Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 126
Filter
1.
Nature ; 608(7921): 146-152, 2022 08.
Article in English | MEDLINE | ID: mdl-35831500

ABSTRACT

Social affiliation emerges from individual-level behavioural rules that are driven by conspecific signals1-5. Long-distance attraction and short-distance repulsion, for example, are rules that jointly set a preferred interanimal distance in swarms6-8. However, little is known about their perceptual mechanisms and executive neural circuits3. Here we trace the neuronal response to self-like biological motion9,10, a visual trigger for affiliation in developing zebrafish2,11. Unbiased activity mapping and targeted volumetric two-photon calcium imaging revealed 21 activity hotspots distributed throughout the brain as well as clustered biological-motion-tuned neurons in a multimodal, socially activated nucleus of the dorsal thalamus. Individual dorsal thalamus neurons encode local acceleration of visual stimuli mimicking typical fish kinetics but are insensitive to global or continuous motion. Electron microscopic reconstruction of dorsal thalamus neurons revealed synaptic input from the optic tectum and projections into hypothalamic areas with conserved social function12-14. Ablation of the optic tectum or dorsal thalamus selectively disrupted social attraction without affecting short-distance repulsion. This tectothalamic pathway thus serves visual recognition of conspecifics, and dissociates neuronal control of attraction from repulsion during social affiliation, revealing a circuit underpinning collective behaviour.


Subject(s)
Crowding , Neurons , Social Behavior , Superior Colliculi , Thalamus , Visual Pathways , Zebrafish , Animals , Brain Mapping , Calcium/analysis , Hypothalamus/cytology , Hypothalamus/physiology , Locomotion , Microscopy, Electron , Neurons/cytology , Neurons/physiology , Neurons/ultrastructure , Pattern Recognition, Visual , Photic Stimulation , Superior Colliculi/cytology , Superior Colliculi/physiology , Thalamus/cytology , Thalamus/physiology , Visual Pathways/cytology , Visual Pathways/physiology , Visual Pathways/ultrastructure , Zebrafish/physiology
2.
PLoS Comput Biol ; 17(11): e1009181, 2021 11.
Article in English | MEDLINE | ID: mdl-34723955

ABSTRACT

Sensory information from different modalities is processed in parallel, and then integrated in associative brain areas to improve object identification and the interpretation of sensory experiences. The Superior Colliculus (SC) is a midbrain structure that plays a critical role in integrating visual, auditory, and somatosensory input to assess saliency and promote action. Although the response properties of the individual SC neurons to visuoauditory stimuli have been characterized, little is known about the spatial and temporal dynamics of the integration at the population level. Here we recorded the response properties of SC neurons to spatially restricted visual and auditory stimuli using large-scale electrophysiology. We then created a general, population-level model that explains the spatial, temporal, and intensity requirements of stimuli needed for sensory integration. We found that the mouse SC contains topographically organized visual and auditory neurons that exhibit nonlinear multisensory integration. We show that nonlinear integration depends on properties of auditory but not visual stimuli. We also find that a heuristically derived nonlinear modulation function reveals conditions required for sensory integration that are consistent with previously proposed models of sensory integration such as spatial matching and the principle of inverse effectiveness.


Subject(s)
Models, Neurological , Superior Colliculi/physiology , Acoustic Stimulation , Animals , Auditory Perception/physiology , Brain Mapping/statistics & numerical data , Computational Biology , Electrophysiological Phenomena , Female , Male , Mice , Mice, Inbred CBA , Models, Psychological , Neurons/physiology , Nonlinear Dynamics , Photic Stimulation , Sensation/physiology , Superior Colliculi/cytology , Visual Perception/physiology
3.
J Neurosci ; 40(27): 5228-5246, 2020 07 01.
Article in English | MEDLINE | ID: mdl-32444386

