The hippocampus is critical for spatial learning and memory. Hippocampal neurons in awake animals exhibit place field activity that encodes current location, as well as sharp-wave ripple (SWR) activity during which representations based on past experiences are often replayed. The relationship between these patterns of activity and the memory functions of the hippocampus is poorly understood. We interrupted awake SWRs in animals learning a spatial alternation task. We observed a specific learning and performance deficit that persisted throughout training. This deficit was associated with awake SWR activity, as SWR interruption left place field activity and post-experience SWR reactivation intact. These results provide a link between awake SWRs and hippocampal memory processes, which suggests that awake replay of memory-related information during SWRs supports learning and memory-guided decision-making.

Nucleus accumbens (NAc) inactivation increases food intake, indicating that NAc neurons exert ongoing inhibition of feeding. We previously described a subpopulation of NAc neurons that pause during sucrose licking and proposed that the pause permits consumption. We tested this hypothesis by first recording NAc neurons during sucrose consumption, and then electrically stimulating through the same electrodes. A large proportion of NAc shell and core neurons were inhibited during sucrose consumption, and local electrical stimulation abruptly interrupted licking. Effective stimulation sites were more anterior than ineffective sites in NAc. At low stimulus intensities, licking resumed immediately on stimulation offset. The latency to lick resumption from NAc neuron inhibition onset (ϳ460 ms) was very similar to that after electrical stimulation offset (ϳ440 ms). These results directly support the hypothesis that a significant subpopulation of NAc neurons inhibit palatable food consumption and that a pause in their firing is required to initiate and maintain consumption.

When rats and mice are free to explore a familiar environment they spend more time in a previously rewarded location. This conditioned place preference (CPP) results from an increased probability of initiating transitions from an unrewarded location to one previously paired with reward. We recorded nucleus accumbens (NAc) neurons while rats explored a three-room in-line apparatus. Before place conditioning, approximately equal proportions of NAc neurons show excitations or inhibitions when the rat is in each of the rooms (morphine paired, center or saline paired). Conditioning increased the proportion of neurons inhibited while the rat was in the morphine room and neurons excited in the saline room. Many of the neurons in these two groups responded during room transitions. Furthermore, the postconditioning increase in the population of neurons with room-selective responding persisted for several weeks after the last morphine treatment. This long-lasting change in population responses of NAc neurons to initially neutral locations is a neural correlate of the change in location preference manifest as CPP.

German PW, Fields HL. How prior reward experience biases exploratory movements: a probabilistic model. J Neurophysiol 97: 2083-2093, 2007. First published November 8, 2006 doi:10.1152/jn.00303.2006. Animals return to rewarded locations. An example of this is conditioned place preference (CPP), which is widely used in studies of drug reward. Although CPP is expressed as increased time spent in a previously rewarded location, the behavioral strategy underlying this change is unknown. We continuously monitored rats (n ϭ 22) in a three-room in-line configuration, before and after morphine conditioning in one end room. Although sequential room visit durations were variable, their probability distribution was exponential, indicating that the processes controlling visit durations can be modeled by instantaneous room exit probabilities. Further analysis of room transitions and computer simulations of probabilistic models revealed that the exploratory bias toward the morphine room is best explained by an increase in the probability of a subset of rapid, direct transitions from the saline-to the morphine-paired room by the central room. This finding sharply delineates and constrains possible neural mechanisms for a class of self-initiated, goal-directed behaviors toward previously rewarded locations.