scholarly journals Sharp wave-associated activity patterns of olfactory cortical neurons in the mouse piriform cortex

2018 ◽  
Author(s):  
Kazuki Katori ◽  
Hiroyuki Manabe ◽  
Ai Nakashima ◽  
Eer Dunfu ◽  
Takuya Sasaki ◽  
...  
Keyword(s):  
Cortical Neurons ◽  
Slow Wave Sleep ◽  
Activity Patterns ◽  
Piriform Cortex ◽  
Associative Memories ◽  
Firing Rates ◽  
Anterior Piriform Cortex ◽  
Sharp Wave ◽  
Sharp Waves ◽  
Neural Activities

ABSTRACTThe olfactory piriform cortex is thought to participate in olfactory associative memory. Like the hippocampus, which is essential for episodic memory, it belongs to an evolutionally conserved paleocortex and comprises a three-layered cortical structure. During slow-wave sleep, the olfactory piriform cortex becomes less responsive to external odor stimuli and instead displays sharp wave (SPW) activity similar to that observed in the hippocampus. Neural activity patterns during hippocampal SPW have been intensively studied in terms of memory consolidation; however, little is known about the activity patterns of olfactory cortical neurons during olfactory cortex sharp waves (OC-SPWs). In this study, we recorded multi-unit neural activities in the anterior piriform cortex in urethane-anesthetized mice. We found that the activity patterns of olfactory cortical neurons during OC-SPWs were non-randomly organized. Individual olfactory cortical neurons varied in the timings of their peak firing rates during OC-SPW events. Moreover, specific pairs of olfactory cortical neurons were more frequently activated together than expected by chance. On the basis of these observations, we speculate that coordinated activation of specific subsets of olfactory cortical neurons repeats during OC-SPWs, thereby facilitating synaptic plasticity underlying the consolidation of olfactory associative memories.

scholarly journals Sharp wave-associated synchronized inputs from the piriform cortex activate olfactory tubercle neurons during slow-wave sleep

2014 ◽  
Vol 111 (1) ◽  
pp. 72-81 ◽  
Author(s):  
Kimiya Narikiyo ◽  
Hiroyuki Manabe ◽  
Kensaku Mori
Keyword(s):  
Slow Wave ◽  
Olfactory System ◽  
Slow Wave Sleep ◽  
Piriform Cortex ◽  
Current Source ◽  
Olfactory Tubercle ◽  
Neuronal Circuitry ◽  
Anterior Piriform Cortex ◽  
Sharp Waves ◽  
Density Analysis

During slow-wave sleep, anterior piriform cortex neurons show highly synchronized discharges that accompany olfactory cortex sharp waves (OC-SPWs). The OC-SPW-related synchronized activity of anterior piriform cortex neurons travel down to the olfactory bulb and is thought to be involved in the reorganization of bulbar neuronal circuitry. However, influences of the OC-SPW-related activity on other regions of the central olfactory system are still unknown. Olfactory tubercle is an area of OC and part of ventral striatum that plays a key role in reward-directed motivational behaviors. In this study, we show that in freely behaving rats, olfactory tubercle receives OC-SPW-associated synchronized inputs during slow-wave sleep. Local field potentials in the olfactory tubercle showed SPW-like activities that were in synchrony with OC-SPWs. Single-unit recordings showed that a subpopulation of olfactory tubercle neurons discharged in synchrony with OC-SPWs. Furthermore, correlation analysis of spike activity of anterior piriform cortex and olfactory tubercle neurons revealed that the discharges of anterior piriform cortex neurons tended to precede those of olfactory tubercle neurons. Current source density analysis in urethane-anesthetized rats indicated that the current sink of the OC-SPW-associated input was located in layer III of the olfactory tubercle. These results indicate that OC-SPW-associated synchronized discharges of piriform cortex neurons travel to the deep layer of the olfactory tubercle and drive discharges of olfactory tubercle neurons. The entrainment of olfactory tubercle neurons in the OC-SPWs suggests that OC-SPWs coordinate reorganization of neuronal circuitry across wide areas of the central olfactory system including olfactory tubercle during slow-wave sleep.

scholarly journals Sharp wave‐associated activity patterns of cortical neurons in the mouse piriform cortex

