Spatiotemporal Characteristics of Neuronal Sensory Integration in the Barrel Cortex of the Rat

2005 ◽  
Vol 93 (3) ◽  
pp. 1450-1467 ◽  
Author(s):  
Valérie Ego-Stengel ◽  
Tadeu Mello E Souza ◽  
Vincent Jacob ◽  
Daniel E. Shulz
Keyword(s):  
Barrel Cortex ◽  
Temporal Frequency ◽  
Spatial Arrangement ◽  
Spatiotemporal Pattern ◽  
Time Interval ◽  
Response Modulation ◽  
Neuronal Responses ◽  
Rapid Sequence ◽  
Sensory Cortices ◽  
Stimulation Of

In primary sensory cortices, neuronal responses to a stimulus presented as part of a rapid sequence often differ from responses to an isolated stimulus. It has been reported that sequential stimulation of two whiskers produces facilitatory modulations of barrel cortex neuronal responses. These results are at odds with the well-known suppressive interaction that has been usually described. Herein, we have examined the dependency of response modulation on the spatiotemporal pattern of stimulation by varying the spatial arrangement of the deflected vibrissae, the temporal frequency of stimulation, and the time interval between whisker deflections. Extracellular recordings were made from primary somatosensory cortex of anesthetized rats. Two contralateral whiskers were stimulated at 0.5 and 8 Hz at intervals ranging from 0 to ±30 ms. Response interactions were assessed during stimulation of the principal and adjacent whiskers, first from the same row and second from the same arc. When tested at 0.5 Hz, 59% of single units showed a statistically significant suppressive interaction, whereas response facilitation was found in only 6% of cells. In contrast, at 8 Hz, a significant supralinear summation was observed in 19% of the cells, particularly for stimulations along an arc rather than along a row. Multi-unit recordings showed similar results. These observations indicate that most of the interactions in the barrel cortex during two-whisker stimulation are suppressive. However, facilitation can be revealed when stimuli are applied at a physiological frequency and could be the basis for internal representations of the spatiotemporal pattern of the stimulus.

Similarity of Direction Tuning Among Responses to Stimulation of Different Whiskers in Neurons of Rat Barrel Cortex

2005 ◽  
Vol 94 (3) ◽  
pp. 2004-2018 ◽  
Author(s):  
Hiroyuki Kida ◽  
Satoshi Shimegi ◽  
Hiromichi Sato
Keyword(s):  
Barrel Cortex ◽  
Direction Selectivity ◽  
Specific Response ◽  
Neuronal Responses ◽  
Preferred Direction ◽  
Fast Spiking ◽  
Whisker Stimulation ◽  
Direction Tuning ◽  
Network Mechanism ◽  
Stimulation Of

Cells in the rat barrel cortex exhibit stimulus-specific response properties. To understand the network mechanism of direction selectivity in response to facial whisker deflection, we examined direction selectivity of neuronal responses to single- and multiwhisker stimulations. In the case of regular-spiking units, i.e., putative excitatory cells, direction preferences were quite similar between responses to single-whisker stimulation of the principal and adjacent whiskers. In multiwhisker stimulation at short (≤5 ms) interstimulus intervals (ISIs), response facilitation was evoked only when the whiskers were deflected to the preferred direction of the response to the single whisker stimulation. These results suggest that there are neuronal networks among cells with different whisker preferences but with a common direction preference that could be the neuronal basis of the direction-selective facilitation of the response to multiwhisker stimulation. In contrast, multiwhisker stimulation at long (≥6 ms) ISIs caused non–direction-selective suppression of the response to the second stimulus. In the case of fast-spiking units, i.e., putative inhibitory cells, poor direction selectivity was exhibited. Thus stimulus direction is represented as the direction-selective responses to the single- and multiwhisker stimulations of putative excitatory cells rather than those of putative inhibitory cells.

scholarly journals Acetylcholine-Dependent Induction and Expression of Functional Plasticity in the Barrel Cortex of the Adult Rat

2001 ◽  
Vol 86 (1) ◽  
pp. 422-437 ◽  
Author(s):  
Valérie Ego-Stengel ◽  
Daniel E. Shulz ◽  
Sebastian Haidarliu ◽  
Ronen Sosnik ◽  
Ehud Ahissar
Keyword(s):  
Molecular Mechanisms ◽  
Barrel Cortex ◽  
Temporal Frequency ◽  
Stimulus Frequency ◽  
Sequential Presentation ◽  
Adult Rat ◽  
Temporal Properties ◽  
Sensory Plasticity ◽  
Cumulative Process ◽  
Stimulation Of

