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Experiences of animal and human beings are structured by the continuity of space and time coupled with the uni-directionality of time. In addition to its pivotal position in spatial processing and navigation, the hippocampal system also plays a central, multiform role in several types of temporal processing. These include timing and sequence learning, at scales ranging from meso-scales of seconds to macro-scales of minutes, hours, days and beyond, encompassing the classical functions of short term memory, working memory, long term memory, and episodic memories (comprised of information about when, what, and where). This review article highlights the principal findings and behavioral contexts of experiments in rats showing: 1) timing: tracking time during delays by hippocampal 'time cells' and during free behavior by hippocampal-afferent lateral entorhinal cortex ramping cells; 2) 'online' sequence processing: activity coding sequences of events during active behavior; 3) 'off-line' sequence replay: during quiescence or sleep, orderly reactivation of neuronal assemblies coding awake sequences. Studies in humans show neurophysiological correlates of episodic memory comparable to awake replay. Neural mechanisms are discussed, including ion channel properties, plateau and ramping potentials, oscillations of excitation and inhibition of population activity, bursts of high amplitude discharges (sharp wave ripples), as well as short and long term synaptic modifications among and within cell assemblies. Specifically conceived neural network models will suggest processes supporting the emergence of scalar properties (Weber's law), and include different classes of feedforward and recurrent network models, with intrinsic hippocampal coding for 'transitions' (sequencing of events or places)., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

When facing a choice at a decision point in a maze, rats often display hesitations, pauses and reorientations. Such "vicarious trial and error" (VTE) behavior is thought to reflect decision making about which choice option is best, and thus a deliberation process. Although deliberation relies on a wide neural network, the dorsal hippocampus appears to play a prominent role through both its neural activity and its dynamic interplay with other brain areas. In contrast, the involvement of the ventral hippocampus in deliberation is unexplored. Here, we compared directly the effects of dorsal (dHPC) and ventral intermediate (vHPC) hippocampal inactivations induced by intracerebral muscimol injections on VTE behavior as a model of deliberation. To this aim, we analyzed VTE events as rats were required to switch strategy to a new unlearned reward rule. We used a protocol in which task performance in muscimol-injected animals was minimally altered so as to evidence specific effects on VTE behavior. Our results show subtle alterations in VTE behavior following dHPC, but not vHPC, inactivations, therefore suggesting a specific contribution of the dorsal hippocampus to deliberation through its role in prospective evaluation of future actions., Competing Interests: Declaration of Competing Interest The authors declare no competing financial interests, (Copyright © 2020 Elsevier B.V. All rights reserved.)

Hippocampal place cells show position-specific activity thought to reflect a self-localization signal. Several reports also point to some form of goal encoding by place cells. We investigated this by asking whether they also encode the value of spatial goals, which is crucial information for optimizing goal-directed navigation. We used a continuous place navigation task in which male rats navigate to one of two (freely chosen) unmarked locations and wait, triggering the release of reward, which is then located and consumed elsewhere. This allows sampling of place fields and dissociates spatial goal from reward consumption. The two goals varied in the amount of reward provided, allowing assessment of whether the rats factored goal value into their navigational choice and of possible neural correlates of this value. Rats successfully learned the task, indicating goal localization, and they preferred higher-value goals, indicating processing of goal value. Replicating previous findings, there was goal-related activity in the out-of-field firing of CA1 place cells, with a ramping-up of firing rate during the waiting period, but no general overrepresentation of goals by place fields, an observation that we extended to CA3 place cells. Importantly, place cells were not modulated by goal value. This suggests that dorsal hippocampal place cells encode space independently of its associated value despite the effect of that value on spatial behavior. Our findings are consistent with a model of place cells in which they provide a spontaneously constructed value-free spatial representation rather than encoding other navigationally relevant but nonspatial information. SIGNIFICANCE STATEMENT We investigated whether hippocampal place cells, which compute a self-localization signal, also encode the relative value of places, which is essential information for optimal navigation. When choosing between two spatial goals of different value, rats preferred the higher-value goal. We saw out-of-field goal firing in place cells, replicating previous observations that the cells are influenced by the goal, but their activity was not modulated by the value of these goals. Our results suggest that place cells do not encode all of the navigationally relevant aspects of a place, but instead form a value-free "map" that links to such aspects in other parts of the brain., (Copyright © 2019 Duvelle et al.)