2018 ◽  
Vol 48 (10) ◽  
pp. 3246-3254
Author(s):  
Kazuki Katori ◽  
Hiroyuki Manabe ◽  
Ai Nakashima ◽  
Eer Dunfu ◽  
Takuya Sasaki ◽  
...  
Keyword(s):  
Cortical Neurons ◽  
Activity Patterns ◽  
Piriform Cortex ◽  
Sharp Wave

scholarly journals An In Vitro Model of Hippocampal Sharp Waves: Regional Initiation and Intracellular Correlates

2005 ◽  
Vol 94 (1) ◽  
pp. 741-753 ◽  
Author(s):  
Chiping Wu ◽  
Marjan Nassiri Asl ◽  
Jesse Gillis ◽  
Frances K. Skinner ◽  
Liang Zhang
Keyword(s):  
Dentate Gyrus ◽  
Large Amplitude ◽  
Pyramidal Neurons ◽  
Slow Wave Sleep ◽  
Hippocampal Slices ◽  
Field Potentials ◽  
Sharp Wave ◽  
Sharp Waves ◽  
Hippocampal Circuitry

During slow wave sleep and consummatory behaviors, electroencephalographic recordings from the rodent hippocampus reveal large amplitude potentials called sharp waves. The sharp waves originate from the CA3 circuitry and their generation is correlated with coherent discharges of CA3 pyramidal neurons and dependent on activities mediated by AMPA glutamate receptors. To model sharp waves in a relatively large hippocampal circuitry in vitro, we developed thick (1 mm) mouse hippocampal slices by separating the dentate gyrus from the CA2/CA1 areas while keeping the functional dentate gyrus-CA3-CA1 connections. We found that large amplitude (0.3–3 mV) sharp wave-like field potentials occurred spontaneously in the thick slices without extra ionic or pharmacological manipulation and they resemble closely electroencephalographic sharp waves with respect to waveform, regional initiation, pharmacological manipulations, and intracellular correlates. Through measuring tissue O2, K+, and synaptic and single cell activities, we verified that the sharp wave-like potentials are not a consequence of anoxia, nonspecific elevation of extracellular K+ and dissection-related tissue damage. Our data suggest that a subtle but crucial increase in the CA3 glutamatergic activity effectively recruits a population of neurons thus responsible for the generation of the sharp wave-like spontaneous field potentials in isolated hippocampal circuitry.

scholarly journals Temporal coordination of olfactory cortex sharp-wave activity with up- and downstates in the orbitofrontal cortex during slow-wave sleep

2017 ◽  
Vol 117 (1) ◽  
pp. 123-135 ◽  
Author(s):  
Naomi Onisawa ◽  
Hiroyuki Manabe ◽  
Kensaku Mori
Keyword(s):  
Slow Wave ◽  
Orbitofrontal Cortex ◽  
Slow Wave Sleep ◽  
Time Windows ◽  
Late Phase ◽  
Piriform Cortex ◽  
Olfactory Cortex ◽  
Field Potentials ◽  
Temporal Coordination ◽  
Anterior Piriform Cortex

During slow-wave sleep, interareal communications via coordinated, slow oscillatory activities occur in the large-scale networks of the mammalian neocortex. Because olfactory cortex (OC) areas, which belong to paleocortex, show characteristic sharp-wave (SPW) activity during slow-wave sleep, we examined whether OC SPWs in freely behaving rats occur in temporal coordination with up- and downstates of the orbitofrontal cortex (OFC) slow oscillation. Simultaneous recordings of local field potentials and spike activities in the OC and OFC showed that during the downstate in the OFC, the OC also exhibited downstate with greatly reduced neuronal activity and suppression of SPW generation. OC SPWs occurred during two distinct phases of the upstate of the OFC: early-phase SPWs occurred at the start of upstate shortly after the down-to-up transition in the OFC, whereas late-phase SPWs were generated at the end of upstate shortly before the up-to-down transition. Such temporal coordination between neocortical up- and downstates and olfactory system SPWs was observed between the prefrontal cortex areas (OFC and medial prefrontal cortex) and the OC areas (anterior piriform cortex and posterior piriform cortex). These results suggest that during slow-wave sleep, OC and OFC areas communicate preferentially in specific time windows shortly after the down-to-up transition and shortly before the up-to-down transition. NEW & NOTEWORTHY Simultaneous recordings of local field potentials and spike activities in the anterior piriform cortex (APC) and orbitofrontal cortex (OFC) during slow-wave sleep showed that APC sharp waves tended to occur during two distinct phases of OFC upstate: early phase, shortly after the down-to-up transition, and late phase, shortly before the up-to-down transition, suggesting that during slow-wave sleep, olfactory cortex and OFC areas communicate preferentially in the specific time windows.

