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Martin Deschênes

Publications and source records attributed to Martin Deschênes.

10 recordsLinked to original sources

Cholinergic modulation of vibrissal receptive fields in trigeminal nuclei.

In sensory systems, it is usually considered that mesopontine cholinergic neurons exert their modulatory action in the thalamus by enhancing the relay of sensory messages during states of neural network desynchronization. Here, we report a projection heretofore unknown of these cholinergic cells to the interpolar division of the brainstem trigeminal complex in rats. After FluoroGold injection in the interpolar nucleus, a number of retrogradely labeled cells were found bilaterally in the pedunculopontine tegmental nucleus, and immunostaining revealed that the vast majority of these cells were also positive for choline acetyltransferase. Immunostaining for the acetylcholine vesicular transporter confirmed the presence of cholinergic terminals in the interpolar nucleus, where electron microscopy showed that they make symmetric and asymmetric synaptic contacts with dendrites and axon terminals. In agreement with these anatomical data, recordings in slices showed that the cholinergic agonist carbachol depolarizes large-sized interpolaris cells and increases their excitability. Local application of carbachol in vivo enhances responses to adjacent whiskers, whereas systemic administration of the cholinergic antagonist scopolamine produces an opposite effect. Together, these results show that mesopontine cholinergic neurons exert a direct, effective control over receptive field size at the very first relay stations of the vibrissal system in rodents. As far as receptive field synthesis in the lemniscal pathway relies on intersubnuclear projections from the spinal complex, it follows that cholinergic modulation of sensory transmission in the interpolar nucleus will have a direct bearing on the type of messages that is forwarded to the thalamus and cerebral cortex.

Acetylcholine↗

Feedforward inhibitory control of sensory information in higher-order thalamic nuclei.

Sensory stimuli evoke strong responses in thalamic relay cells, which ensure a faithful relay of information to the neocortex. However, relay cells of the posterior thalamic nuclear group in rodents, despite receiving significant trigeminal input, respond poorly to vibrissa deflection. Here we show that sensory transmission in this nucleus is impeded by fast feedforward inhibition mediated by GABAergic neurons of the zona incerta. Intracellular recordings of posterior group neurons revealed that the first synaptic event after whisker deflection is a prominent inhibition. Whisker-evoked EPSPs with fast rise time and longer onset latency are unveiled only after lesioning the zona incerta. Excitation survives barrel cortex lesion, demonstrating its peripheral origin. Electron microscopic data confirm that trigeminal axons make large synaptic terminals on the proximal dendrites of posterior group cells and on the somata of incertal neurons. Thus, the connectivity of the system allows an unusual situation in which inhibition precedes ascending excitation resulting in efficient shunting of the responses. The dominance of inhibition over excitation strongly suggests that the paralemniscal pathway is not designed to relay inputs triggered by passive whisker deflection. Instead, we propose that this pathway operates through disinhibition, and that the posterior group forwards to the cerebral cortex sensory information that is contingent on motor instructions.

Action Potentials↗

The vibrissal system as a model of thalamic operations.

The highly segregated organization of the vibrissal system of rodents offers a unique opportunity to address key issues about thalamic operations in primary sensory and second order thalamic nuclei. In this short review, evidence showing that reticular thalamic neurons and relay cells with receptive fields on the same vibrissa form topographically closed loop connections has been summarized. Within whisker-related thalamic modules, termed barreloids, reticular axons synapse onto the cell bodies and dendrites of residing neurons as well as onto the distal dendrites of neurons that are located in adjacent barreloids. This arrangement provides a substrate for a mechanism of lateral inhibition whereby the spread of dendritic trees among surrounding barreloids determines whisker-specific patterns of lateral inhibition. The relay of sensory inputs in the posterior group, a second order nucleus associated with the vibrissal system is also examined. It is shown that in lightly anesthetized rats posterior group cells are tonically inhibited by GABAergic neurons of the ventral division of zona incerta. These observations suggest that a mechanism of disinhibition controls transmission of sensory signals in the posterior group nucleus. We further propose that disinhibition operates in a top-down manner, via motor instructions sent by cortex to brainstem and spinal cord. In this way posterior group nucleus would forward to the cerebral cortex sensory information that is contingent upon its action.

Afferent Pathways↗

Dendroarchitecture and lateral inhibition in thalamic barreloids.

