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1.
Neuropsychopharmacology ; 49(6): 993-1006, 2024 May.
Article in English | MEDLINE | ID: mdl-38233571

ABSTRACT

The medial prefrontal cortex (mPFC) is critical to cognitive and emotional function and underlies many neuropsychiatric disorders, including mood, fear and anxiety disorders. In rodents, disruption of mPFC activity affects anxiety- and depression-like behavior, with specialized contributions from its subdivisions. The rodent mPFC is divided into the dorsomedial prefrontal cortex (dmPFC), spanning the anterior cingulate cortex (ACC) and dorsal prelimbic cortex (PL), and the ventromedial prefrontal cortex (vmPFC), which includes the ventral PL, infralimbic cortex (IL), and in some studies the dorsal peduncular cortex (DP) and dorsal tenia tecta (DTT). The DP/DTT have recently been implicated in the regulation of stress-induced sympathetic responses via projections to the hypothalamus. While many studies implicate the PL and IL in anxiety-, depression-like and fear behavior, the contribution of the DP/DTT to affective and emotional behavior remains unknown. Here, we used chemogenetics and optogenetics to bidirectionally modulate DP/DTT activity and examine its effects on affective behaviors, fear and stress responses in C57BL/6J mice. Acute chemogenetic activation of DP/DTT significantly increased anxiety-like behavior in the open field and elevated plus maze tests, as well as passive coping in the tail suspension test. DP/DTT activation also led to an increase in serum corticosterone levels and facilitated auditory fear extinction learning and retrieval. Activation of DP/DTT projections to the dorsomedial hypothalamus (DMH) acutely decreased freezing at baseline and during extinction learning, but did not alter affective behavior. These findings point to the DP/DTT as a new regulator of affective behavior and fear extinction in mice.


Subject(s)
Affect , Behavior, Animal , Extinction, Psychological , Fear , Prefrontal Cortex , Female , Male , Mice , Affect/physiology , Anxiety/physiopathology , Behavior, Animal/physiology , Coping Skills , Corticosterone/blood , Extinction, Psychological/physiology , Fear/physiology , Fear/psychology , Freezing Reaction, Cataleptic , Hindlimb Suspension , Maze Learning , Mice, Inbred C57BL , Neural Pathways , Prefrontal Cortex/cytology , Prefrontal Cortex/physiology , Sound , Swimming , Tectum Mesencephali/cytology , Tectum Mesencephali/physiology
2.
Neuron ; 109(5): 805-822.e6, 2021 03 03.
Article in English | MEDLINE | ID: mdl-33357384

ABSTRACT

When navigating the environment, animals need to prioritize responses to the most relevant stimuli. Although a theoretical framework for selective visual attention exists, its circuit implementation has remained obscure. Here we investigated how larval zebrafish select between simultaneously presented visual stimuli. We found that a mix of winner-take-all (WTA) and averaging strategies best simulates behavioral responses. We identified two circuits whose activity patterns predict the relative saliencies of competing visual objects. Stimuli presented to only one eye are selected by WTA computation in the inner retina. Binocularly presented stimuli, on the other hand, are processed by reciprocal, bilateral connections between the nucleus isthmi (NI) and the tectum. This interhemispheric computation leads to WTA or averaging responses. Optogenetic stimulation and laser ablation of NI neurons disrupt stimulus selection and behavioral action selection. Thus, depending on the relative locations of competing stimuli, a combination of retinotectal and isthmotectal circuits enables selective visual attention.


Subject(s)
Attention/physiology , Visual Pathways/physiology , Visual Perception/physiology , Animals , Behavior, Animal , Models, Neurological , Optogenetics , Photic Stimulation , Retina/physiology , Tectum Mesencephali/physiology , Zebrafish
3.
Science ; 370(6512): 46, 2020 Oct 02.
Article in English | MEDLINE | ID: mdl-33004508
4.
Sci Rep ; 10(1): 16220, 2020 10 01.
Article in English | MEDLINE | ID: mdl-33004866

ABSTRACT

The parabigeminal nucleus (PBG) is the mammalian homologue to the isthmic complex of other vertebrates. Optogenetic stimulation of the PBG induces freezing and escape in mice, a result thought to be caused by a PBG projection to the central nucleus of the amygdala. However, the isthmic complex, including the PBG, has been classically considered satellite nuclei of the Superior Colliculus (SC), which upon stimulation of its medial part also triggers fear and avoidance reactions. As the PBG-SC connectivity is not well characterized, we investigated whether the topology of the PBG projection to the SC could be related to the behavioral consequences of PBG stimulation. To that end, we performed immunohistochemistry, in situ hybridization and neural tracer injections in the SC and PBG in a diurnal rodent, the Octodon degus. We found that all PBG neurons expressed both glutamatergic and cholinergic markers and were distributed in clearly defined anterior (aPBG) and posterior (pPBG) subdivisions. The pPBG is connected reciprocally and topographically to the ipsilateral SC, whereas the aPBG receives afferent axons from the ipsilateral SC and projected exclusively to the contralateral SC. This contralateral projection forms a dense field of terminals that is restricted to the medial SC, in correspondence with the SC representation of the aerial binocular field which, we also found, in O. degus prompted escape reactions upon looming stimulation. Therefore, this specialized topography allows binocular interactions in the SC region controlling responses to aerial predators, suggesting a link between the mechanisms by which the SC and PBG produce defensive behaviors.