ABSTRACT

Humans and animals maintain accurate sound discrimination in the presence of loud sources of background noise. It is commonly assumed that this ability relies on the robustness of auditory cortex responses. However, only a few attempts have been made to characterize neural discrimination of communication sounds masked by noise at each stage of the auditory system and to quantify the noise effects on the neuronal discrimination in terms of alterations in amplitude modulations. Here, we measured neural discrimination between communication sounds masked by a vocalization-shaped stationary noise from multiunit responses recorded in the cochlear nucleus, inferior colliculus, auditory thalamus, and primary and secondary auditory cortex at several signal-to-noise ratios (SNRs) in anesthetized male or female guinea pigs. Masking noise decreased sound discrimination of neuronal populations in each auditory structure, but collicular and thalamic populations showed better performance than cortical populations at each SNR. In contrast, in each auditory structure, discrimination by neuronal populations was slightly decreased when tone-vocoded vocalizations were tested. These results shed new light on the specific contributions of subcortical structures to robust sound encoding, and suggest that the distortion of slow amplitude modulation cues conveyed by communication sounds is one of the factors constraining the neuronal discrimination in subcortical and cortical levels.SIGNIFICANCE STATEMENT Dissecting how auditory neurons discriminate communication sounds in noise is a major goal in auditory neuroscience. Robust sound coding in noise is often viewed as a specific property of cortical networks, although this remains to be demonstrated. Here, we tested the discrimination performance of neuronal populations at five levels of the auditory system in response to conspecific vocalizations masked by noise. In each acoustic condition, subcortical neurons better discriminated target vocalizations than cortical ones and in each structure, the reduction in discrimination performance was related to the reduction in slow amplitude modulation cues.


Subject(s)
Animal Communication , Auditory Perception/physiology , Discrimination, Psychological/physiology , Noise , Vocalization, Animal/physiology , Acoustic Stimulation , Algorithms , Animals , Auditory Cortex/cytology , Auditory Cortex/physiology , Female , Guinea Pigs , Male , Perceptual Masking , Signal-To-Noise Ratio , Superior Colliculi/cytology , Superior Colliculi/physiology , Thalamus/cytology , Thalamus/physiology
4.
Nat Commun ; 11(1): 1087, 2020 02 27.
Article in English | MEDLINE | ID: mdl-32107385

ABSTRACT

Sound localization plays a critical role in animal survival. Three cues can be used to compute sound direction: interaural timing differences (ITDs), interaural level differences (ILDs) and the direction-dependent spectral filtering by the head and pinnae (spectral cues). Little is known about how spectral cues contribute to the neural encoding of auditory space. Here we report on auditory space encoding in the mouse superior colliculus (SC). We show that the mouse SC contains neurons with spatially-restricted receptive fields (RFs) that form an azimuthal topographic map. We found that frontal RFs require spectral cues and lateral RFs require ILDs. The neurons with frontal RFs have frequency tunings that match the spectral structure of the specific head and pinna filter for sound coming from the front. These results demonstrate that patterned spectral cues in combination with ILDs give rise to the topographic map of azimuthal auditory space.


Subject(s)
Auditory Pathways/physiology , Cues , Sound Localization/physiology , Superior Colliculi/physiology , Acoustic Stimulation , Animals , Auditory Pathways/cytology , Brain Mapping/methods , Ear Auricle/physiology , Electrodes, Implanted , Female , Male , Mice , Neurons/physiology , Superior Colliculi/cytology
5.
J Neurosci ; 39(23): 4576-4594, 2019 06 05.
Article in English | MEDLINE | ID: mdl-30936242

ABSTRACT

An innocuous sensory stimulus that reliably signals an upcoming aversive event can be conditioned to elicit locomotion to a safe location before the aversive outcome ensues. The neural circuits that mediate the expression of this signaled locomotor action, known as signaled active avoidance, have not been identified. While exploring sensorimotor midbrain circuits in mice of either sex, we found that excitation of GABAergic cells in the substantia nigra pars reticulata blocks signaled active avoidance by inhibiting cells in the pedunculopontine tegmental nucleus (PPT), not by inhibiting cells in the superior colliculus or thalamus. Direct inhibition of putative-glutamatergic PPT cells, excitation of GABAergic PPT cells, or excitation of GABAergic afferents in PPT, abolish signaled active avoidance. Conversely, excitation of putative-glutamatergic PPT cells, or inhibition of GABAergic PPT cells, can be tuned to drive avoidance responses. The PPT is an essential junction for the expression of signaled active avoidance gated by nigral and other synaptic afferents.SIGNIFICANCE STATEMENT When a harmful situation is signaled by a sensory stimulus (e.g., street light), subjects typically learn to respond with active or passive avoidance responses that circumvent the threat. During signaled active avoidance behavior, subjects move away to avoid a threat signaled by a preceding innocuous stimulus. We identified a part of the midbrain essential to process the signal and avoid the threat. Inhibition of neurons in this area eliminates avoidance responses to the signal but preserves escape responses caused by presentation of the threat. The results highlight an essential part of the neural circuits that mediate signaled active avoidance behavior.