Low-Probability Transmission of Neocortical and Entorhinal Impulses Through the Perirhinal Cortex

2004 ◽  
Vol 91 (5) ◽  
pp. 2079-2089 ◽  
Author(s):  
Joe Guillaume Pelletier ◽  
John Apergis ◽  
Denis Paré
Keyword(s):  
Hippocampal Neurons ◽  
Slow Wave Sleep ◽  
Time Window ◽  
Activity Patterns ◽  
Perirhinal Cortex ◽  
Sharp Waves ◽  
Low Probability ◽  
Unanesthetized Animals ◽  
Artificial Nature ◽  
Electrical Stimuli

One model of episodic memory posits that during slow-wave sleep (SWS), the synchronized discharges of hippocampal neurons in relation to sharp waves “replay” activity patterns that occurred during the waking state, facilitating synaptic plasticity in the neocortex. Although evidence of replay was found in the hippocampus in relation to sharp waves, it was never shown that this activity reached the neocortex. Instead, it was assumed that the rhinal cortices faithfully transmit information from the hippocampus to the neocortex and reciprocally. Here, we tested this idea using 3 different approaches. 1) Stimulating electrodes were inserted in the entorhinal cortex and temporal neocortex and evoked unit responses were recorded in between them, in the intervening rhinal cortices. In these conditions, impulse transfer occurred with an extremely low probability, in both directions. 2) To rule out the possibility that this unreliable transmission resulted from the artificial nature of electrical stimuli, crosscorrelation analyses of spontaneous neocortical, perirhinal, and entorhinal firing were performed in unanesthetized animals during the states of waking and SWS. Again, little evidence of propagation could be obtained in either state. 3) To test the idea that propagation occurs only when large groups of neurons are activated within a narrow time window, we computed perievent histograms of neocortical, perirhinal, and entorhinal neuronal discharges around large-amplitude sharp waves. However, these synchronized entorhinal discharges also failed to propagate across the perirhinal cortex. These findings suggest that the rhinal cortices are more than a relay between the neocortex and hippocampus, but rather a gate whose properties remain to be identified.

Natural Waking and Sleep States: A View From Inside Neocortical Neurons

2001 ◽  
Vol 85 (5) ◽  
pp. 1969-1985 ◽  
Author(s):  
M. Steriade ◽  
I. Timofeev ◽  
F. Grenier
Keyword(s):  
Slow Wave ◽  
Cortical Neurons ◽  
Slow Wave Sleep ◽  
Input Resistance ◽  
Spiking Neurons ◽  
Firing Patterns ◽  
Firing Rates ◽  
Waking And Sleep ◽  
Neocortical Neurons ◽  
Fast Spiking

In this first intracellular study of neocortical activities during waking and sleep states, we hypothesized that synaptic activities during natural states of vigilance have a decisive impact on the observed electrophysiological properties of neurons that were previously studied under anesthesia or in brain slices. We investigated the incidence of different firing patterns in neocortical neurons of awake cats, the relation between membrane potential fluctuations and firing rates, and the input resistance during all states of vigilance. In awake animals, the neurons displaying fast-spiking firing patterns were more numerous, whereas the incidence of neurons with intrinsically bursting patterns was much lower than in our previous experiments conducted on the intact-cortex or isolated cortical slabs of anesthetized cats. Although cortical neurons displayed prolonged hyperpolarizing phases during slow-wave sleep, the firing rates during the depolarizing phases of the slow sleep oscillation was as high during these epochs as during waking and rapid-eye-movement sleep. Maximum firing rates, exceeding those of regular-spiking neurons, were reached by conventional fast-spiking neurons during both waking and sleep states, and by fast-rhythmic-bursting neurons during waking. The input resistance was more stable and it increased during quiet wakefulness, compared with sleep states. As waking is associated with high synaptic activity, we explain this result by a higher release of activating neuromodulators, which produce an increase in the input resistance of cortical neurons. In view of the high firing rates in the functionally disconnected state of slow-wave sleep, we suggest that neocortical neurons are engaged in processing internally generated signals.