Subject(s)
Behavior, Animal/physiology , Escape Reaction/physiology , Fear/physiology , Neural Pathways/physiology , Octodon/physiology , Superior Colliculi/physiology , Tectum Mesencephali/physiology , Animals , Brain Mapping , Female , Male , Optogenetics
5.
J Neurophysiol ; 124(6): 1968-1985, 2020 12 01.
Article in English | MEDLINE | ID: mdl-33085555

ABSTRACT

Superior colliculus (SC) is a midbrain structure that integrates sensory inputs and generates motor commands to initiate innate motor behaviors. Its retinorecipient superficial layers (sSC) receive dense cholinergic projections from the parabigeminal nucleus (PBN). Our previous in vitro study revealed that acetylcholine induces fast inward current followed by prominent GABAergic inhibition within the sSC circuits (Endo T, Yanagawa Y, Obata K, Isa T. J Neurophysiol 94: 3893-3902, 2005). Acetylcholine-mediated facilitation of GABAergic inhibition may play an important role in visual signal processing in the sSC; however, both the anatomical and physiological properties of cholinergic inputs from PBN have not been studied in detail in vivo. In this study, we specifically visualized and optogenetically manipulated the cholinergic neurons in the PBN after focal injections of Cre-dependent viral vectors in mice that express Cre in cholinergic neurons. We revealed that the cholinergic projections terminated densely in the medial part of the mouse sSC. This suggests that the cholinergic inputs mediate visual processing in the upper visual field, which would be critical for predator detection. We further analyzed the physiological roles of the cholinergic inputs by recording looming-evoked visual responses from sSC neurons during optogenetic activation or inactivation of PBN cholinergic neurons in anesthetized mice. We found that optogenetic manipulations in either direction induced response suppression in most neurons, whereas response facilitation was observed in a few neurons after the optogenetic activation. These results support a circuit model that suggests that the PBN cholinergic inputs enhance functions of the sSC in detecting visual targets by facilitating the center excitation-surround inhibition.NEW & NOTEWORTHY The modulatory role of the cholinergic inputs from the parabigeminal nucleus in the visual responses in the superficial superior colliculus (sSC) remains unknown. Here we report that the cholinergic projections terminate densely in the medial sSC and optogenetic manipulations of the cholinergic inputs affect the looming-evoked response and enhance surround inhibition in the sSC. Our data suggest that cholinergic inputs to the sSC contribute to the visual detection of predators.


Subject(s)
Cholinergic Neurons/physiology , Evoked Potentials, Visual/physiology , Tectum Mesencephali/physiology , Visual Fields/physiology , Visual Pathways/physiology , Animals , Male , Mice , Mice, Transgenic , Optogenetics , Superior Colliculi/physiology
6.
Brain Res ; 1747: 147068, 2020 11 15.
Article in English | MEDLINE | ID: mdl-32827547

ABSTRACT

The emergence of visual saliency has been widely studied in the primary visual cortex and the superior colliculus (SC) in mammals. There are fewer studies on the pop-out response to motion direction contrasting stimuli taken in the optic tectum (OT, homologous to mammalian SC), and these are mainly of owls and fish. To our knowledge the influence of spatial luminance has not been reported. In this study, we have recorded multi-units in pigeon OT and analyzed the tectal response to spatial luminance contrasting, motion direction contrasting, and contrasting stimuli from both feature dimensions. The comparison results showed that 1) the tectal response would pop-out in either motion direction or spatial luminance contrasting conditions. 2) The modulation from motion direction contrasting was independent of the temporal luminance variation of the visual stimuli. 3) When both spatial luminance and motion direction were salient, the response of tectal neurons was modulated more intensely by motion direction than by spatial luminance. The phenomenon was consistent with the innate instinct of avians in their natural environment. This study will help to deepen the understanding of mechanisms involved in bottom-up visual information processing and selective attention in the avian.


