scholarly journals Tuning of ventral tenia tecta neurons of the olfactory cortex to distinct scenes of feeding behavior

2018 ◽  
Author(s):  
Kazuki Shiotani ◽  
Hiroyuki Manabe ◽  
Yuta Tanisumi ◽  
Koshi Murata ◽  
Junya Hirokawa ◽  
...  

AbstractVentral tenia tecta (vTT) is a part of the olfactory cortex that receives both olfactory sensory signals from the olfactory bulb and top-down signals from the prefrontal cortex. To address the question whether and how the neuronal activity of the vTT is modulated by prefrontal cognitive processes such as attention, expectation and working memory that occurs during goal-directed behaviors, we recorded individual neuronal responses in the vTT of freely moving awake mice that performed learned odor-guided feeding and drinking behaviors. We found that the firing pattern of individual vTT cells had repeatable behavioral correlates such that the environmental and behavioral scene the mouse encountered during the learned behavior was the major determinant of when individual vTT neurons fired maximally. Furthermore, spiking activity of these scene cells was modulated not only by the present scene but also by the future scene that the mouse predicted. We show that vTT receives afferent input from the olfactory bulb and top-down inputs from the medial prefrontal cortex and piriform cortex.These results indicate that different groups of vTT cells are activated at different scenes and suggest that processing of olfactory sensory information is handled by different scene cells during distinct scenes of learned feeding and drinking behaviors. In other words, during the feeding and drinking behavior, vTT changes its working mode moment by moment in accord with the scene change by selectively biasing specific scene cells. The scene effect on olfactory sensory processing in the vTT has implications for the neuronal circuit mechanisms of top-down attention and scene-dependent encoding and recall of olfactory memory.


2018 ◽  
Author(s):  
Donald A. Wilson ◽  
Maxime Juventin ◽  
Maria Ilina ◽  
Alessandro Pizzo ◽  
Catia Teixeira

AbstractActivity in sensory cortical networks reflects both peripheral sensory input and intra‐ and inter-cortical network input. How sensory cortices balance these diverse inputs to provide relatively stable, accurate representations of the external world is not well understood. Furthermore, neuromodulation could alter the balance of these inputs in a state‐ and behavior-dependent manner. Here, we used optogenetic stimulation to directly assay the relative strength of bottom-up (olfactory bulb) and top-down (lateral entorhinal cortex) synaptic inputs to piriform cortex in freely moving rats. Optotrodes in the piriform cortex were used to test the relative strength of these two inputs, in separate animals, with extracellular, monosynaptic evoked potentials. The results suggest a rapid state-dependent shift in the balance of bottom-up and top-down inputs to PCX, with enhancement in the strength of lateral entorhinal cortex synaptic input and stability or depression of olfactory bulb synaptic input during slow-wave sleep compared to waking. The shift is in part due to a state-dependent change in cholinergic tone as assessed with fiber photometry of GCaMP6 fluorescence in basal forebrain ChAT+ neurons, and blockade of the state-dependent synaptic shift with cholinergic muscarinic receptor activation.



1980 ◽  
Vol 28 (11) ◽  
pp. 1157-1169 ◽  
Author(s):  
D A Godfrey ◽  
C D Ross ◽  
J A Carter ◽  
O H Lowry ◽  
F M Matschinsky

Levels of the proposed neurotransmitter amino acids glutamate, aspartate, gamma-aminobutyric acid (GABA), and glycine were measured within the layered structures of the olfactory bulb and olfactory cortex following unilateral transections of the lateral olfactory tract or of virtually all fiber tracts of the olfactory peduncle. Distributions of the amino acids on both lesion and control sides were examined and compared by means of a mapping procedure. The results suggest: 1) Glutamate and aspartate are specifically associated with mitral (and presumably also tufted) cell axons and terminals in the piriform cortex. The distribution of aspartate in the olfactory bulb is further suggestive of a specific association of aspartate with mitral cell dendrites and somata. 2) Glutamate might be specifically associated with some centrifugal fibers traveling to the olfactory bulb in or near the anterior commissure. 3) GABA might be specifically related to some certrifugal fibers to the olfactory bulb in addition to its prominent association with granule cells of the bulb. 4) Glycine is unlikely to play a prominent neurotransmitter role in either the olfactory bulb or olfactory cortex.



2021 ◽  
Author(s):  
Zhen Chen ◽  
Krishnan Padmanabhan

In chemical sensation, multiple models have been proposed to explain how odors are represented by patterns of neuronal activity in the olfactory cortex. One hypothesis is that the identity of combinations of active neurons within specific sniff-related time windows are critical for encoding information about odors. Another model is that patterns of neural activity evolve across time and it is this temporal structure that is essential for encoding odor information. Interestingly, we found that top-down feedback to the olfactory bulb dictates what information is transmitted to the olfactory cortex by switching between these two strategies. Using a detailed model of the early olfactory system, we demonstrate that feedback control of inhibitory granule cells in the main olfactory bulb influences the balance between excitatory and inhibitory synaptic currents in mitral cells, thereby restructuring the firing patterns of piriform cortical cells across time. This resulted in performance gains in both the accuracy and reaction time of odor discrimination tasks. These findings lead us to propose a new framework for early olfactory computation, one in which top-down feedback to the bulb flexibly controls the temporal structure of neural activity in olfactory cortex, allowing the early olfactory system to dynamically switch between two distinct models of coding.  



