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Clas Blomberg - Physics of life-Elsevier Science (2007)

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346 Part VIII. Applications

The next important stage appears when a pulse reaches a connection to another nerve

cell, a synapse. There, the electric pulse is converted to a chemical pulse which is transferred

to the neighbouring synapse. In this, also calcium ions are involved. At the synapse,

the electric ion pulse is converted to a chemical signal that influences an adjacent neuron

cell. It may give rise to an electric pulse in the new cell by, for instance opening of sodium

channels. In other synapses, the influence may be the opposite, a signal can inhibit activity

in the adjacent neuron.

What happens in a cell depends on the combined action of connecting synapses, taking

into account excitatory and inhibitory tendencies with varying strengths. This is the basis

for models of neural networks. There nerve cells are considered as parts in a network connected

to other cells via excitatory and inhibitory synapses. An excitation in one cell can

generate new excitations (nerve signals in the connected cells by excitatory synapses and

absence of inhibitory ones). The inhibitory synapses are crucial to prevent exited nerve

pulses to spread over all nerve cells.

In the model neural network, the nerve cells are centres which are excited, with moving

pulses of the described type or silent, resting. These influence other cells by the synapses

of different characters and different strengths, and thus excite new cells or prevent excitation.

It is common here to regard the cells of various types in different layers to produce

certain propagation of excitation in the network. In that way, new cells (centres are excited,

and also inhibited), eventually lead to a stationary pattern where cells cannot excite or

inhibit further cells (Wilson and Cowan, 1972).

A common view is that such a resulting stationary pattern of excited cells can be apprehended

as “memories” of a certain stimulus, a basic input as pulse generation of certain cells.

Such a pattern can be generated again by the same or a very similar stimulus—in order to

retrieve a certain memory, all details must not be present. By slower connections patterns of

this kind can be further transferred and associated with other memory patterns—there is a

kind of associative network (Kohonen, 1987, Kleinfeld, D. and Sompolinsky, H., 1989).

The common view is also that here is a mechanism, that the network when influenced by

various stimuli can modify the synapse strengths in order to provide stronger stationary patterns,

stronger possible memories. These modifications of the synapses are then considered

as parts of a “learning” procedure, a way to “learn the system features of an original stimulus

and to provide stronger and more easily retrieved memories” (Levy and Steward, 1979).

The number of possible “memories” in this kind of network is much larger than the number

of network centres, of nerve cells. And as the number of cells in the brain is very large

and further the number of synapses, connections of each cell also is large, the possibilities

of a neural network are very large (Levy, 1985, Alexander and Moron, 1991).

32B

Spin-glass analogy

Hopfield (1982) described an interesting analogy to a kind of magnetic model, the spinglass

model, in order to accomplish a basis for the characterisation of a neural network.

Although not really correct in its details, this work opened, in particular among physicists,

important parts of this field and clarified basic concepts. See, e.g. the book on spin glasses

and applications by Mezard et al. (1987).

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