Subject(s)
Motion Perception/physiology , Neurons/physiology , Tectum Mesencephali/physiology , Visual Pathways/physiology , Visual Perception/physiology , Animals , Columbidae , Photic Stimulation , Vision, Ocular/physiology
7.
J Comp Neurol ; 528(8): 1423-1435, 2020 06.
Article in English | MEDLINE | ID: mdl-31749169

ABSTRACT

Responses of ON- and OFF-ganglion cells (GCs) were recorded extracellularly from their axon terminals in the medial sublamina of tectal retino-recipient layer of immobilized cyprinid fish (goldfish and carp). These units were recorded deeper than direction selective (DS) ones and at the same depth where responses of orientation selective (OS) GCs were recorded. Prominent responses of these units are evoked by small contrast spots flickering within or moving across their visual field. They are not selective either to the direction of motion or to the orientation of stimuli and are not characterized by any spontaneous spike activity. We refer to these fish GCs as spot detectors (SDs) by analogy with the frog SD. Receptive fields (RFs) of SDs are organized concentrically: the excitatory center (about 4.5°) is surrounded by opponent periphery. Study of interactions in the RF has shown that inhibitory influences are generated already inside the central RF area. This fact suggests that RFs of SDs cannot be defined as homogeneous sensory zone driven by a linear mechanism of response generation. Physiological properties of fish SDs are compared with the properties of frog SDs and analogous mammalian retinal GCs-local edge detectors (LEDs). The potential role of the SDs in visually guided fish behavior is discussed.


Subject(s)
Photic Stimulation/methods , Retina/physiology , Tectum Mesencephali/physiology , Visual Fields/physiology , Visual Pathways/physiology , Animals , Anura , Carps , Goldfish , Mammals , Retina/chemistry , Species Specificity , Tectum Mesencephali/chemistry , Visual Pathways/chemistry
8.
Curr Biol ; 29(11): 1771-1786.e5, 2019 06 03.
Article in English | MEDLINE | ID: mdl-31104935

ABSTRACT

Animals must frequently perform a sequence of behaviors to achieve a specific goal. However, the neural mechanisms that promote the continuation and completion of such action sequences are not well understood. Here, we characterize the anatomy, physiology, and function of the nucleus isthmi (NI), a cholinergic nucleus thought to modulate tectal-dependent, goal-directed behaviors. We find that the larval zebrafish NI establishes reciprocal connectivity with the optic tectum and identify two distinct types of isthmic projection neuron that either connect ipsilaterally to retinorecipient laminae of the tectum and pretectum or bilaterally to both tectal hemispheres. Laser ablation of NI caused highly specific deficits in tectally mediated loom-avoidance and prey-catching behavior. In the context of hunting, NI ablation did not affect prey detection or hunting initiation but resulted in larvae failing to sustain prey-tracking sequences and aborting their hunting routines. Moreover, calcium imaging revealed elevated neural activity in NI following onset of hunting behavior. We propose a model in which NI provides state-dependent feedback facilitation to the optic tectum and pretectum to potentiate neural activity and increase the probability of consecutive prey-tracking maneuvers during hunting sequences.


Subject(s)
Efferent Pathways/physiology , Goldfish/physiology , Tectum Mesencephali/physiology , Visual Pathways/physiology , Zebrafish/physiology , Animals , Goldfish/anatomy & histology , Neurons/cytology , Superior Colliculi/anatomy & histology , Superior Colliculi/physiology , Tectum Mesencephali/anatomy & histology , Zebrafish/anatomy & histology
9.
Sci Rep ; 9(1): 4420, 2019 03 14.
Article in English | MEDLINE | ID: mdl-30872640

ABSTRACT

How diverse adult stem and progenitor populations regenerate tissue following damage to the brain is poorly understood. In highly regenerative vertebrates, such as zebrafish, radial-glia (RG) and neuro-epithelial-like (NE) stem/progenitor cells contribute to neuronal repair after injury. However, not all RG act as neural stem/progenitor cells during homeostasis in the zebrafish brain, questioning the role of quiescent RG (qRG) post-injury. To understand the function of qRG during regeneration, we performed a stab lesion in the adult midbrain tectum to target a population of homeostatic qRG, and investigated their proliferative behaviour, differentiation potential, and Wnt/ß-catenin signalling. EdU-labelling showed a small number of proliferating qRG after injury (pRG) but that progeny are restricted to RG. However, injury promoted proliferation of NE progenitors in the internal tectal marginal zone (TMZi) resulting in amplified regenerative neurogenesis. Increased Wnt/ß-catenin signalling was detected in TMZi after injury whereas homeostatic levels of Wnt/ß-catenin signalling persisted in qRG/pRG. Attenuation of Wnt signalling suggested that the proliferative response post-injury was Wnt/ß-catenin-independent. Our results demonstrate that qRG in the tectum have restricted capability in neuronal repair, highlighting that RG have diverse functions in the zebrafish brain. Furthermore, these findings suggest that endogenous stem cell compartments compensate lost tissue by amplifying homeostatic growth.


