons and overshoot phenomena in developing neural networks , 1994 .

[11]  E. Masliah,et al.  Increase of synaptic density and memory retention by a peptide representing the trophic domain of the amyloid beta/A4 protein precursor. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[12]  Iain P. Chessell,et al.  Neurotransmission—the link integrating Alzheimer research? , 1994, Trends in Neurosciences.

[13]  E. Marder,et al.  Activity-dependent regulation of conductances in model neurons. , 1993, Science.

[14]  S. DeKosky,et al.  Synapse loss in frontal cortex biopsies in Alzheimer's disease: Correlation with cognitive severity , 1990, Annals of neurology.

[15]  P. Coleman,et al.  Dendritic growth in the aged human brain and failure of growth in senile dementia. , 1979, Science.

[16]  N Butters,et al.  Clinical correlates of cortical and nucleus basalis pathology in Alzheimer dementia. , 1994, Archives of neurology.

[17]  J A Reggia,et al.  A Neural Model of Memory Impairment in Di(cid:11)use Cerebral Atrophy , 2004 .

[18]  J. Duchek,et al.  Senile dementia and healthy aging: a longitudinal CT study. , 1991, Radiology.

[19]  M. Dickinson,et al.  Electrical activity in cerebellar cultures determines Purkinje cell dendritic growth patterns , 1991, Neuron.

[20]  D. Selkoe,et al.  Normal and abnormal biology of the beta-amyloid precursor protein. , 1994, Annual review of neuroscience.

[21]  W. Meier-Ruge,et al.  Quantitative morphology of synaptic plasticity in the aging brain. , 1988, Scanning microscopy.

[22]  T. Curran,et al.  Stimulus-transcription coupling in the nervous system: involvement of the inducible proto-oncogenes fos and jun. , 1991, Annual review of neuroscience.

[23]  R. Katzman.,et al.  Senile Dementia of the Alzheimer Type Without Neocortical Neurofibrillary Tangles , 1987, Journal of neuropathology and experimental neurology.

[24]  H. C. LONGUET-HIGGINS,et al.  Non-Holographic Associative Memory , 1969, Nature.

[25]  E. Masliah,et al.  Mechanisms of synaptic dysfunction in Alzheimer's disease. , 1995, Histology and histopathology.

[26]  E. Masliah,et al.  Synaptic and neuritic alterations during the progression of Alzheimer's disease , 1994, Neuroscience Letters.

[27]  Michael Alford,et al.  Patterns of aberrant sprouting in alzheimer's disease , 1991, Neuron.

[28]  K. Kosik,et al.  Neuritic pathology and dementia in alzheimer's disease , 1991, Annals of neurology.

[29]  P. Coleman,et al.  Failed Compensatory Dendritic Growth as a Pathophysiological Process in Alzheimer's Disease , 1986, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[30]  A. V. Ooyen Activity-dependent neural network development , 1994 .

[31]  D. Price,et al.  Synapse loss in the temporal lobe in Alzheimer's disease , 1993, Annals of neurology.

[32]  M. Tsodyks,et al.  The Enhanced Storage Capacity in Neural Networks with Low Activity Level , 1988 .

[33]  Leif H. Finkel,et al.  Neuromodulatory control of hippocampal function: towards a model of Alzheimer's disease , 1998, Artif. Intell. Medicine.

[34]  B Carragher,et al.  Three-Dimensional Analysis of the Relationship Between Synaptic Pathology and Neuropil Threads in Alzheimer Disease , 1992, Journal of neuropathology and experimental neurology.

[35]  W. Meier-Ruge,et al.  Morphological adaptive response of the synaptic junctional zones in the human dentate gyrus during aging and Alzheimer's disease , 1990, Brain Research.

[36]  F. Gage,et al.  Synaptic loss in cognitively impaired aged rats is ameliorated by chronic human nerve growth factor infusion , 1995, Neuroscience.

[37]  Marius Usher,et al.  Neural Network Modeling of Memory Deterioration in Alzheimer's Disease , 1993, Neural Computation.

[38]  J. Nicholls,et al.  Influence of substrate on retraction of neurites following electrical activity of leech Retzius cells in culture. , 1992, The Journal of experimental biology.

[39]  Eytan Ruppin,et al.  Memory Maintenance via Neuronal Regulation , 1998, Neural Computation.

[40]  C. Cotman,et al.  Synaptic plasticity and functional stabilization in the hippocampal formation: possible role in Alzheimer's disease. , 1988, Advances in neurology.

[41]  M. Tabaton,et al.  Neuropil threads of Alzheimer's disease show a marked alteration of the normal cytoskeleton , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[42]  B. Sakmann,et al.  Active propagation of somatic action potentials into neocortical pyramidal cell dendrites , 1994, Nature.

[43]  C. Barnes Normal aging: regionally specific changes in hippocampal synaptic transmission , 1994, Trends in Neurosciences.