The involvement of acetylcholine (ACh) in the induction of neuronal sensory plasticity is well documented. Recently we demonstrated in the somatosensory cortex of the anesthetized rat that ACh is also involved in the expression of neuronal plasticity. Pairing stimulation of the principal whisker at a fixed temporal frequency with ACh iontophoresis induced potentiations of response that required re-application of ACh to be expressed. Here we fully characterize this phenomenon and extend it to stimulation of adjacent whiskers. We show that these ACh-dependent potentiations are cumulative and reversible. When several sensori-cholinergic pairings were applied consecutively with stimulation of the principal whisker, the response at the paired frequency was further increased, demonstrating a cumulative process that could reach saturation levels. The potentiations were specific to the stimulus frequency: if the successive pairings were done at different frequencies, then the potentiation caused by the first pairing was depotentiated, whereas the response to the newly paired frequency was potentiated. During testing, the potentiation of response did not develop immediately on the presentation of the paired frequency during application of ACh: the analysis of the kinetics of the effect indicates that this process requires the sequential presentation of several trains of stimulation at the paired frequency to be expressed. We present evidence that a plasticity with similar characteristics can be induced for responses to stimulation of an adjacent whisker, suggesting that this potentiation could participate in receptive field spatial reorganizations. The spatial and temporal properties of the ACh-dependent plasticity presented here impose specific constraints on the underlying cellular and molecular mechanisms.

Spatio-temporal visual properties in the ascending tectofugal system

2010 ◽  
Vol 5 (1) ◽  
pp. 21-30 ◽  
Author(s):  
Alice Rokszin ◽  
Zita Márkus ◽  
Gábor Braunitzer ◽  
Antal Berényi ◽  
Marek Wypych ◽  
...  
Keyword(s):  
Visual Information ◽  
Frequency Tuning ◽  
Temporal Frequency ◽  
Neuronal Population ◽  
Neuronal Responses ◽  
Temporal Properties ◽  
Visual Receptive Field ◽  
Detailed Statistical Analysis ◽  
Spatio Temporal ◽  
Visual Properties

AbstractOur study compares the spatio-temporal visual receptive field properties of different subcortical stages of the ascending tectofugal visual system. Extracellular single-cell recordings were performed in the superficial (SCs) and intermediate (SCi) layers of the superior colliculus (SC), the suprageniculate nucleus (Sg) of the posterior thalamus and the caudate nucleus (CN) of halothane-anesthetized cats. Neuronal responses to drifting gratings of various spatial and temporal frequencies were recorded. The neurons of each structure responded optimally to low spatial and high temporal frequencies and displayed narrow spatial and temporal frequency tuning. The detailed statistical analysis revealed that according to its stimulus preferences the SCs has markedly different spatio-temporal properties from the homogeneous group formed by the SCi, Sg and CN. The SCs neurons preferred higher spatial and lower temporal frequencies and had broader spatial tuning than the other structures. In contrast to the SCs the visually active SCi, as well as the Sg and the CN neurons possessed consequently similar spatio-temporal preferences. These data support our hypothesis that the visually active SCi, Sg and CN neurons form a homogeneous neuronal population given a similar spatio-temporal frequency preference and a common function in processing of dynamic visual information.

Olfactory modulation of barrel cortex activity during active whisking and passive whisker stimulation

2021 ◽  
Author(s):  
Anthony Renard ◽  
Evan Harrell ◽  
Brice Bathallier
Keyword(s):  
Facial Nerve ◽  
Calcium Imaging ◽  
Tactile Stimulation ◽  
Barrel Cortex ◽  
Neuronal Responses ◽  
Population Activity ◽  
Tactile Information ◽  
Large Populations ◽  
Whisker Stimulation ◽  
The Impact

Abstract Rodents depend on olfaction and touch to meet many of their fundamental needs. The joint significance of these sensory systems is underscored by an intricate coupling between sniffing and whisking. However, the impact of simultaneous olfactory and tactile inputs on sensory representations in the cortex remains elusive. To study these interactions, we recorded large populations of barrel cortex neurons using 2-photon calcium imaging in head-fixed mice during olfactory and tactile stimulation. We find that odors alter barrel cortex activity in at least two ways, first by enhancing whisking, and second by central cross-talk that persists after whisking is abolished by facial nerve sectioning. Odors can either enhance or suppress barrel cortex neuronal responses, and while odor identity can be decoded from population activity, it does not interfere with the tactile representation. Thus, barrel cortex represents olfactory information which, in the absence of learned associations, is coded independently of tactile information.