Subject(s)
Avoidance Learning/physiology , Escape Reaction/physiology , GABAergic Neurons/physiology , Nerve Net/physiology , Pars Reticulata/physiology , Pedunculopontine Tegmental Nucleus/physiology , Animals , Avoidance Learning/drug effects , Avoidance Learning/radiation effects , Brain Mapping , Carrier Proteins/genetics , Carrier Proteins/radiation effects , Clozapine/analogs & derivatives , Clozapine/pharmacology , Conditioning, Classical , Dependovirus/genetics , Drinking Behavior , Electroshock , Escape Reaction/drug effects , Escape Reaction/radiation effects , Gain of Function Mutation , Genes, Reporter , Genetic Vectors/administration & dosage , Light , Mice , Noise/adverse effects , Optogenetics , Pars Reticulata/cytology , Reaction Time , Receptors, G-Protein-Coupled/genetics , Receptors, G-Protein-Coupled/radiation effects , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/radiation effects , Superior Colliculi/cytology , Superior Colliculi/physiology , Thalamus/cytology , Thalamus/physiology
6.
Nature ; 566(7744): 339-343, 2019 02.
Article in English | MEDLINE | ID: mdl-30760920

ABSTRACT

A psychotherapeutic regimen that uses alternating bilateral sensory stimulation (ABS) has been used to treat post-traumatic stress disorder. However, the neural basis that underlies the long-lasting effect of this treatment-described as eye movement desensitization and reprocessing-has not been identified. Here we describe a neuronal pathway driven by the superior colliculus (SC) that mediates persistent attenuation of fear. We successfully induced a lasting reduction in fear in mice by pairing visual ABS with conditioned stimuli during fear extinction. Among the types of visual stimulation tested, ABS provided the strongest fear-reducing effect and yielded sustained increases in the activities of the SC and mediodorsal thalamus (MD). Optogenetic manipulation revealed that the SC-MD circuit was necessary and sufficient to prevent the return of fear. ABS suppressed the activity of fear-encoding cells and stabilized inhibitory neurotransmission in the basolateral amygdala through a feedforward inhibitory circuit from the MD. Together, these results reveal the neural circuit that underlies an effective strategy for sustainably attenuating traumatic memories.


Subject(s)
Anxiety/psychology , Anxiety/therapy , Extinction, Psychological/physiology , Fear/physiology , Fear/psychology , Neural Pathways/physiology , Superior Colliculi/cytology , Superior Colliculi/physiology , Animals , Anxiety/physiopathology , Basolateral Nuclear Complex/cytology , Basolateral Nuclear Complex/physiology , Conditioning, Classical/physiology , Feedback, Physiological , Male , Mediodorsal Thalamic Nucleus/cytology , Mediodorsal Thalamic Nucleus/physiology , Mice , Neural Inhibition , Optogenetics , Photic Stimulation , Stress Disorders, Post-Traumatic , Time Factors
7.
Nat Commun ; 8: 14263, 2017 01 24.
Article in English | MEDLINE | ID: mdl-28117340

ABSTRACT

Models of visual attention postulate the existence of a saliency map whose function is to guide attention and gaze to the most conspicuous regions in a visual scene. Although cortical representations of saliency have been reported, there is mounting evidence for a subcortical saliency mechanism, which pre-dates the evolution of neocortex. Here, we conduct a strong test of the saliency hypothesis by comparing the output of a well-established computational saliency model with the activation of neurons in the primate superior colliculus (SC), a midbrain structure associated with attention and gaze, while monkeys watched video of natural scenes. We find that the activity of SC superficial visual-layer neurons (SCs), specifically, is well-predicted by the model. This saliency representation is unlikely to be inherited from fronto-parietal cortices, which do not project to SCs, but may be computed in SCs and relayed to other areas via tectothalamic pathways.


Subject(s)
Attention/physiology , Models, Neurological , Neurons/physiology , Superior Colliculi/physiology , Visual Perception/physiology , Animals , Computer Simulation , Macaca mulatta , Male , Models, Animal , Neural Pathways , Photic Stimulation/methods , Saccades , Software , Superior Colliculi/cytology , Thalamus/physiology
8.
Brain Res ; 1615: 106-115, 2015 Jul 30.
Article in English | MEDLINE | ID: mdl-25916576