2011 ◽  
Vol 31 (22) ◽  
pp. 8123-8133 ◽  
Author(s):  
H. Manabe ◽  
I. Kusumoto-Yoshida ◽  
M. Ota ◽  
K. Mori


2014 ◽  
Vol 40 (5) ◽  
pp. 2724-2733 ◽  
Author(s):  
Sayaka Komano-Inoue ◽  
Hiroyuki Manabe ◽  
Mizuho Ota ◽  
Ikue Kusumoto-Yoshida ◽  
Takeshi K. Yokoyama ◽  
...  


eLife ◽  
2017 ◽  
Vol 6 ◽  
Author(s):  
Benjamin Roland ◽  
Thomas Deneux ◽  
Kevin M Franks ◽  
Brice Bathellier ◽  
Alexander Fleischmann

Olfactory perception and behaviors critically depend on the ability to identify an odor across a wide range of concentrations. Here, we use calcium imaging to determine how odor identity is encoded in olfactory cortex. We find that, despite considerable trial-to-trial variability, odor identity can accurately be decoded from ensembles of co-active neurons that are distributed across piriform cortex without any apparent spatial organization. However, piriform response patterns change substantially over a 100-fold change in odor concentration, apparently degrading the population representation of odor identity. We show that this problem can be resolved by decoding odor identity from a subpopulation of concentration-invariant piriform neurons. These concentration-invariant neurons are overrepresented in piriform cortex but not in olfactory bulb mitral and tufted cells. We therefore propose that distinct perceptual features of odors are encoded in independent subnetworks of neurons in the olfactory cortex.



2020 ◽  
Author(s):  
Renata Medinaceli Quintela ◽  
Jennifer Bauer ◽  
Lutz Wallhorn ◽  
Daniela Brunert ◽  
Markus Rothermel

AbstractProcessing of sensory information is substantially modulated by centrifugal projections from higher cortical areas, yet their behavioral relevance and underlying neural mechanisms remain unclear in most cases. The anterior olfactory nucleus (AON) is part of the olfactory cortex and its extensive connections to lower and higher brain centers put it in a prime position to modulate early sensory information in the olfactory system. Here, we show that optogenetic activation of AON neurons in awake animals was not perceived as an odorant equivalent cue. However, AON activation during odorant presentation reliably suppressed odor responses. This AON mediated effect was fast and constant across odors and concentrations. Likewise, activation of glutamatergic AON projections to the olfactory bulb (OB) transiently inhibited the excitability of mitral/tufted cells (MTCs) that relay olfactory input to cortex. Single-unit MTC recordings revealed that optogenetic activation of glutamatergic AON terminals in the OB transiently decreased sensory-evoked MTC spiking, regardless of the strength or polarity of the sensory response. These findings suggest that glutamatergic AON projections to the OB suppress early olfactory processing by inhibiting OB output neurons and that the AON can dynamically gate sensory throughput to the cortex.Significance StatementThe anterior olfactory nucleus (AON) as an olfactory information processing area sends extensive projections to lower and higher brain centers but the behavioral consequences of its activation have been scarcely investigated. Using behavioral tests in combination with optogenetic manipulation we show that in contrast to what has been suggested previously, the AON does not seem to form odor percepts but instead suppresses odor responses across odorants and concentrations. Furthermore, this study shows that glutamatergic cortical projections to the olfactory bulb suppress olfactory processing by inhibiting output neurons, pointing to a potential mechanisms by which the olfactory cortex can actively and dynamically gate sensory throughput to higher brain centers.HighlightsAON stimulation suppresses odor responses across odorants and concentrationsAON activation is not perceived as an odorant equivalent cueThe AON dynamically shapes olfactory bulb output on a fast timescaleAON input to the olfactory bulb strongly suppresses mitral/tufted cells firing



2011 ◽  
Vol 71 ◽  
pp. e237
Author(s):  
Sayaka Komano ◽  
Hiroyuki Manabe ◽  
Mizuho Ota ◽  
Ikue Kusumoto-Yoshida ◽  
Takeshi Yokoyama ◽  
...  


2022 ◽  
Author(s):  
Magor L Lőrincz ◽  
Ildikó Piszár

Originating from the brainstem raphe nuclei, serotonin is an important neuromodulator involved in a variety of physiological and pathological functions. Specific optogenetic stimulation of serotonergic neurons results in the divisive suppression of spontaneous, but not sensory evoked activity in the majority of neurons in the primary olfactory cortex and an increase in firing in a minority of neurons. To reveal the mechanisms involved in this dual serotonergic control of cortical activity we used a combination of in vitro electrophysiological recordings from identified neurons in the primary olfactory cortex, optogenetics and pharmacology and found that serotonin suppressed the activity of principal neurons, but excited local interneurons. The results have important implications in sensory information processing and other functions of the olfactory cortex and related brain areas.



2011 ◽  
Author(s):  
J. Demanet ◽  
W. de Baene ◽  
C. C. Arrington ◽  
M. Brass


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