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Each culture sample was removed from the incubator for about 60 minutes, and each individual neuron test lasted about 40 minutes.

Figure 3 B shows a representative FEF neuron tested during sinusoidal SP and during fixation with visual stimulation.

The average changes induced by serotonin on spike latency and the first inter-spike interval for each neuron tested are illustrated in Fig. 3C.

We explored the optimum parameters for each neuron as follows: We first tested color selectivity using a certain shape (usually circle or the optimal shape for the neuron tested immediately before).

Inward rectification in the hyperpolarizing direction was present in 43 of the 79 neurons tested.

In 13% of the neurons tested, D1 receptor stimulation facilitated fornix-evoked responses.

On the other hand, administration of the selective D2 agonist quinpirole (10 μM) induced a hyperpolarization in six out of eight neurons tested.

Stressin I application, but not urocortin III, consistently initiated action potential discharge in all cholinergic neurons tested, and this effect disappeared after washout of the drug (Fig. 5a).

Perfusion of NAc slices with DA induced a reversible depolarization in most of the neurons tested without changing their input resistance.

Thus, NgR is not essential for mediating inhibitory signals from CNS myelin, at least in the neurons tested, whereas p75 NTR) plays a central role in this response.

Similary, upon perfusion with DA (30 60 μM), the majority of NAc neurons tested in the present study (18 out of 35 cells) exhibited a membrane depolarization, although a few neurons exhibited either a membrane hyperpolarization (one out of 35) or a hyperpolarization followed by a depolarization (four out of 35).