Influences from laryngeal afferents on expiratory bulbospinal neurons and motoneurons

1988 ◽  
Vol 64 (4) ◽  
pp. 1337-1345 ◽  
Author(s):  
J. S. Jodkowski ◽  
A. J. Berger
Keyword(s):  
Electrical Stimulation ◽  
Cold Water ◽  
Superior Laryngeal Nerve ◽  
Intercostal Nerve ◽  
Firing Frequency ◽  
Neuronal Responses ◽  
Water Infusion ◽  
Afferent Activation ◽  
Expiratory Neurons ◽  
Stimulation Of

The purpose of this study is to analyze the reflex effects of laryngeal afferent activation on respiratory patterns in anesthetized, vagotomized, paralyzed, ventilated cats. We recorded simultaneously from the phrenic nerve, T10 internal intercostal nerve, and single bulbospinal expiratory neurons of the caudal ventral respiratory group (VRG). Laryngeal afferents were activated by electrical stimulation of the superior laryngeal nerve (SLN) or by cold-water infusion into the larynx. Both types of stimuli caused inhibition of phrenic activity and facilitation of internal intercostal nerve activity, indicating expiratory effort. The activity of 46 bulbospinal expiratory cells was depressed during SLN electrical stimulation, and 13 of them were completely inhibited. In 44 of 56 neurons tested, mean firing frequency (FFmean) was decreased in response to cold-water infusion and 8 others responded with increased FFmean; in the remaining 4 neurons, FFmean was unchanged. Possible reasons for different neuronal responses to SLN electrical stimulation and water infusion are discussed. We conclude that bulbospinal expiratory neurons of VRG were not the source of the reflex motoneuronal expiratory-like activity produced by SLN stimulation. Other, not yet identified inputs to spinal expiratory motoneurons are activated during this experimental condition.

Brain stem responses to electrical stimulation of ventral vagal gastric fibers

1989 ◽  
Vol 257 (1) ◽  
pp. G24-G29
Author(s):  
W. D. Barber ◽  
C. S. Yuan
Keyword(s):  
Electrical Stimulation ◽  
Brain Stem ◽  
Time Of Arrival ◽  
Neuronal Responses ◽  
Proximal Stomach ◽  
Afferent Fibers ◽  
Sensory Modalities ◽  
The Mean ◽  
The Brain ◽  
Stimulation Of

The brain stem neuronal responses to electrical stimulation of gastric branches of the ventral vagal trunk serving the proximal stomach were localized and evaluated in anesthetized cats. The responses were equally distributed bilaterally in the region of nucleus solitarius in the caudal brain stem. The mean latency of the response was 289 +/- 46 (SD) ms, which translated into a conduction velocity of less than 1 m/s based on the distance between the stimulating and recording electrodes. The responses consisted of single and multiple spikes that showed slight variability in the latency, indicating orthodromic activation via a synapse in approximately 98% of the responses recorded. Forty two percent of the units tested showed evidence of convergence of input from vagal afferent fibers in different branches of the ventral vagal trunk that served the proximal stomach. The resultant activity pattern of the unitary response appeared to be the product of 1) the gastric sensory input or modality conveyed by the afferent source and 2) the time of arrival and diversity of modalities served by other gastric afferents impinging on the unit. This provides a mechanism capable of responding on the basis of specific sensory modalities that dynamically reflect ongoing events monitored and conveyed by other gastric afferents in the region.

scholarly journals Effects of left stellate ganglion stimulation on left ventricular synchrony in dogs

1964 ◽  
Vol 207 (1) ◽  
pp. 181-186 ◽  
Author(s):  
Charles E. Osadjan ◽  
Walter C. Randall
Keyword(s):  
Electromechanical Coupling ◽  
Interventricular Septum ◽  
Stellate Ganglion ◽  
Left Ventricular ◽  
Cardiac Response ◽  
Time Interval ◽  
Ventricular Synchrony ◽  
Left Stellate Ganglion ◽  
Coupling Time ◽  
Stimulation Of

The cardiac response to excitation via the sympathetics has led to the inference that improved synchrony of contraction in the ventricular musculature is important to augmented performance. Pin electrodes and strain-gauge arches were fixed to several segments of the left ventricle, and the precise sequence of electrical excitation and mechanical shortening of the septum and epicardial segments of the apex and base compared during control periods and during electrical stimulation of the left stellate ganglion. During stimulation, augmentation in force of contraction was recorded from all segments, including the interventricular septum. In controls, one-half showed initial shortening at the apex and one-half at the base. During stimulation of the stellate, the base contracted first, and the electromechanical coupling time decreased significantly. The septum shortened last in all circumstances. The time interval between the first and the last segment to shorten decreased during stimulation, indicating increased synchrony of contraction. This undoubtedly contributes to the more rapid rise phase of the ventricular pressure pulse during sympathetic stimulation.