The reuniens (Re) and rhomboid (Rh) nuclei of the ventral midline thalamus are reciprocally connected with the hippocampus (Hip) and the medial prefrontal cortex (mPFC). Growing evidence suggests that these nuclei might play a crucial role in cognitive processes requiring Hip-mPFC interactions, including spatial navigation. Here, we tested the effect of ReRh lesions on the firing properties and spatial activity of dorsal hippocampal CA1 place cells as male rats explored a familiar or a novel environment. We found no change in the spatial characteristics of CA1 place cells in the familiar environment following ReRh lesions. Contrariwise, spatial coherence was decreased during the first session in a novel environment. We then investigated field stability of place cells recorded across 5 d both in the familiar and in a novel environment presented in a predefined sequence. While the remapping capacity of the place cells was not affected by the lesion, our results clearly demonstrated a disruption of the CA1 cellular representation of both environments in ReRh rats. More specifically, we found ReRh lesions to produce (1) a pronounced and long-lasting decrease of place field stability and (2) a strong alteration of overdispersion (i.e., firing variability). Thus, in ReRh rats, exploration of a novel environment appears to interfere with the representation of the familiar one, leading to decreased field stability in both environments. The present study shows the involvement of ReRh nuclei in the long-term spatial stability of CA1 place fields. SIGNIFICANCE STATEMENT Growing evidence suggest that the ventral midline thalamic nuclei (reuniens and rhomboid) might play a substantial role in various cognitive tasks including spatial memory. In the present article, we show that the lesions of these nuclei impair the spatial representations encoded by CA1 place cells of both familiar and novel environments. First, reduced variability of place cell firing appears to indicate an impairment of attentional processes. Second, impaired stability of place cell representations could explain the long-term memory deficits observed in previous behavioral studies., (Copyright © 2018 the authors 0270-6474/18/380158-15$15.00/0.)

Recent interest in the neural bases of spatial navigation stems from the discovery of neuronal populations with strong, specific spatial signals. The regular firing field arrays of medial entorhinal grid cells suggest that they may provide place cells with distance information extracted from the animal's self-motion, a notion we critically review by citing new contrary evidence. Next, we question the idea that grid cells provide a rigid distance metric. We also discuss evidence that normal navigation is possible using only landmarks, without self-motion signals. We then propose a model that supposes that information flow in the navigational system changes between light and dark conditions. We assume that the true map-like representation is hippocampal and argue that grid cells have a crucial navigational role only in the dark. In this view, their activity in the light is predominantly shaped by landmarks rather than self-motion information, and so follows place cell activity; in the dark, their activity is determined by self-motion cues and controls place cell activity. A corollary is that place cell activity in the light depends on non-grid cells in ventral medial entorhinal cortex. We conclude that analysing navigational system changes between landmark and no-landmark conditions will reveal key functional properties.

Encoding of a goal with a specific value while performing a place navigation task involves the medial prefrontal cortex (mPFC) and the dorsal hippocampus (dHPC), and depends on the coordination between mPFC and the ventro-intermediate hippocampus (vHPC).The present work investigates the contribution of mPFC, dHPC, and vHPC when the rat has to update the value of a goal. Rats were trained to navigate to an uncued goal in order to release a food pellet in a continuous place navigation task. When they had reached criterion performance level in the task, they were subjected to a single "flash session" in which they were exposed to an aversive strobe light during goal visits instead of receiving a food reward. Just before the flash session, the GABA(A) agonist muscimol was injected to temporarily inactivate mPFC, dHPC, or vHPC. The ability to recall the changed value of the goal was tested on the next day. We first demonstrate the aversive effect of the strobe light by showing that rats learn to avoid the goal much more rapidly in the flash session than during a simple extinction session in which goal visits are not rewarded. Furthermore, while dHPC inactivation had no effect on learning and recalling the new goal value, vHPC muscimol injections considerably delayed goal value updating during the flash session, which resulted in a slight deficit during recall. In contrast, mPFC muscimol injections induced faster goal value updating but the rats were markedly impaired on recalling the new goal value on the next day. These results suggest that, contrary to mPFC and dHPC, vHPC is required for updating the value of a goal. In contrast, mPFC is necessary for long-term retention of this updating., (Copyright © 2013 Wiley Periodicals, Inc.)

