Cognitive Science 201A
Neuroanatomy and Neurophysiology

Name: _________________________

HOMEWORK #1:

Checklist:
  (a) due by Wednesday 10/18/00, under my door (CSB 171)
  (b) use this page as the first page
  (c) staple all pages together
  (d) one page maximum per answer (less than a page is better!)
  (e) each answer on a separate page
  (f) figures on same page as answer
  (g) word-processor text with hand-drawn figures preferred

1. A cell has channels that only conduct a singly-charged positive ion. Assume that these channels are opened momentarily with the cell at rest (assume resting membrane potential is about -70 mv). Indicate (a) which way the ions will flow (if at all), and (b) how this will affect the membrane potential, for the following three intracellular and extracellular concentrations of this ion:

inside: 120 mM    outside: 120 mM
inside: 36 mM     outside: 7.4 mM
inside: 41 mM     outside: 1.3 mM
Then indicate (c) which way the ions will flow in the three concentrations when the membrane potential is first clamped to about -40 mv with a voltage clamp and the channels are then momentarily opened.

2. Backpropagation is a technique for assigning error to weights in one or more hidden layers. What exact feature of this algorithm is hard to implement in real neural circuits? (be specific--this means you have to briefly describe how backprop works). Neurons in one part of the brain often project to another part of the brain as a topographic map. How does this differ from the networks typically used in cognitive models?

3. Ionic current flows at synapses made onto dendrites generate electric potentials that take considerable time (milliseconds) to propagate down to the cell body, despite the fact that changes in intracellular potentials are conducted through cellular fluids virtually instantaneously. Explain why this is by considering what happens when a current step--a sudden and continuously maintained increase in current--is injected into one location on a dendrite. First draw a simple circuit diagram of a dendrite. Then qualitatively describe the three different kinds of current flows (capacitive, transmembrane resistive, longitudinal resistive) current flows in the dendrite at three different points in time (before the current went on, soon after the current went on, and a long time after the current went on) and at two different spatial locations (near the injection site, and far from the injection site). To reiterate, this means you should mention a total of 18 things (3 currents x 3 times x 2 places).

4. Explain briefly how NMDA channels at a synapse detect correlations between the activity in the pre- and post-synaptic cells. In class we talked mainly about the involvement of NMDA channels in LTP, which has often been studied in the hippocampus. In the neocortex, in contrast to the hippocampus, the voltage-sensitive current passing through NMDA channels contributes significantly to post-synaptic potential. In light of this piece of information, describe how, in the absence of LTP, the excitatory voltage-sensitive NMDA current can allow a particular synapse to have different effective synaptic weights at different times (describe two different situations involving the same synapse)

5. (a) Why does the Linsker update equation contain only pre-synaptic terms given that a Hebb rule is typically described as changing the weight according to the correlation of pre- and post-synaptic activity? (b) Give three examples of 5 pairs of activation values for two units that illustrate positive, negative, and zero correlation (c) Why do the weights from input units in the center of the receptive field of a higher-layer unit increase faster than weights in the periphery of the same receptive field when there is a Gaussian 2-point correlation between input layer units? (d) Explain how how Linsker learning rule can be thought of as a matrix operating on a vector to yield another vector (say explicitly what the input and output vectors are, and what the matrix consists of).

6. The diagram below shows a simple fully-connected Hopfield network with 4 units (present state of each unit is shown inside of it) and 12 weights (smaller numbers). Using the update and energy equations given in class, determine: (a) what the present 'energy' of the network is, (b) whether the network is now in a stable state, and (c) what the energy will be after each unit in network has been asynchronously updated once (left to right). This weight matrix is not symmetric. (d) Very briefly, why is a symmetric weight (connection) matrix required for the proof that no single unit update can ever increase the energy?


7. In class, we considered a single-compartment integrate-and-fire model described in Wilson and Bower (1989). (a) What are the processes in real neurons are that are summarized by the alpha function (conductance function for one channel type)? (b) Draw the equivalent electrical circuit for a single neuron with one sodium and one chloride channel attached to it. (c) Assume that an excitatory synaptic input to a neuron is activated just before a GABA-A input to the same neuron. Would the GABA-A channel conduct more, the same, or less current than in the situation where it is activated by itself? Explain your answer by giving a qualitative discussion of the relevant equation. (d) Since a convolution is used to sum up the effect of inputs at one connection, linear superposition of conductances is assumed. Describe a situation (there are many possibilities!) in a real neuron where linear superposition at a connection would not hold.

8. Make diagrams of the normal connections of the two retinas with the two dorsal lateral geniculate nuclei in the cat and an Old World primate (N.B.: the dLGN's of cats and primates are different!). Diagram how are these connections are changed in the mutant Belgian sheepdog (the non-mutant sheepdog has a cat-like dLGN). What does this mutant seem to imply about mechanisms thought to be involved in stabilization of connections in the developing nervous system (e.g., correlated activity, map- position-dependent biochemical markers)? Give an example from the readings that comes to the opposite conclusion.