ABSTRACT

Retinocollicular connections form precise topographical maps that are normally completed through the selective elimination of misplaced axons and the stabilization of topographically ordered axon terminals during early development. Omega-3 fatty acids, acquired exclusively through the diet, and its main metabolite, docosahexaenoic acid (DHA), are involved in brain development and synaptic maturation. We have previously shown that the nutritional restriction of omega-3/DHA results in abnormal retinocollicular topographical fine-tuning. Therefore, we studied the role of omega-3 fatty acids nutritional supplementation and the developmental time windows during which this postnatal supplementation would restore normal topographical maps in the visual system. Female rats and their litters were chronically fed with either control (soy oil) or restricted omega-3 (coconut oil) diets. Fish oil supplementation was introduced between either postnatal day (PND) 7-13, PND7-28 or PND21-42. At PND13, PND28 or PND42, animals received an anterograde eye injection of a neuronal tracer to visualize retinocollicular axons. Confirming previous observations we found that an omega-3/DHA deficiency resulted in an abnormally high innervation density of retinal axons at the visual layers of the superior colliculus (SC). Although a short-term fish oil supplementation between PND7-13 could not restore normal retinocollicular topography, an extended treatment between PND7-28 completely recovered normal innervation densities of retinotectal axons. However, a late onset supplementation protocol, between PND28-42, was no longer effective in the restoration of the abnormal topographical pattern induced by an early omega-3 nutritional malnutrition. The results suggest a critical period for omega3/DHA dietary intake for the proper development of visual topographical maps.


Subject(s)
Fatty Acids, Omega-3/administration & dosage , Retina/growth & development , Superior Colliculi/growth & development , Visual Pathways/growth & development , Animals , Dietary Supplements , Docosahexaenoic Acids/administration & dosage , Female , Rats , Retina/cytology , Superior Colliculi/cytology , Time Factors
9.
J Neurosci ; 35(15): 6079-92, 2015 Apr 15.
Article in English | MEDLINE | ID: mdl-25878281

ABSTRACT

Docosahexaenoic acid (DHA, 22:6n-3) is an essential component of the nervous system, and maternal n-3 polyunsaturated fatty acids (PUFAs) are an important source for brain development. Here, the impact of DHA on developing central neurons was examined using an accessible in vivo model. Xenopus laevis embryos from adult female frogs fed n-3 PUFA-adequate or deficient diets were analyzed every 10 weeks for up to 60 weeks, when frogs were then switched to a fish oil-supplemented diet. Lipid analysis showed that DHA was significantly reduced both in oocytes and tadpoles 40 weeks after deprivation, and brain DHA was reduced by 57% at 60 weeks. In vivo imaging of single optic tectal neurons coexpressing tdTomato and PSD-95-GFP revealed that neurons were morphologically simpler in tadpoles from frogs fed the deficient diet compared with the adequate diet. Tectal neurons had significantly fewer dendrite branches and shorter dendritic arbor over a 48 h imaging period. Postsynaptic cluster number and density were lower in neurons deprived of n-3 PUFA. Moreover, changes in neuronal morphology correlated with a 40% decrease in the levels of BDNF mRNA and mature protein in the brain, but not in TrkB. Importantly, switching to a fish oil-supplemented diet induced a recovery in DHA content in the frog embryos within 20 weeks and diminished the deprivation effects observed on tectal neurons of Stage 45 tadpoles. Consequently, our results indicate that DHA impacts dendrite maturation and synaptic connectivity in the developing brain, and it may be involved in neurotrophic support by BDNF.


Subject(s)
Central Nervous System/cytology , Central Nervous System/growth & development , Dendrites/pathology , Fatty Acids, Omega-3/metabolism , Gene Expression Regulation, Developmental/physiology , Neural Pathways/anatomy & histology , Neurons/cytology , Animals , Anura , Brain-Derived Neurotrophic Factor/genetics , Brain-Derived Neurotrophic Factor/metabolism , Dendrites/drug effects , Disks Large Homolog 4 Protein , Docosahexaenoic Acids/pharmacology , Dose-Response Relationship, Drug , Female , Green Fluorescent Proteins/genetics , Green Fluorescent Proteins/metabolism , Intracellular Signaling Peptides and Proteins/genetics , Intracellular Signaling Peptides and Proteins/metabolism , Lipids/analysis , Membrane Proteins/genetics , Membrane Proteins/metabolism , Neurogenesis , Neurons/drug effects , Pregnancy , Superior Colliculi/cytology , Time Factors , Xenopus laevis
10.
Nat Commun ; 6: 6756, 2015 Apr 09.
Article in English | MEDLINE | ID: mdl-25854147

ABSTRACT

The ability of animals to respond to life-threatening stimuli is essential for survival. Although vision provides one of the major sensory inputs for detecting threats across animal species, the circuitry underlying defensive responses to visual stimuli remains poorly defined. Here, we investigate the circuitry underlying innate defensive behaviours elicited by predator-like visual stimuli in mice. Our results demonstrate that neurons in the superior colliculus (SC) are essential for a variety of acute and persistent defensive responses to overhead looming stimuli. Optogenetic mapping revealed that SC projections to the lateral posterior nucleus (LP) of the thalamus, a non-canonical polymodal sensory relay, are sufficient to mimic visually evoked fear responses. In vivo electrophysiology experiments identified a di-synaptic circuit from SC through LP to the lateral amygdale (Amg), and lesions of the Amg blocked the full range of visually evoked defensive responses. Our results reveal a novel collicular-thalamic-Amg circuit important for innate defensive responses to visual threats.