Previous work shows that medial prefrontal cortex (mPFC) cells exhibit spatio-selective activity at a goal location when rats are trained in a goal-oriented navigation task. Damaging the ventral and intermediate hippocampal regions severely disrupts both mPFC goal firing and behavioral performance in the same task. Additionally, hippocampal place cells tend to develop a secondary place field at the goal location, suggesting that goal locations can be encoded by local changes in firing rate, within an otherwise stable spatial representation. Therefore, it has been suggested that the coordinated activity of a large fraction of hippocampal cells at the goal location may interact with the mPFC to compute accurate planning trajectories, relying on both precise location-specific firing of place cells and the coarse-coded, goal-trajectory planning function of the prefrontal cortex. To test this hypothesis, we inactivated the mPFC and recorded hippocampal place cell activity while animals were performing the navigation task. The results show that post-training inactivation of the prefrontal cortex does not affect behavioral performance, suggesting that this structure is no longer required when animals are overtrained. The goal-related activity of place cells was not affected at either single unit or local field potential level. Conversely, profound modifications of place cell firing variability (overdispersion) were observed after suppression of prefrontal input, suggesting a possible mechanism underlying behavioral flexibility.

Recent work on the neural substrate of spatial memory strongly suggests the existence of a neuronal network dedicated to the coding of spatial information and allowing the subject to orient in space. This network includes place cells of the hippocampus, head direction cells which are found in several brain regions and particularly the post-subiculum, and grid cells in the entorhinal cortex. Several recently discovered features of place cell activity shed light on how the hippocampus contributes to memory construction. For instance, learning a novel environment relies on a dynamic population code in which place cell activity suddenly changes towards stable states built during previous experience. We briefly review these properties to show how they constrain the hippocampal memory code., (© Société de Biologie, 2010.)

Zif268 is a transcriptional regulator that plays a crucial role in maintenance of the late phases of hippocampal long-term potentiation (LTP) and consolidation of spatial memories. Because the hippocampal place cell system is essential for long-term spatial memory, we tested the hypothesis that zif268 is required for long-term stability of hippocampal place cell representations by recording CA1 place cells in mice lacking zif268. We found that zif268 gene deletion destabilized the representation of a familiar environment after exposure to a novel environment and impaired the long-term (24 h), but not short-term (1 h), stability of newly formed representations. These impairments could be rescued by repeated exposure to the novel environment, however. These results indicate that zif268 contributes to the long-term stability of spatial representations in CA1 and support the notion that the long-term stability of place cell representations requires transcription-dependent mechanisms similar to those observed in LTP.

The medial prefrontal cortex (mPFC) of the rat receives a prominent input from the ventral two thirds of the hippocampus, a structure important for spatial awareness, working memory and motivation. We recently found [Hok V, Lenck-Santini PP, Roux S, Save E, Muller RU, Poucet B. Goal-related activity in hippocampal place cells. J Neurosci 2007;27:472-82.] that neurones in the dorsal hippocampus exhibit anticipatory firing prior to the release of a food pellet on an operant task. Here we look for similar activity in the mPFC on the same task and test whether this activity is dependent on the hippocampus. Rats were trained to navigate to a goal zone, wait for the release of a food pellet and then forage for the pellet while unit activity was recorded in the prelimbic and infralimbic areas of the mPFC. Two 16 min sessions were conducted per day, one session with the goal delimited by a cue disc, the second without the cue. In controls, a large proportion of mPFC neurones exhibited activity similar to that seen in the hippocampus while the animal was stationary at the goal. Over half exhibited the same activity regardless of goal location. Anticipatory activity was largely abolished in animals with bilateral lesions of the ventral and intermediate hippocampus, both in cued and uncued sessions. Even though lesioned animals continued to perform the task, they tended to leave the goal zone prematurely. We suggest that the anticipatory activity in the mPFC is dependent on similar activity in the hippocampus and that both structures have a role in either impulse control or reward expectation.