Thalamic cells that relay vibrissa information to barrel cortex are clustered within whisker-related modules termed barreloids. Each barreloid receives input from one principal whisker and inhibitory inputs from reticular thalamic neurons with receptive fields that correspond to that same whisker. Although the proximal dendrites of relay cells are confined to their home barreloid, distal dendrites often extend into surrounding barreloids representing adjacent whiskers on the mystacial pad. It was proposed that this arrangement provides a substrate for a mechanism of lateral inhibition that operates remotely on extrabarreloid dendrites. In the present study, we identified adjacent whiskers that suppressed activity below background levels in barreloid cells, and we used a double-labeling protocol to relate the efficacy of inhibition to the dendroarchitecture of the cells. Significant suppression of background discharges was produced by 92% of adjacent whiskers within rows, by 48% of adjacent whiskers within arcs, but was never observed after deflection of nonadjacent whiskers. The magnitude of lateral inhibition increases linearly as the cumulated length of dendrites increases in the barreloid representing an adjacent whisker (R2 = 0.86; p < 0.0001). As distance between cell bodies and the border of an adjacent barreloid increases, dendritic length in that adjacent barreloid diminishes and so does inhibition. Considering time differences between the arrival of principal and adjacent whisker inputs in barreloids, our data suggest that inhibition operating distally on dendrites acts as a spatial filter that primarily suppresses adjacent whisker inputs and so contributes to enhance edge detection.

Anesthesia↗

Synthesis of multiwhisker-receptive fields in subcortical stations of the vibrissa system.

This study addresses the origins of multiwhisker-receptive fields of neurons in the thalamic ventral posterior medial (VPM) nucleus of the rat. We sought to determine whether multiwhisker-receptive field synthesis occurs in VPM through convergent projections from the principalis (PrV) and interpolaris (SpVi) nuclei, or in PrV by intersubnuclear projections from the spinal trigeminal complex. We tested these hypotheses by recording whisker-evoked responses in PrV and VPM before and after electrolytic lesion of the SpVi in lightly anesthetized rats. Before the lesion PrV cells responded, on average, to 3.2 +/- 1.2 whiskers but responsiveness was reduced to 1.07 +/- 0.31 whisker after the lesion. A similar reduction of receptive field size was observed in VPM, where neurons responded, on average, to 2.94 +/- 0.95 whiskers before the lesion and to 1.05 +/- 0.22 whisker after the lesion. Thus one can conclude that intersubnuclear projections mediate surround whisker-receptive fields in PrV, and therefore in VPM. However, it has previously been shown that parasagittal brain stem transection, which severed ascending projections from SpVi, but left intersubnuclear connections intact, rendered VPM cells monowhisker responsive. We wondered whether midline brain stem lesion modified receptive field properties in SpVi. In normal rats SpVi cells responded, on average, to 7.52 +/- 4.25 whiskers, but responsiveness was dramatically reduced to 1.47 +/- 1.07 whisker after the lesion. Together these results indicate that the synthesis of surround receptive fields in subcortical stations relies almost exclusively on intersubnuclear projections from the spinal trigeminal complex to the PrV.

Animals↗

A map of angular tuning preference in thalamic barreloids.

A double-labeling protocol was used to determine how cells with different angular preferences to whisker motion distribute across the dimensions of a barreloid in the ventral posterior medial nucleus of the rat thalamus. Individual barreloids were labeled retrogradely by injecting Fluoro-Gold in identified barrel columns, and single relay cells (n = 30) pertaining to the labeled barreloids were stained juxtacellularly with Neurobiotin after determination of their angular tuning preference to controlled whisker deflection. Results show that cells with like angular preference are clustered within the barreloids. Those best tuned to forward and upward directions are located principally in the dorsal sector of the barreloid, whereas those best tuned to backward and downward motion are located principally in the central and ventral sectors, respectively. The relationship between cell location and angular preference was assessed by regression, cluster, and discriminant analysis. Together, these tests indicate that barreloids contain a map of shifting angular preference that transposes along the length of a barreloid directional property imposed at the periphery by the circumferential distribution of receptors around the vibrissa follicles.

Action Potentials↗

Single-cell study of motor cortex projections to the barrel field in rats.

