Learning and memory and navigation literatures emphasize interactions between multiple memory systems: a flexible, planning-based system and a rigid, cached-value system. This has profound implications for decision-making. Recent conceptualizations of flexi-ble decision-making employ prospection and projection arising from a network involving the hippocampus. Recent recordings from rodent hippocampus in decision-making situations have found transient forward-shifted representations. Evaluation of that prediction and subsequent action-selection likely occurs downstream (e.g. in orbitofrontal cortex, in ventral and dorsomedial striatum). Classically, striatum has been identified as a critical component of the less-flexible, incremental system. Current evidence, however, suggests that striatum is involved in both flexible and stimulusresponse decision-making, with dorsolateral striatum involved in stimulus-response strategies and ventral and dorsomedial striatum involved in goal-directed strategies.
IntroductionTheoretical perspectives on decision-making processes have traditionally treated decisionmaking from a single system perspective. Within many models of reinforcement learning, decision-making is viewed as learning a mapping of situations (world-states) s to actions a that maximizes reward by calculating the expected value E(V(s, a)) [1].In contrast, the learning and memory literature has emphasized the interaction of multiple memory systems [2][3][4]. In the memory literature, these differences are distinguished between declarative and procedural systems [3]. Declarative information is broadly accessible in a range of circumstances and based on a variety of retrieval cues [5] whereas procedural information is narrowly bound and accessible only in rigid and specific sequences [6]. In the navigation literature, these differences are distinguished between cognitive map and stimulus-response (route-based) systems [7, 8]. The cognitive map system confers animals with the ability to plan trajectories within their environment and flexibly integrate new information (such as novel stimuli and reward). Stimulus-response systems provide the basis for simpler, non-integrated navigation functions such as stimulus recognition and approach.Although many computational models of these systems have been presented, confirmation of specific mechanisms within the neurophysiology has been limited [8, 9]. Even without specific mechanisms, there has been a convergence in the proposed anatomical substrates underlying each component. These theories generally distinguish between a flexible planning system critically dependent on intact hippocampal function and a more rigid, more efficient system critically dependent on intact striatal function [3,4, 8, 10]. As we review © 2008 Elsevier Ltd. All rights reserved. Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copye...