Place cells are hippocampal neurons whose discharge is strongly related to a rat's location in its environment. The existence of place cells has led to the proposal that they are part of an integrated neural system dedicated to spatial navigation. To further understand the relationships between place cell firing and spatial problem solving, we examined the discharge of CA1 and CA3 place cells as rats were exposed to a shortcut in a runway maze. On specific sessions, a wall section of the maze was removed so as to open a shorter novel route within the otherwise familiar maze. We found that the discharge of both CA1 and CA3 cells was strongly affected in the vicinity of the shortcut region but was much less affected farther away. In addition, CA3 fields away from the shortcut were more altered than CA1 fields. Thus, place cell firing appears to reflect more than just the animal's spatial location and may provide additional information about possible motions, or routes, within the environment. This kinematic representation appears to be spatially more extended in CA3 than in CA1, suggesting interesting computational differences between the two subregions.

Recent studies emphasize the importance of the entorhinal cortex in spatial representation and navigation. Furthermore, evidence is accumulating to show that spatial processing depends on interactions between the entorhinal cortex and the hippocampus. To investigate these interactions, we examined the effects of entorhinal cortex lesions on the activity of hippocampal CA1 place cells. Rats received bilateral radiofrequency lesions of the entorhinal cortex or sham lesions before place cell recording. Place cells were recorded as the rats performed a pellet-chasing task in a cylinder containing three cue-objects. Entorhinal cortex lesions did not abolish place cell spatial firing but reduced noticeably discharge rate and field size. Most importantly, the lesions affected firing field stability when cells were recorded both in constant conditions and following cue manipulations (object rotation, object removal). These findings indicate that the entorhinal cortex is necessary for the stability of hippocampal representations across exposures to a familiar environment. Consistent with the recent discovery of grid cells in the medial entorhinal cortex, our results suggest that the entorhinal cortex contributes to providing a spatial framework that would enable the hippocampus to maintain stable environment-specific representations.

Place cells are hippocampal neurons whose discharge is strongly related to a rat's location in its environment. The existence of place cells has led to the proposal that they are part of an integrated neural system dedicated to spatial navigation, an idea supported by the discovery of strong relationships between place cell activity and spatial problem solving. To further understand such relationships, we examined the discharge of place cells recorded while rats solved a place navigation task. We report that, in addition to having widely distributed firing fields, place cells also discharge selectively while the hungry rat waits in an unmarked goal location to release a food pellet. Such firing is not duplicated in other locations outside the main firing field even when the rat's behavior is constrained to be extremely similar to the behavior at the goal. We therefore propose that place cells provide both a geometric representation of the current environment and a reflection of the rat's expectancy that it is located correctly at the goal. This on-line feedback about a critical aspect of navigational performance is proposed to be signaled by the synchronous activity of the large fraction of place cells active at the goal. In combination with other (prefrontal) cells that provide coarse encoding of goal location, hippocampal place cells may therefore participate in a neural network allowing the rat to plan accurate trajectories in space.