In freely moving rats, whisking is associated with a slow modulation of neuronal excitability in the primary somatosensory cortex. Because it persists after the blockade of vibrissa input, it was suggested that the slow modulation might be mediated by motor-sensory corticocortical connections and perhaps result from the corollary discharges of corticofugal cells. In the present study, we identified motor cortical cells that project to the barrel field and reconstructed their axonal projections after juxtacellularly staining single cells with a biotinylated tracer. On the basis of the final destination of main axons, two groups of neurons contribute to motor-sensory projections: callosal cells (87.5%) and corticofugal cells (12.5%). Axon collaterals of callosal cells arborize in layers five to six of the granular and dysgranular zones and give off several branches that ascend between the barrels to ramify in the molecular layer. In contrast, the axon collaterals of corticofugal cells do not ramify in the infragranular layers but in layer 1. The origin of the majority of motor sensory projections from callosally projecting cells does not support the notion that the slow modulation results from the corollary discharges of corticofugal axons. It would rather originate from a separate population of cells, which could output the slow signal to the barrel field in parallel with the corticofugal commands to a brainstem pattern generator. As free whisking is characterized by bilateral concerted movements of the vibrissae, the transcallosal contribution of motor-sensory axons represents a substrate for synchronizing the slow modulation across both hemispheres.

Animals↗

The relay of high-frequency sensory signals in the Whisker-to-barreloid pathway.

The present study investigated the operational features of whisker-evoked EPSPs in barreloid cells and the ability of the whisker-to-barreloid pathway to relay high rates of whisker deflection in lightly anesthetized rats. Results show that lemniscal EPSPs are single-fiber events with fast rise times (<500 microsec) that strongly depress at short inter-EPSP intervals. They occur at short latencies (3.84 +/- 0.96 msec) with little jitters (<300 microsec) after electrical stimulation of the whisker follicle. Waveform analysis indicates that one to three lemniscal axons converge on individual barreloid cells to produce EPSPs of similar rise times but different amplitudes. When challenged by high rates of whisker deflection, cells in the whisker-to-barreloid pathway demonstrate a remarkable frequency-following ability. Primary vibrissa afferents could follow in a phase-locked manner trains of sinusoidal deflections at up to 1 kHz. Although trigeminothalamic cells could still faithfully follow deflection rates of 200-300 Hz, the actual frequency-following ability of individual cells depends on the amplitude, velocity, and direction of displacements. The discharges of trigeminothalamic cells induce corresponding phase-locked EPSPs in barreloid cells, which trigger burst discharges at stimulus onset. During the following cycles of the stimulus train, few action potentials ensue because of the strong synaptic depression at lemniscal synapses. It is concluded that the whisker-to-barreloid pathway can relay vibratory inputs with a high degree of temporal precision, but that the relay of this information to the cerebral cortex requires the action of modulators, and possibly phase-locked discharges among an ensemble of relay cells.

Animals↗

Dendroarchitecture of relay cells in thalamic barreloids: a substrate for cross-whisker modulation.

A double-labeling protocol was used to determine how the dendroarchitecture of relay cells relates to the three-dimensional structure of barreloids in the ventral posterior medial nucleus of the rat thalamus. Single barreloids were retrogradely labeled by injecting Fluoro-Gold in identified barrel columns, and single relay cells activated by the same whisker, or by an adjacent whisker located on the same arc, were juxtacellularly labeled with biotinylated dextran. Results show that the dendritic field of relay cells is asymmetric, variously oriented with respect to the geometry of the barreloids, and that all cells extend dendrites in surrounding barreloids. Extrabarreloid dendrites are of small size (<1.5 microm) and represent up to 54% (range, 11-54%) of the total dendritic length. In contrast, the thick proximal dendrites remain confined to the home barreloid of the cell, being directed toward its center or along its margin. There is a trend for cells located dorsally in barreloids to form more elaborate trees with a larger proportion of extrabarreloid dendrites. Electron microscopic examination of labeled cells shows that extrabarreloid dendrites are exclusively contacted by synaptic terminals of cortical and reticular thalamic origin, whereas intrabarreloid dendrites also receive contacts from lemniscal terminals. Because corticothalamic and reticular thalamic cells establish point-to-point connections with homotopic barreloids, it is proposed that the spatial arrangement of dendrites determines the combination of whisker deflection that best modulates cell firing. Because relay cell responses are direction sensitive, maximal modulation would occur if dendritic field orientation relates to the direction selectivity of responses.

Afferent Pathways↗

Substrate for cross-talk inhibition between thalamic barreloids.

A double-labeling protocol was used to determine whether thalamocortical and reticular thalamic cells with overlapping receptive fields form open or closed loop connections in the vibrissal system of the rat. Results show that individual reticular cells exclusively project to the barreloid representing the principal whisker of their receptive field. Furthermore, solid retrograde labeling of relay cells reveals that a large number extend dendrites outside their home barreloid. This feature, together with previous demonstrations that reticular thalamic axons principally contact the dendrites of relay cells, provide a morphological substrate for cross-talk inhibition between thalamic barreloids.

Animals↗