Administration of AVP to the area postrema alters response of NTS neurons to afferent inputs

1997 ◽  
Vol 272 (2) ◽  
pp. R519-R525 ◽  
Author(s):  
L. Qu ◽  
M. Hay ◽  
V. S. Bishop
Keyword(s):  
Vagal Stimulation ◽  
Area Postrema ◽  
Arterial Baroreflex ◽  
Neuronal Responses ◽  
Aortic Depressor Nerve ◽  
Before And After ◽  
Venous Infusion ◽  
The Mean ◽  
Afferent Inputs ◽  
Stimulation Of

This study was designed to determine if arginine vasopressin (AVP) facilitates the response of nucleus of the solitary tract (NTS) neurons to baroreceptor input. In anesthetized sinoaortic-denervated vagotomized rabbits, AVP was intravenously infused (15 microg x kg(-1) x min(-1), 1 min) or microinjected into the area postrema (AP; 1 ng/nl, 10 nl). Extracellular recordings of evoked NTS neuronal responses to electrical stimulation of the aortic depressor nerve (ADN) or vagus nerve (1 Hz, 2-20 V, 0.05-0.6 ms) were evaluated before and after AVP administration. In neurons receiving input from the ADN (n = 19), 58% of them increased their responses after AVP (40.3 +/- 5.0 to 71.5 +/- 4,8%, P < 0.001). Similarly, in neurons activated by vagal stimulation (n = 22), 55% of them were facilitated during AVP administration (59.7 +/- 12.8 to 90.8 +/- 10.7%, P < 0.01). This action of AVP was independent of the mode of AVP administration, since either microinjection or venous infusion was effective in augmenting responses of NTS neurons to aortic/vagal stimulation. In an additional 37 spontaneous NTS neurons, AVP showed no effect on the mean baseline firing rate (8.9 +/- 1.3 vs. 9.6 +/- 1.3 spikes/s, P > 0.05), but increased neuronal activity in 54% of neurons (6.9 +/- 1.3 vs. 13.1 +/- 1.7 spikes/s, P < 0.01). In two rabbits pretreated with vasopressin antagonist (15 microg/kg iv), AVP failed to produce facilitatory effects (n = 8). The results of this study provide evidence in support of the hypothesis that circulating peptides modulate the arterial baroreflex via activation of neurons in the AP.

scholarly journals Voltage-sensitive dye imaging reveals shifting spatiotemporal spread of whisker-induced activity in rat barrel cortex

2013 ◽  
Vol 109 (9) ◽  
pp. 2382-2392 ◽  
Author(s):  
Brian R. Lustig ◽  
Robert M. Friedman ◽  
Jeremy E. Winberry ◽  
Ford F. Ebner ◽  
Anna W. Roe
Keyword(s):  
Barrel Cortex ◽  
Sensory Information ◽  
Population Level ◽  
Spatiotemporal Pattern ◽  
Voltage Sensitive Dye ◽  
Barrel Field ◽  
Spatial Shift ◽  
Response Peak ◽  
Whisker Stimulation ◽  
Spike Firing

In rats, navigating through an environment requires continuous information about objects near the head. Sensory information such as object location and surface texture are encoded by spike firing patterns of single neurons within rat barrel cortex. Although there are many studies using single-unit electrophysiology, much less is known regarding the spatiotemporal pattern of activity of populations of neurons in barrel cortex in response to whisker stimulation. To examine cortical response at the population level, we used voltage-sensitive dye (VSD) imaging to examine ensemble spatiotemporal dynamics of barrel cortex in response to stimulation of single or two adjacent whiskers in urethane-anesthetized rats. Single whisker stimulation produced a poststimulus fluorescence response peak within 12–16 ms in the barrel corresponding to the stimulated whisker (principal whisker). This fluorescence subsequently propagated throughout the barrel field, spreading anisotropically preferentially along a barrel row. After paired whisker stimulation, the VSD signal showed sublinear summation (less than the sum of 2 single whisker stimulations), consistent with previous electrophysiological and imaging studies. Surprisingly, we observed a spatial shift in the center of activation occurring over a 10- to 20-ms period with shift magnitudes of 1–2 barrels. This shift occurred predominantly in the posteromedial direction within the barrel field. Our data thus reveal previously unreported spatiotemporal patterns of barrel cortex activation. We suggest that this nontopographical shift is consistent with known functional and anatomic asymmetries in barrel cortex and that it may provide an important insight for understanding barrel field activation during whisking behavior.

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