High-order behaviour in learning gate networks with lateral inhibition
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Abstract
In this work we present a neural network model incorporating activity-dependent presynaptic facilitation with multidimensional inputs. The processing unit used is based on a slightly simplified version of the Learning Gate Model proposed by Ciaccia et al. (1992). The network topology integrates a well-known biological neural circuit with a lateral inhibition connection subnet. By means of simulation experiments, we show that the proposed networks exhibit basic and high-order features of associative learning. In particular, overshadowing and blocking are reproduced in the presence of both noise-free and noisy inputs. The role of noise in the development of high-order learning capabilities is also discussed.
Keywords
Network Model Network Topology Simulation Experiment Processing Unit Neural Network ModelPreview
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References
- Bailey CH, Chen M (1988) Long-term memory in Aplysia modulates the total number of varicosities of single identified sensory neurons. Proc Nat Acad Sci USA 85:2373–2377Google Scholar
- Buonomano DV, Byrne JH (1990) Long-term synaptic changes produced by a cellular analog of classical conditioning in Aplysia. Science 249:420–423Google Scholar
- Buonomano DV, Baxter DA, Byrne JH (1990) Small networks of empirically derived adaptive elements simulate some higher-order features of classical conditioning. Neural Networks 3:507–523Google Scholar
- Byrne JH (1987) Cellular analysis of associative learning. Physiol Rev 67:329–439Google Scholar
- Byrne JH, Eskin A, Scholz KP (1989) Neuronal mechanisms contributing to long-term sensitization in Aplysia. J Physiol 83:141–147Google Scholar
- Byrne JH, Baxter DA, Buonomano DV, Raymond JL (1990) Neuronal and network determinants of simple and higher-order features of associative learning: experimental and modeling approach. Cold Spring Harbor Symp Quant Biol 55:175–186Google Scholar
- Carpenter GA, Grossberg S (1990) ART3: Hierarchical search using chemical transmitters in self-organizing pattern recognition architectures. Neural Networks 3:129–152Google Scholar
- Castellucci VF, Kandel ER (1976) Presynaptic facilitation as a mechanism for behavioral sensitization in Aplysia. Science 94:1176–1178Google Scholar
- Ciaccia P, Maio D, Vacca GP (1992) An analytical short-and long-term memory model of presynaptic plasticity. Biol Cybern 67:335–345Google Scholar
- Gingrich KJ, Byrne JH (1985) Simulation of synaptic depression, posttetanic potentiation, and presynaptic facilitation of synaptic potentials from sensory neurons mediating gill-withdrawal in Aplysia. J Neurophysiol 53:652–669Google Scholar
- Gingrich KJ, Byrne JH (1987) Single-cell neuronal model for associative learning. J Neurophysiol 57:1705–1715Google Scholar
- Gingrich KJ, Baxter DA, Byrne JH (1988) Mathematical model of cellular mechanisms contributing to presynaptic facilitation. Brain Res Bull 21:513–520Google Scholar
- Gluck MA, Thompson RF (1987) Modeling the neural substrates of associative learning and memory: a computational approach. Psychol Rev 94:176–191Google Scholar
- Grossberg S, Levine DS (1987) Neural dynamics of attentionally modulated Pavlovian conditioning: blocking, interstimulus interval, and secondary reinforcement. Appl Optics 26:5015–5030Google Scholar
- Hawkins RD (1989a) A biologically based computational model for several simple forms of learning. In: Hawkins RD, Bower GH (eds) Computational models of learning in simple neural systems. Academic Press, San DiegoGoogle Scholar
- Hawkins RD (1989b) A biologically realistic neural network model for higher-order features of classical conditioning. In: Morris RGM (eds) Parallel distribuited processing, implications for psychology and neurology. Clarendon Press, OxfordGoogle Scholar
- Hawkins RD, Kandel ER (1984) Is there a cell-biological alphabet for simple forms of learning? Psychol Rev 91:375–391Google Scholar
- Hawkins RD, Abrams TW, Carew TJ, Kandel ER (1983) A cellular mechanism of classical conditioning in Aplysia: activity-dependent amplification of presynaptic facilitation. Science 219:400–405Google Scholar
- Kandel ER, Schwartz JH (1982) Molecular biology of learning: modulation of transmitter release. Science 218:433–443Google Scholar
- Kandel ER, Abrams TW, Bernier L, Carew TJ, Hawkins RD (1983) Classical conditioning and sensitization share aspects of same molecular cascade in Aplysia. Cold Spring Harbor Symp Quant Biol 48:821–830Google Scholar
- Kohonen T (1984) Self-organization and associative memory. Springer, Berlin Heidelberg New York.Google Scholar
- Mackintosh NJ (1974) The psychology of animal learning. Academic Press, LondonGoogle Scholar
- Rescorla RA, Wagner AR (1972) A theory of Pavlovian conditioning: variations in the effectiveness of reinforcement. In: Black AH, Prokasy VF (eds) Classical conditioning II: current research and theory. Appleton-Century-Crofts, New York, pp 64–99Google Scholar
- Small SA, Kandel ER, Hawkins RD (1989) Activity-dependent enhancement of presynaptic inhibition in Aplysia sensory neurons. Science 243:1603–1606Google Scholar
- Sutton RS, Barto AG (1990) Time-derivative models of Pavlovian reinforcement. In: Gabriel M, Moore JW (eds) Learning and computational neuroscience. MIT Press, Cambridge, Mass.Google Scholar
- Walters ET, Byrne JH (1983) Associative conditioning of single sensory neurons suggests a cellular mechanism for learning. Science 219:405–408Google Scholar
- Witt JC, Clark JW (1990) Experiments in artificial psychology: conditioning f asynchronous neural networks models. Math Biosci 99:77–104Google Scholar
- Yuille AL, Grzywacz NM (1993) A winner-take-all mechanism based on presynaptic inhibition feedback. Neural Comput 1:334–347Google Scholar