In
the straight alley, a rat can be trained to approach a goal box in order
to obtain a liquidor food reward. The rat will usually be placed on
a food or water restricted schedule in order to motivate it to approach
the reward. The straight alley is divided into three main parts: 1)
The startbox, 2) the runway, and 3) the goalbox. The startbox is divided
from the runway by a sliding door. At the beginning of each session
the rat is placed in the startbox facing away from the sliding door;
once the rat has turned towards the door it is opened and three timers
are started. When the rat enters the runway a light beam connected to
one of the timers is broken. This gives a time measurement of the time
elapsed between the opening of the startbox door and the rats entrance
into the runway. Within the runway itself there are two small hurdles
that the rat must negotiate. Within the middle of the runway a second
light sensor measures the time it took the rat to reach the middle of
the runway since the opening of the startbox door. At the end of the
straight alley lies the goalbox. Within the goalbox rests a small cup
that usually contains the food reward (sugar or grain pellets). A light
beam between the runway and the goalbox is broken when the rat passes
by and gives a measurement of how long it took the rat to reach the
goalbox. A fourth measurement is often taken of how long it takes the
rat to consume its reward.
Various
behavioral manipulations can be employed with this procedure. Many studies
have found that when an animal is trained to expect a reward of a certain
kind or quantity, changing the magnitude of the reward (e.g. reducing
the amount) or changing the reward (e.g. replacing a banana with lettuce)
results in alterations in behavior. This effect has often been termed
learned frustration.
For example, when rats trained to approach the goal end of a straight
alley are shifted from a large reward (10 food pellets) to a smaller
reward (1 pellet) a significant decrease in running speed is observed.
An increase in reward magnitude (1 pellet to 10 pellets) will also produce
an increase in running speed.
The learning of this kind of shift has been found to be dependent upon
the integrity of the amygdala, hippocampus, and nucleus accumbens. Current
research in our lab examines hemispheric differences in amygdala norepinephrine
response to shifts in reward magnitude as well as the effects of lesions
and reversible inactivation of regions within the frontal cortex.