scholarly journals Increased pattern similarity in two major olfactory cortices despite higher sparseness levels

2021 ◽  
Author(s):  
Chaviva Markind ◽  
Prosenjit Kundu ◽  
Mor Barak ◽  
Rafi Haddad
Keyword(s):  
Activity Patterns ◽  
Piriform Cortex ◽  
List Type ◽  
Activity Levels ◽  
Anterior Piriform Cortex ◽  
Odor Processing ◽  
Pattern Similarity ◽  
Fundamental Process ◽  
Cortical Regions ◽  
Odor Representation

AbstractPattern separation is a fundamental process that enhances discrimination of similar stimuli and can be achieved by sparsening the neural activity and expanding the coding space. Odor stimuli evoke patterns of activity in the olfactory bulb (OB) and these activity patterns are projected to several cortical regions that contain larger numbers of neurons and show sparser activity levels. However, whether these projected patterns are better separated is still unclear. Here we compared odor responses in the OB, anterior piriform cortex (aPC) and anterior olfactory nucleus (AON) to the exact same odor stimuli. We found that odor representations are more similar, noisier and less distinctive in aPC and AON than in the OB. The increase in similarity was observed for both similar and dissimilar odors. Modeling odor transformation from the OB to the olfactory cortex using simulated as well as actual OB odor responses as inputs, demonstrates that the observed rise in odor representation similarity can be explained by assuming biologically plausible variation in the number of OB inputs each cortical neuron receives. We discuss the possible advantages of our findings to odor processing in the aPC and AON.HighlightsOdor representations in the aPC and AON are more correlated despite increase in sparseness levels.Odor identity is best represented in the OB.Variance in the number of inputs from OB can explain the reduction in odor separation.

scholarly journals Intra- and interregional cortical interactions related to sharp-wave ripples and dentate spikes

2017 ◽  
Vol 117 (2) ◽  
pp. 556-565 ◽  
Author(s):  
Drew B. Headley ◽  
Vasiliki Kanta ◽  
Denis Paré
Keyword(s):  
Memory Consolidation ◽  
Cortical Neurons ◽  
Slow Wave Sleep ◽  
Dorsal Hippocampus ◽  
Gamma Oscillations ◽  
Sharp Wave ◽  
Up States ◽  
Gamma Coherence ◽  
Cortical Regions ◽  
The Relationship

The hippocampus generates population events termed sharp-wave ripples (SWRs) and dentate spikes (DSs). While little is known about DSs, SWR-related hippocampal discharges during sleep are thought to replay prior waking activity, reactivating the cortical networks that encoded the initial experience. During slow-wave sleep, such reactivations likely occur during up-states, when most cortical neurons are depolarized. However, most studies have examined the relationship between SWRs and up-states measured in single neocortical regions. As a result, it is currently unclear whether SWRs are associated with particular patterns of widely distributed cortical activity. Additionally, no such investigation has been carried out for DSs. The present study addressed these questions by recording SWRs and DSs from the dorsal hippocampus simultaneously with prefrontal, sensory (visual and auditory), perirhinal, and entorhinal cortices in naturally sleeping rats. We found that SWRs and DSs were associated with up-states in all cortical regions. Up-states coinciding with DSs and SWRs exhibited increased unit activity, power in the gamma band, and intraregional gamma coherence. Unexpectedly, interregional gamma coherence rose much more strongly in relation to DSs than to SWRs. Whereas the increase in gamma coherence was time locked to DSs, that seen in relation to SWRs was not. These observations suggest that SWRs are related to the strength of up-state activation within individual regions throughout the neocortex but not so much to gamma coherence between different regions. Perhaps more importantly, DSs coincided with stronger periods of interregional gamma coherence, suggesting that they play a more important role than previously assumed. NEW & NOTEWORTHY Off-line cortico-hippocampal interactions are thought to support memory consolidation. We surveyed the relationship between hippocampal sharp-wave ripples (SWRs) and dentate spikes (DSs) with up-states across multiple cortical regions. SWRs and DSs were associated with increased cortical gamma oscillations. Interregional gamma coherence rose much more strongly in relation to DSs than to SWRs. Moreover, it was time locked to DSs but not SWRs. These results have important implications for current theories of systems memory consolidation during sleep.