Subject(s)
Amygdala/physiology , Fear/physiology , Instinct , Lateral Thalamic Nuclei/physiology , Neurons/physiology , Superior Colliculi/physiology , Visual Pathways/physiology , Visual Perception/physiology , Animals , Evoked Potentials, Visual , Lateral Thalamic Nuclei/cytology , Male , Mice , Mice, Inbred C57BL , Neural Pathways , Optogenetics , Photic Stimulation , Superior Colliculi/cytology , Thalamus/cytology , Thalamus/physiology
11.
Zoolog Sci ; 31(11): 748-57, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25366158

ABSTRACT

Parvalbumin (PV) is thought to play a major role in buffering intracellular calcium. We studied the distribution, morphology of PV-immunoreactive (IR) cells, and the effect of enucleation on the PV distribution in the superior colliculus (SC) in dog (Canis familiaris) and compared PV labeling to that of calbindin D28K (CB) and GABA. These cells formed three laminar tiers in the dog SC; 1) the upper superficial gray layer (SGL), 2) the lower optic layer (OL) and the upper intermediate gray layer, and 3) the deep layer. The third tier was not very distinct when compared with the other two tiers. The distribution of PV-IR cells is thus complementary to that of CB-IR tiers. Our present data on the distribution of PV-IR cells within the superficial layers are strikingly different from those in previously studied mammals, which show PV-IR cells within the lower SGL and upper OL. However, there were no distinct differences in distribution within the deep layers compared with that of previously studied mammals. PV-IR cells in the SC varied dramatically in morphology and size, and included round/oval, vertical fusiform, stellate, horizontal and pyriform cells. Two-color immunofluorescence revealed quantitatively that 11.67% of the PV-IR cells colocalized with GABA. Monocular enucleation appeared to have no effect on the distribution of PV-IR cells in the contralateral SC. Similar to CB, these data suggest that retinal projection may not control the expression of PV in the dog SC. These results provide important information for delineating similarities and differences in the neurochemical architecture of the visual system.


Subject(s)
Dogs/physiology , Eye Enucleation/veterinary , Parvalbumins/metabolism , Superior Colliculi/cytology , gamma-Aminobutyric Acid/metabolism , Animals , Neurons/metabolism , Neurons/ultrastructure , Superior Colliculi/physiology
12.
Neuroscience ; 256: 147-62, 2014 Jan 03.
Article in English | MEDLINE | ID: mdl-24183964

ABSTRACT

Multisensory integration has been widely studied in neurons of the mammalian superior colliculus (SC). This has led to the description of various determinants of multisensory integration, including those based on stimulus- and neuron-specific factors. The most widely characterized of these illustrate the importance of the spatial and temporal relationships of the paired stimuli as well as their relative effectiveness in eliciting a response in determining the final integrated output. Although these stimulus-specific factors have generally been considered in isolation (i.e., manipulating stimulus location while holding all other factors constant), they have an intrinsic interdependency that has yet to be fully elucidated. For example, changes in stimulus location will likely also impact both the temporal profile of response and the effectiveness of the stimulus. The importance of better describing this interdependency is further reinforced by the fact that SC neurons have large receptive fields, and that responses at different locations within these receptive fields are far from equivalent. To address these issues, the current study was designed to examine the interdependency between the stimulus factors of space and effectiveness in dictating the multisensory responses of SC neurons. The results show that neuronal responsiveness changes dramatically with changes in stimulus location - highlighting a marked heterogeneity in the spatial receptive fields of SC neurons. More importantly, this receptive field heterogeneity played a major role in the integrative product exhibited by stimulus pairings, such that pairings at weakly responsive locations of the receptive fields resulted in the largest multisensory interactions. Together these results provide greater insight into the interrelationship of the factors underlying multisensory integration in SC neurons, and may have important mechanistic implications for multisensory integration and the role it plays in shaping SC-mediated behaviors.


