Neural cytoskeleton capabilities for learning and memory

This paper proposes a physical model involving the key structures within the neural cytoskeleton as major players in molecular-level processing of information required for learning and memory storage. In particular, actin filaments and microtubules are macromolecules having highly charged surfaces that enable them to conduct electric signals. The biophysical properties of these filaments relevant to the conduction of ionic current include a condensation of counterions on the filament surface and a nonlinear complex physical structure conducive to the generation of modulated waves. Cytoskeletal filaments are often directly connected with both ionotropic and metabotropic types of membrane-embedded receptors, thereby linking synaptic inputs to intracellular functions. Possible roles for cable-like, conductive filaments in neurons include intracellular information processing, regulating developmental plasticity, and mediating transport. The cytoskeletal proteins form a complex network capable of emergent information processing, and they stand to intervene between inputs to and outputs from neurons. In this manner, the cytoskeletal matrix is proposed to work with neuronal membrane and its intrinsic components (e.g., ion channels, scaffolding proteins, and adaptor proteins), especially at sites of synaptic contacts and spines. An information processing model based on cytoskeletal networks is proposed that may underlie certain types of learning and memory

Neural computation of visual imaging based on Kronecker product in the primary visual cortex

Background: What kind of neural computation is actually performed by the primary visual cortex and how is this represented mathematically at the system level? It is an important problem in the visual information processing, but has not been well answered. In this paper, according to our understanding of retinal organization and parallel multi-channel topographical mapping between retina and primary visual cortex V1, we divide an image into orthogonal and orderly array of image primitives (or patches), in which each patch will evoke activities of simple cells in V1. From viewpoint of information processing, this activated process, essentially, involves optimal detection and optimal matching of receptive fields of simple cells with features contained in image patches. For the reconstruction of the visual image in the visual cortex V1 based on the principle of minimum mean squares error, it is natural to use the inner product expression in neural computation, which then is transformed into matrix form. Results: The inner product is carried out by using Kronecker product between patches and function architecture (or functional column) in localized and oriented neural computing. Compared with Fourier Transform, the mathematical description of Kronecker product is simple and intuitive, so is the algorithm more suitable for neural computation of visual cortex V1. Results of computer simulation based on two-dimensional Gabor pyramid wavelets show that the theoretical analysis and the proposed model are reasonable. Conclusions: Our results are: 1. The neural computation of the retinal image in cortex V1 can be expressed to Kronecker product operation and its matrix form, this algorithm is implemented by the inner operation between retinal image primitives and primary visual cortex's column. It has simple, efficient and robust features, which is, therefore, such a neural algorithm, which can be completed by biological vision. 2. It is more suitable that the function of cortical column in cortex V1 is considered as the basic unit of visual image processing (such unit can implement basic multiplication of visual primitives, such as contour, line, and edge), rather than a set of tiled array filter. Fourier Transformation is replaced with Kronecker product, which greatly reduces the computational complexity. The neurobiological basis of this idea is that a visual image can be represented as a linear combination of orderly orthogonal primitive image containing some local feature. In the visual pathway, the image patches are topographically mapped onto cortex V1 through parallel multi-channels and then are processed independently by functional columns. Clearly, the above new perspective has some reference significance to exploring the neural mechanisms on the human visual information processing.http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000277524600002&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701NeurosciencesSCI(E)0ARTICLEnull1

A Unified Cognitive Model of Visual Filling-In Based on an Emergic Network Architecture

The Emergic Cognitive Model (ECM) is a unified computational model of visual filling-in based on the Emergic Network architecture. The Emergic Network was designed to help realize systems undergoing continuous change. In this thesis, eight different filling-in phenomena are demonstrated under a regime of continuous eye movement (and under static eye conditions as well). ECM indirectly demonstrates the power of unification inherent with Emergic Networks when cognition is decomposed according to finer-grained functions supporting change. These can interact to raise additional emergent behaviours via cognitive re-use, hence the Emergic prefix throughout. Nevertheless, the model is robust and parameter free. Differential re-use occurs in the nature of model interaction with a particular testing paradigm. ECM has a novel decomposition due to the requirements of handling motion and of supporting unified modelling via finer functional grains. The breadth of phenomenal behaviour covered is largely to lend credence to our novel decomposition. The Emergic Network architecture is a hybrid between classical connectionism and classical computationalism that facilitates the construction of unified cognitive models. It helps cutting up of functionalism into finer-grains distributed over space (by harnessing massive recurrence) and over time (by harnessing continuous change), yet simplifies by using standard computer code to focus on the interaction of information flows. Thus while the structure of the network looks neurocentric, the dynamics are best understood in flowcentric terms. Surprisingly, dynamic system analysis (as usually understood) is not involved. An Emergic Network is engineered much like straightforward software or hardware systems that deal with continuously varying inputs. Ultimately, this thesis addresses the problem of reduction and induction over complex systems, and the Emergic Network architecture is merely a tool to assist in this epistemic endeavour. ECM is strictly a sensory model and apart from perception, yet it is informed by phenomenology. It addresses the attribution problem of how much of a phenomenon is best explained at a sensory level of analysis, rather than at a perceptual one. As the causal information flows are stable under eye movement, we hypothesize that they are the locus of consciousness, howsoever it is ultimately realized

Work Toward a Theory of Brain Function

This dissertation reports research from 1971 to the present, performed in three parts. The first part arose from unilateral electrical stimulation of motivational/reward pathways in the lateral hypothalamus and brain stem of “split-brain” cats, in which the great cerebral commissures were surgically divided. This showed that motivation systems in split-brain animals exert joint influence upon learning in both of the divided cerebral hemispheres, in contrast to the separation of cognitive functions produced by commissurotomy. However, attempts to identify separate signatures of electrocortical activity associated with the diffuse motivational/alerting effects and those of the cortically lateralised processes failed to achieve this goal, and showed that an adequate model of cerebral information processing was lacking. The second part describes how this recognition of inadequacy led into computer simulations of large populations of cortical neurons – work which slowly led my colleagues and me to successful explanations of mechanisms for cortical synchrony and oscillation, and of evoked potentials and the global EEG. These results complemented the work of overseas groups led by Nunez, by Freeman, by Lopes da Silva and others, but also differed from the directions taken by these workers in certain important respects. It became possible to conceive of information transfer in the active cortex as a series of punctuated synchronous equilibria of signal exchange among cortical neurons – equilibria reached repeatedly, with sequential perturbations of the neural activity away from equilibrium caused by exogenous inputs and endogenous pulse-bursting, thus forming a basis for cognitive sequences. The third part reports how the explanation of synchrony gave rise to a new theory of the regulation of embryonic cortical growth and the emergence of mature functional connections. This work was based upon very different assumptions, and reaches very different conclusions, to that of pioneers of the field such as Hubel and Wiesel, whose ideas have dominated cortical physiology for more than fifty years. In conclusion, findings from all the stages of this research are linked together, to show they provide a sketch of the working brain, fitting within and helping to unify wider contemporary concepts of brain function