scholarly journals Relationship between individual neuron and network spontaneous activity in developing mouse cortex

2014 ◽  
Vol 112 (12) ◽  
pp. 3033-3045 ◽  
Author(s):  
Heather M. Barnett ◽  
Julijana Gjorgjieva ◽  
Keiko Weir ◽  
Cara Comfort ◽  
Adrienne L. Fairhall ◽  
...  
Keyword(s):  
Normal Development ◽  
Activity Patterns ◽  
Piriform Cortex ◽  
Intrinsic Excitability ◽  
Intrinsic Activity ◽  
Dorsal Cortex ◽  
Synchronous Activity ◽  
Mouse Cortex ◽  
Propagating Waves ◽  
Autonomous Activity

Spontaneous synchronous activity (SSA) that propagates as electrical waves is found in numerous central nervous system structures and is critical for normal development, but the mechanisms of generation of such activity are not clear. In previous work, we showed that the ventrolateral piriform cortex is uniquely able to initiate SSA in contrast to the dorsal neocortex, which participates in, but does not initiate, SSA (Lischalk JW, Easton CR, Moody WJ. Dev Neurobiol 69: 407–414, 2009). In this study, we used Ca2+ imaging of cultured embryonic day 18 to postnatal day 2 coronal slices (embryonic day 17 + 1–4 days in culture) of the mouse cortex to investigate the different activity patterns of individual neurons in these regions. In the piriform cortex where SSA is initiated, a higher proportion of neurons was active asynchronously between waves, and a larger number of groups of coactive cells was present compared with the dorsal cortex. When we applied GABA and glutamate synaptic antagonists, asynchronous activity and cellular clusters remained, while synchronous activity was eliminated, indicating that asynchronous activity is a result of cell-intrinsic properties that differ between these regions. To test the hypothesis that higher levels of cell-autonomous activity in the piriform cortex underlie its ability to initiate waves, we constructed a conductance-based network model in which three layers differed only in the proportion of neurons able to intrinsically generate bursting behavior. Simulations using this model demonstrated that a gradient of intrinsic excitability was sufficient to produce directionally propagating waves that replicated key experimental features, indicating that the higher level of cell-intrinsic activity in the piriform cortex may provide a substrate for SSA generation.

scholarly journals Active information maintenance in working memory by a sensory cortex

2018 ◽  
Author(s):  
Xiaoxing Zhang ◽  
Wenjun Yan ◽  
Wenliang Wang ◽  
Hongmei Fan ◽  
Ruiqing Hou ◽  
...  
Keyword(s):  
Working Memory ◽  
Piriform Cortex ◽  
Delay Period ◽  
Sensory Cortex ◽  
Critical Function ◽  
Impaired Performance ◽  
Anterior Piriform Cortex ◽  
Electrophysiological Recordings ◽  
Dual Task Paradigm ◽  
The Brain

SummaryWorking memory is a critical function of the brain to maintain and manipulate information over delay periods of seconds. Sensory areas have been implicated in working memory; however, it is debated whether the delay-period activity of sensory regions is actively maintaining information or passively reflecting top-down inputs. We hereby examined the anterior piriform cortex, an olfactory cortex, in head-fixed mice performing a series of olfactory working memory tasks. Information maintenance is necessary in these tasks, especially in a dual-task paradigm in which mice are required to perform another distracting task while actively maintaining information during the delay period. Optogenetic suppression of the piriform cortex activity during the delay period impaired performance in all the tasks.Furthermore, electrophysiological recordings revealed that the delay-period activity of the anterior piriform cortex encoded odor information with or without the distracting task.Thus, this sensory cortex is critical for active information maintenance in working memory.

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