Subject(s)
Attention/physiology , Auditory Perception/physiology , Neurons/physiology , Space Perception/physiology , Superior Colliculi/cytology , Acoustic Stimulation , Action Potentials/physiology , Analysis of Variance , Animals , Brain Mapping , Cats , Photic Stimulation , Superior Colliculi/physiology
13.
Hear Res ; 300: 33-45, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23500650

ABSTRACT

The superior colliculus (SC) is critical for directing accurate head and eye movements to visual and acoustic targets. In visual cortex, areas involved in orienting of the head and eyes to a visual stimulus have direct projections to the SC. In auditory cortex of the cat, four areas have been identified to be critical for the accurate orienting of the head and body to an acoustic stimulus. These areas include primary auditory cortex (A1), the posterior auditory field (PAF), the dorsal zone of auditory cortex (DZ), and the auditory field of the anterior ectosylvian sulcus (fAES). Therefore, we hypothesized that these four regions of auditory cortex would have direct projections to the SC. To test this hypothesis, deposits of wheat germ agglutinin conjugated to horseradish peroxidase (WGA-HRP) were made into the superficial and deep layers of the SC to label, by means of retrograde transport, the auditory cortical origins of the corticotectal pathway. Bilateral examination of auditory cortex revealed that the vast majority of the labeled cells were located in the hemisphere ipsilateral to the SC injection. In ipsilateral auditory cortex, nearly all the labeled neurons were found in the infragranular layers, predominately in layer V. The largest population of labeled cells was located in the fAES. Few labeled neurons were identified in A1, PAF, or DZ. Thus, in contrast to the visual system, only one of the auditory cortical areas involved in orienting to an acoustic stimulus has a strong direct projection to the SC. Sound localization signals processed in primary (A1) and other non-primary (PAF and DZ) auditory cortices may be transmitted to the SC via a multi-synaptic corticotectal network.


Subject(s)
Auditory Cortex/physiology , Auditory Pathways/physiology , Neurons/physiology , Sound Localization , Superior Colliculi/physiology , Acoustic Stimulation , Animals , Auditory Cortex/cytology , Auditory Pathways/cytology , Cats , Eye Movements , Female , Head Movements , Neuroanatomical Tract-Tracing Techniques , Superior Colliculi/cytology , Synaptic Transmission
14.
J Comp Neurol ; 521(11): 2454-85, 2013 Aug 01.
Article in English | MEDLINE | ID: mdl-23296683

ABSTRACT

Polypteriform fishes are believed to be basal to other living ray-finned bony fishes, and they may be useful for providing information of the neural organization that existed in the brain of the earliest ray-finned fishes. The calcium-binding proteins calretinin (CR) and calbindin-D28k (CB) have been widely used to characterize neuronal populations in vertebrate brains. Here, the distribution of the immunoreactivity against CR and CB was investigated in the olfactory organ and brain of Polypterus senegalus and compared to the distribution of these molecules in other ray-finned fishes. In general, CB-immunoreactive (ir) neurons were less abundant than CR-ir cells. CR immunohistochemistry revealed segregation of CR-ir olfactory receptor neurons in the olfactory mucosa and their bulbar projections. Our results confirmed important differences between pallial regions in terms of CR immunoreactivity of cell populations and afferent fibers. In the habenula, these calcium-binding proteins revealed right-left asymmetry of habenular subpopulations and segregation of their interpeduncular projections. CR immunohistochemistry distinguished among some thalamic, pretectal, and posterior tubercle-derived populations. Abundant CR-ir populations were observed in the midbrain, including the tectum. CR immunoreactivity was also useful for characterizing a putative secondary gustatory/visceral nucleus in the isthmus, and for distinguishing territories in the primary viscerosensory column and octavolateral region. Comparison of the data obtained within a segmental neuromeric context indicates that some CB-ir and CR-ir populations in polypteriform fishes are shared with other ray-finned fishes, but other positive structures appear to have evolved following the separation between polypterids and other ray-finned fishes.


Subject(s)
Calbindin 2/metabolism , Calbindins/metabolism , Skates, Fish/physiology , Animals , Antibody Specificity , Brain Chemistry , Fluorescent Antibody Technique , Immunohistochemistry , Mesencephalon/chemistry , Mesencephalon/metabolism , Neurons/metabolism , Neurons/physiology , Olfactory Bulb/metabolism , Olfactory Mucosa/cytology , Olfactory Mucosa/innervation , Olfactory Mucosa/physiology , Olfactory Nerve/cytology , Olfactory Nerve/physiology , Olfactory Receptor Neurons/metabolism , Rhombencephalon/cytology , Rhombencephalon/metabolism , Superior Colliculi/cytology , Superior Colliculi/physiology , Suprachiasmatic Nucleus/cytology , Suprachiasmatic Nucleus/physiology , Thalamus/cytology , Thalamus/physiology
15.
Eur J Neurosci ; 36(11): 3459-70, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22934985