The purpose of the present experiment was to examine how distal cues and proximal objects interact to control firing fields. In a previous study, Shapiro et al. (1997) Hippocampus 7:624-642, suggested that hippocampal place cell firing is controlled by distal cues and proximal floor inserts in a flexible and hierarchical fashion. Control exerted by the combined set of cues prevailed over control by distal cues, which itself prevailed over control by proximal cues. Here, we examined the generality of this hierarchy in the use of cues. Place cells were recorded as rats performed a pellet chasing task on a platform containing three proximal objects, surrounded by a curtain where three visual stimuli were hung. A double rotation of distal and proximal cue sets producing a 180 degrees mismatch revealed noncoherent responses of place cells. Most fields were controlled by the configuration of proximal and distal cues (i.e., remapped). Less often, fields were controlled by specific cues with a majority being controlled by proximal cues, thus suggesting that response hierarchy is modulated by the environment. We finally examined the effect of removing one set of cues after the double rotation session. Half of the fields were controlled by the remaining cues while the other half remapped, thus suggesting a competition between pattern completion and pattern separation processes. Furthermore, cells that were controlled by the remaining cues were mainly those that had remapped in the double rotation session. Our results are compatible with the idea that the flexibility of the place cell system results from an interaction between the sensory properties of individual cell and the attractor networks properties of the whole place cell population.

It has been recently shown that lesions of parahippocampal areas including the entorhinal cortex do not disrupt place learning in the water maze, suggesting that the hippocampo-cortical circuitry is not important for spatial memory [Burwell RD, Saddoris MP, Bucci DJ, Wiig KA. Corticohippocampal contributions to spatial and contextual learning. J Neurosci 2004;24:3826-36]. The aim of the present study was to tax more directly the cooperation between the hippocampus and entorhinal cortex in two different spatial tasks, a place navigation task and a spontaneous object exploration task, using a disconnection procedure. Damaging the entorhinal-hippocampal system induced impairments in the two tasks but only in the spatial object exploration task rats with contralateral lesions displayed a greater deficit than rats with ipsilateral lesions. The results suggest that the cooperation between the hippocampus and the entorhinal cortex is modulated by the nature of the task and the cognitive processes involved in formation of spatial memory.

The hippocampus and associative parietal cortex (APC) both contribute to spatial memory but the nature of their functional interaction remains unknown. To address this issue, we investigated the effects of APC lesions on hippocampal place cell firing in freely moving rats. Place cells were recorded from APC-lesioned and control rats as they performed a pellet-chasing task in a circular arena containing three object cues. During successive recording sessions, cue manipulations including object rotation in the absence of the rat and object removal in the presence of the rat were made to examine the control exerted by the objects or by non-visual intramaze cues on place field location, respectively. Object rotations resulted in equivalent field rotation for all cells in control rats. In contrast, a fraction of place fields in APC-lesioned rats did not rotate but remained stable relative to the room. Object removal produced different effects in APC-lesioned and control rats. In control rats, most place fields remained stable relative to the previous object rotation session, indicating that they were anchored to olfactory and/or idiothetic cues. In APC-lesioned rats, a majority of place fields shifted back to their initial, standard location, thus suggesting that they relied on uncontrolled background cues to maintain place field stability. These results provide strong evidence that the hippocampus and the APC cooperate in the formation of spatial memory and suggest that the APC is involved in elaboration of a hippocampal map based on proximal landmarks.

Humans can recognize and navigate in a room when its contents have been rearranged. Rats also adapt rapidly to movements of objects in a familiar environment. We therefore set out to investigate the neural machinery that underlies this capacity by further investigating the place cell-based map of the surroundings found in the rat hippocampus. We recorded from single CA1 pyramidal cells as rats foraged for food in a cylindrical arena (the room) containing a tall barrier (the furniture). Our main finding is a new class of cells that signal proximity to the barrier. If the barrier is fixed in position, these cells appear to be ordinary place cells. When, however, the barrier is moved, their activity moves equally and thereby conveys information about the barrier's position relative to the arena. When the barrier is removed, such cells stop firing, further suggesting they represent the barrier. Finally, if the barrier is put into a different arena where place cell activity is changed beyond recognition ("remapping"), these cells continue to discharge at the barrier. We also saw, in addition to barrier cells and place cells, a small number of cells whose activity seemed to require the barrier to be in a specific place in the environment. We conclude that barrier cells represent the location of the barrier in an environment-specific, place cell framework. The combined place + barrier cell activity thus mimics the current arrangement of the environment in an unexpectedly realistic fashion.

Hippocampal place cells are characterized by location-specific firing, that is each cell fires in a restricted region of the environment explored by the rat. In this review, we briefly examine the sensory information used by place cells to anchor their firing fields in space and show that, among the various sensory cues that can influence place cell activity, visual and motion-related cues are the most relevant. We then explore the contribution of several cortical areas to the generation of the place cell signal with an emphasis on the role of the visual cortex and parietal cortex. Finally, we address the functional significance of place cell activity and demonstrate the existence of a clear relationship between place cell positional activity and spatial navigation performance. We conclude that place cells, together with head direction cells, provide information useful for spatially guided movements, and thus provide a unique model of how spatial information is encoded in the brain.

This study examined the performance of spatial problems by rats when purely behavioral manipulations disturb the relationship between the place cell representation and the cues used to solve the problems. Place cells were recorded while rats performed a task in which they had to locate a goal in a gray cylinder. In the "far" task, the unmarked goal was displaced by a large fixed distance from a white card on the cylinder wall. In the "near" task, the unmarked goal was directly in front of the card. Finally, in the "cue" task the goal was marked by a black disk on the cylinder floor. Relationships between visible stimuli and place cell activity were manipulated by conducting either "hidden" (with the rat in its home cage) or "visible" (with the rat in the recording apparatus) rotations of the wall card and, when present, independent rotations of the black disk. Hidden card rotations generally caused equal firing field rotations, whereas visible card rotations often did not cause fields to move. In the far task, visible card rotations were associated with a strong decrease of correct responses in the card-referred goal area. Most rats tended to search the goal in the field-referred area. In the near task, visible card rotations were associated with a moderate decrease of performance, with rats searching the goal at the wall card. Finally, field placements had no effect on performance in the cue task. Thus, visible rotations tended to disrupt the relationship between firing fields and cues in all tasks but impaired performance only in the task that required map-based navigation. These results provide strong new evidence in favor of the spatial mapping theory of hippocampal function.

Place recognition is a complex process involving idiothetic and allothetic information. In mammals, evidence suggests that visual information stemming from the temporal and parietal cortical areas ('what' and 'where' information) is merged at the level of the entorhinal cortex (EC) to build a compact code of a place. Local views extracted from specific feature points can provide information important for view cells (in primates) and place cells (in rodents) even when the environment changes dramatically. Robotics experiments using conjunctive cells merging 'what' and 'where' information related to different local views show their important role for obtaining place cells with strong generalization capabilities. This convergence of information may also explain the formation of grid cells in the medial EC if we suppose that: (1) path integration information is computed outside the EC, (2) this information is compressed at the level of the EC owing to projection (which follows a modulo principle) of cortical activities associated with discretized vector fields representing angles and/or path integration, and (3) conjunctive cells merge the projections of different modalities to build grid cell activities. Applying modulo projection to visual information allows an interesting compression of information and could explain more recent results on grid cells related to visual exploration. In conclusion, the EC could be dedicated to the build-up of a robust yet compact code of cortical activity whereas the hippocampus proper recognizes these complex codes and learns to predict the transition from one state to another. [ABSTRACT FROM AUTHOR]

Since the discovery of place cells, the hippocampus is thought to be the neural substrate of a cognitive map. The later discovery of head direction cells, grid cells and border cells, as well as of cells with more complex spatial signals, has led to the idea that there is a brain system devoted to providing the animal with the information required to achieve efficient navigation. Current questioning is focused on how these signals are integrated in the brain. In this review, we focus on the issue of how self-localization is performed in the hippocampal place cell map. To do so, we first shortly review the sensory information used by place cells and then explain how this sensory information can lead to two coding modes, respectively based on external landmarks (allothetic information) and self-motion cues (idiothetic information). We hypothesize that these two modes can be used concomitantly with the rat shifting from one mode to the other during its spatial displacements. We then speculate that sequential reactivation of place cells could participate in the resetting of self-localization under specific circumstances and in learning a new environment. Finally, we provide some predictions aimed at testing specific aspects of the proposed ideas. [ABSTRACT FROM AUTHOR]