ABSTRACT

In amphibians, the midbrain tectum is regarded as the visual centre for object recognition but the functional role of forebrain centres in visual information processing is less clear. In order to address this question, the dorsal thalamus was lesioned in the salamander Plethodon shermani, and the effects on orienting behaviour or on visual processing in the tectum were investigated. In a two-alternative-choice task, the average number of orienting responses toward one of two competing prey or simple configural stimuli was significantly decreased in lesioned animals compared to that of controls and sham-lesioned animals. When stimuli were presented during recording from tectal neurons, the number of spikes on presentation of a stimulus in the excitatory receptive field and a second salient stimulus in the surround was significantly reduced in controls and sham-lesioned salamanders compared to single presentation of the stimulus in the excitatory receptive field, while this inhibitory effect on the number of spikes of tectal neurons was absent in thalamus-lesioned animals. In amphibians, the dorsal thalamus is part of the second visual pathway which extends from the tectum via the thalamus to the telencephalon. A feedback loop to the tectum is assumed to modulate visual processing in the tectum and to ensure orienting behaviour toward visual objects. It is concluded that the tectum-thalamus-telencephalon pathway contributes to the recognition and evaluation of objects and enables spatial attention in object selection. This attentional system in amphibians resembles that found in mammals and illustrates the essential role of attention for goal-directed visuomotor action.


Subject(s)
Attention , Pattern Recognition, Visual , Thalamus/physiology , Visual Pathways/physiology , Animals , Feedback, Physiological , Neurons/physiology , Orientation , Superior Colliculi/cytology , Superior Colliculi/physiology , Telencephalon/physiology , Urodela , Visual Fields
16.
J Neurosci ; 31(49): 17811-20, 2011 Dec 07.
Article in English | MEDLINE | ID: mdl-22159097

ABSTRACT

Habituation is the most basic form of learning, yet many gaps remain in our understanding of its underlying neural mechanisms. We demonstrate that in the owl's optic tectum (OT), a single, low-level, relatively short auditory stimulus is sufficient to induce a significant reduction in the neural response to a stimulus presented up to 60 s later. This type of neural adaptation was absent in neurons from the central nucleus of the inferior colliculus and from the auditory thalamus; however, it was apparent in the OT and the forebrain entopallium. By presenting sequences that alternate between two different auditory stimuli, we show that this long-lasting adaptation is stimulus specific. The response to an odd stimulus in the sequence was not smaller than the response to the same stimulus when it was first in the sequence. Finally, we measured the habituation of reflexive eye movements and show that the behavioral habituation is correlated with the neural adaptation. The finding of a long-lasting specific adaptation in areas related to the gaze control system and not elsewhere suggests its involvement in habituation processes and opens new directions for research on mechanisms of habituation.


Subject(s)
Adaptation, Physiological/physiology , Habituation, Psychophysiologic/physiology , Neurons/physiology , Acoustic Stimulation , Action Potentials/physiology , Animals , Behavior, Animal , Eye Movements/physiology , Female , Male , Orientation , Psychoacoustics , Sound Spectrography , Strigiformes , Superior Colliculi/cytology , Time Factors
17.
J Neurophysiol ; 106(6): 3091-101, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21957224

ABSTRACT

In environments containing sensory events at competing locations, selecting a target for orienting requires prioritization of stimulus values. Although the superior colliculus (SC) is causally linked to the stimulus selection process, the manner in which SC multisensory integration operates in a competitive stimulus environment is unknown. Here we examined how the activity of visual-auditory SC neurons is affected by placement of a competing target in the opposite hemifield, a stimulus configuration that would, in principle, promote interhemispheric competition for access to downstream motor circuitry. Competitive interactions between the targets were evident in how they altered unisensory and multisensory responses of individual neurons. Responses elicited by a cross-modal stimulus (multisensory responses) proved to be substantially more resistant to competitor-induced depression than were unisensory responses (evoked by the component modality-specific stimuli). Similarly, when a cross-modal stimulus served as the competitor, it exerted considerably more depression than did its individual component stimuli, in some cases producing more depression than predicted by their linear sum. These findings suggest that multisensory integration can help resolve competition among multiple targets by enhancing orientation to the location of cross-modal events while simultaneously suppressing orientation to events at alternate locations.