The existence of place cells, whose discharge is strongly related to a rat's location in its environment, has led to the proposal that they form part of an integrated neural system dedicated to spatial navigation. It has been suggested that this system could represent space as a cognitive map, which is flexibly used by animals to plan new shortcuts or efficient detours. To further understand the relationships between hippocampal place cell firing and cognitive maps, we examined the discharge of place cells as rats were exposed to a Tolman-type detour problem. In specific sessions, a transparent barrier was placed onto the maze so as to block the shortest central path between the two rewarded end locations of a familiar three-way maze. We found that rats rapidly and consistently chose the shortest alternative detour. Furthermore, both CA1 and CA3 place cells that had a field in the vicinity of the barrier displayed local remapping. In contrast, neither CA1 nor CA3 cells that had a field away from the barrier were affected. This finding, at odds with our previous report of altered CA3 discharge for distant fields in a shortcut task, suggests that the availability of a novel path and the blocking of a familiar path are not equivalent and could lead to different responses of the CA3 place cell population. Together, the two studies point to a specific role of CA3 in the representation of spatial connectivity and sequences. [ABSTRACT FROM AUTHOR]

Abstract: The processing of spatial information in the brain requires a network of structures within which the hippocampus plays a prominent role by elaborating an allocentric representation of space. The parietal cortex has long been suggested to have a complementary function. An overview of lesion and unit recording data in the rat indicates that the parietal cortex is involved in different aspects of spatial information processing including allocentric and egocentric processing. More specifically, the data suggest that the parietal cortex plays a fundamental role in combining visual and motion information, a process that would be important for an egocentric-to-allocentric transformation process. Furthermore, the parietal cortex may also have a role in the long-term storage of representation although this possibility needs further evidence. The data overall show that the parietal cortex occupies a unique position in the brain at the interface of perception and representation. [Copyright &y& Elsevier]

Place cells are hippocampal pyramidal neurons that discharge strongly in relation to the rat's location in the environment. We recently reported that many place cells recorded from rats performing place or cue navigation tasks also discharged when they were at the goal location rather than in the primary firing field. Furthermore, subtle differences in discharge timing were found in the two navigation tasks, with activity occurring later in the place task compared to the cue task. Here we tested the possibility that such delayed firing in the place task may reflect the differential involvement of time estimation, which would allow the rat to predict forthcoming reward delivery. More specifically, we reasoned that failure to obtain a reward after a fixed 2s delay in the place task reliably reflected the rat's misplacement relative to the correct location, thus making time a valuable cue to help the rat perform the task. To test this hypothesis, well-trained rats were run on a partial extinction procedure in place and cue navigation tasks so that no feed-back signal was provided about their actual accuracy during extinction periods. Although the time estimation hypothesis predicts that only in the place task will the rat make correction movements at the end of goal periods during extinction, we found that such movements occurred in all rats, indicating correct time estimation in both place and cue tasks. We briefly discuss the results in the light of current computational theories of hippocampal function. [ABSTRACT FROM AUTHOR]

Abstract Hippocampal place cells were recorded while rats with lesions of the striate visual cortex foraged for food pellets in a cylindrical arena. Compared to control rats, rats with striate damage had place cells whose firing was less well organized in space, according to a measurement of spatial coherence. More importantly, the spatial location of firing fields in rats with striate lesions was poorly controlled by three-dimensional objects, unlike the fields of either normal sighted rats or early blind rats. These findings suggest a possible contribution of the striate visual cortex to the selection of cues used for anchoring place cell firing fields in space. [ABSTRACT FROM AUTHOR]

Abstract Hippocampal place cells were recorded while rats solved a continuous spatial alternation task requiring short-term spatial memory. All cells that had a firing field on the stem of the Y-shaped maze were found to have a very similar pattern of discharge whether the rat was about to make a right or a left turn, and whether the preceding turn was a right or a left turn. Thus, the view that place cells encode a variety of events (including the direction of turns) useful for solving memory tasks is not well supported by the present data. We suggest several possible explanations to account for the discrepancy with other recent studies showing turn-related modulation of place-cell activity. [ABSTRACT FROM AUTHOR]