Subject(s)
Auditory Perception/physiology , Neural Inhibition/physiology , Neurons/physiology , Superior Colliculi/cytology , Superior Colliculi/physiology , Visual Perception/physiology , Acoustic Stimulation , Action Potentials/physiology , Animals , Cats , Models, Biological , Photic Stimulation , Psychophysics
18.
Restor Neurol Neurosci ; 28(2): 259-70, 2010.
Article in English | MEDLINE | ID: mdl-20404413

ABSTRACT

PURPOSE: Previous work has established that the integrative capacity of multisensory neurons in the superior colliculus (SC) matures over a protracted period of postnatal life (Wallace and Stein, 1997), and that the development of normal patterns of multisensory integration depends critically on early sensory experience (Wallace et al., 2004). Although these studies demonstrated the importance of early sensory experience in the creation of mature multisensory circuits, it remains unknown whether the reestablishment of sensory experience in adulthood can reverse these effects and restore integrative capacity. METHODS: The current study tested this hypothesis in cats that were reared in absolute darkness until adulthood and then returned to a normal housing environment for an equivalent period of time. Single unit extracellular recordings targeted multisensory neurons in the deep layers of the SC, and analyses were focused on both conventional measures of multisensory integration and on more recently developed methods designed to characterize spatiotemporal receptive fields (STRF). RESULTS: Analysis of the STRF structure and integrative capacity of multisensory SC neurons revealed significant modifications in the temporal response dynamics of multisensory responses (e.g., discharge durations, peak firing rates, and mean firing rates), as well as significant changes in rates of spontaneous activation and degrees of multisensory integration. CONCLUSIONS: These results emphasize the importance of early sensory experience in the establishment of normal multisensory processing architecture and highlight the limited plastic potential of adult multisensory circuits.


Subject(s)
Neuronal Plasticity/physiology , Neurons/physiology , Sensory Deprivation/physiology , Superior Colliculi/cytology , Visual Fields/physiology , Visual Perception/physiology , Acoustic Stimulation/methods , Action Potentials/physiology , Animals , Auditory Perception/physiology , Brain Mapping , Cats , Photic Stimulation/methods
19.
J Neurophysiol ; 101(5): 2380-94, 2009 May.
Article in English | MEDLINE | ID: mdl-19261710

ABSTRACT

Temporal and spatial correlations between auditory and visual stimuli facilitate the perception of unitary events and improve behavioral responses. However, it is not clear how combined visual and auditory information is processed in single neurons. Here we studied responses of multisensory neurons in the barn owl's optic tectum (the avian homologue of the superior colliculus) to visual, auditory, and bimodal stimuli. We specifically focused on responses to sequences of repeated stimuli. We first report that bimodal stimulation tends to elicit more spikes than in the responses to its unimodal components (a phenomenon known as multisensory enhancement). However, this tendency was found to be history-dependent; multisensory enhancement was mostly apparent in the first stimulus of the sequence and to a much lesser extent in the subsequent stimuli. Next, a vector-strength analysis was applied to quantify the phase locking of the responses to the stimuli. We report that in a substantial number of multisensory neurons responses to sequences of bimodal stimuli elicited spike trains that were better phase locked to the stimulus than spike trains elicited by stimulating with the unimodal counterparts (visual or auditory). We conclude that multisensory enhancement can be manifested in better phase locking to the stimulus as well as in more spikes.


Subject(s)
Action Potentials/physiology , Sensory Receptor Cells/physiology , Strigiformes/anatomy & histology , Superior Colliculi/cytology , Superior Colliculi/physiology , Acoustic Stimulation/methods , Animals , Auditory Perception , Models, Biological , Photic Stimulation/methods , Psychophysics , Reaction Time , Strigiformes/physiology , Time Factors , Visual Perception
20.
Neural Netw ; 22(7): 913-21, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19084371

ABSTRACT

To localize a seen object, the superior colliculus of the barn owl integrates the visual and auditory localization cues which are accessed from the sensory system of the brain. These cues are formed as visual and auditory maps. The alignment between visual and auditory maps is very important for accurate localization in prey behavior. Blindness or prism wearing may interfere this alignment. The juvenile barn owl could adapt its auditory map to this mismatch after several weeks training. Here we investigate this process by building a computational model of auditory and visual integration in deep Superior Colliculus (SC). The adaptation of the map alignment is based on activity dependent axon developing in Inferior Colliculus (IC). This axon growing process is instructed by an inhibitory network in SC while the strength of the inhibition is adjusted by Spike Timing Dependent Plasticity (STDP). The simulation results of this model are in line with the biological experiment and support the idea that STDP is involved in the alignment of sensory maps. This model also provides a new spiking neuron based mechanism capable of eliminating the disparity in visual and auditory map integration.


Subject(s)
Action Potentials/physiology , Adaptation, Physiological/physiology , Models, Neurological , Neuronal Plasticity/physiology , Sensory Receptor Cells/physiology , Superior Colliculi/cytology , Acoustic Stimulation/methods , Afferent Pathways/physiology , Animals , Brain Mapping , Neural Inhibition/physiology , Photic Stimulation/methods , Sound Localization/physiology , Space Perception/physiology , Strigiformes/anatomy & histology , Strigiformes/physiology
SELECTION OF CITATIONS
SEARCH DETAIL