Subject(s)
Neural Stem Cells/cytology , Neurogenesis , Neuroglia/cytology , Neurons/cytology , Superior Colliculi/cytology , Tectum Mesencephali/cytology , Animals , Animals, Genetically Modified , Cell Proliferation , Neural Stem Cells/physiology , Neuroglia/physiology , Neurons/physiology , Superior Colliculi/physiology , Tectum Mesencephali/physiology , Wnt Signaling Pathway , Zebrafish , Zebrafish Proteins/metabolism
10.
Neurosci Lett ; 698: 39-43, 2019 04 17.
Article in English | MEDLINE | ID: mdl-30615974

ABSTRACT

In mammals, the brain decreases in mass and volume as a function of age. The current study is, to the best of our knowledge, the first to investigate age-related changes in brain mass and volume in birds. Following perfusion, brains from young and old homing pigeons were weighed on a balance and orthogonal measurements of the telencephalon, cerebellum, and tecta were obtained with a digital caliper. It was found that older pigeons had heavier brains than younger pigeons, a difference that remained after controlling for body mass. Additionally, older pigeons had on average greater estimated telencephalon volumes than younger pigeons, again also after controlling for body mass. Cerebellum and right tectum volumes also differed between age groups after controlling for body mass, with older pigeons having a larger cerebellum and right tectum than younger pigeons. In sum, brains are on average heavier and larger in old pigeons, which display age-related cognitive decline, compared to young adult pigeons. The larger brain in older homing pigeons also lies in stark contrast with aging of the mammalian brain.


Subject(s)
Aging/physiology , Brain/anatomy & histology , Columbidae/physiology , Animals , Cerebellum/anatomy & histology , Cerebellum/physiology , Columbidae/anatomy & histology , Homing Behavior , Organ Size , Tectum Mesencephali/anatomy & histology , Tectum Mesencephali/physiology , Telencephalon/anatomy & histology , Telencephalon/physiology
11.
Brain Res ; 1708: 20-26, 2019 04 01.
Article in English | MEDLINE | ID: mdl-30527677

ABSTRACT

Responses of direction selective (DS) units of retinal and tectal origin were recorded extracellularly from the tectum opticum (TO) of immobilized fish. The data were collected from three cyprinid species - goldfish, carp and roach. Responses of the retinal DS ganglion cells (GCs) were recorded from their axon terminals in the superficial layers of TO. According to their preferred directions DS GCs, characterized by small receptive fields (3-8°), can be divided in three distinct groups, each group containing ON and OFF subtypes approximately in equal quantity. Conversely, direction-selective tectal neurons (DS TNs), recorded at two different tectal levels deeper than the zone of retinal DS afferents, are characterized by large receptive fields (up to 60°) and are indifferent to any sign of contrast i.e. can be considered as ON-OFF type units. Fish DS TNs unlike the retinal DS GCs, select four preferred directions. Three types of tectal DS units prefer practically the same directions as those already selected on the retinal level - caudo-rostral, dorso-ventral and ventro-dorsal. The fact that three preferred directions of DS GCs and DS TNs coincide allows us to assume that three types of DS GCs are input neurons for corresponding types of DS TNs. The fourth group of DS TNs has the emergent rostro-caudal preference not explicitly present in any of the DS GC inputs. These units are recorded in deep TO layers exclusively. Receptive fields of these DS neurons could be entirely formed on the tectal level. Possible interrelations between retinal and tectal DS units are discussed.


Subject(s)
Orientation/physiology , Retinal Ganglion Cells/physiology , Superior Colliculi/physiology , Action Potentials/physiology , Animals , Carps , Cyprinidae , Goldfish , Photic Stimulation , Retina/physiology , Retinal Ganglion Cells/metabolism , Spatial Behavior/physiology , Superior Colliculi/metabolism , Tectum Mesencephali/physiology , Visual Pathways/physiology
12.
J Neurophysiol ; 119(5): 1947-1961, 2018 05 01.
Article in English | MEDLINE | ID: mdl-29442555

ABSTRACT

The circuit controlling visually guided behavior in nonmammalian vertebrates, such as Xenopus tadpoles, includes retinal projections to the contralateral optic tectum, where visual information is processed, and tectal motor outputs projecting ipsilaterally to hindbrain and spinal cord. Tadpoles have an intertectal commissure whose function is unknown, but it might transfer information between the tectal lobes. Differences in visual experience between the two eyes have profound effects on the development and function of visual circuits in animals with binocular vision, but the effects on animals with fully crossed retinal projections are not clear. We tested the effect of monocular visual experience on the visuomotor circuit in Xenopus tadpoles. We show that cutting the intertectal commissure or providing visual experience to one eye (monocular visual experience) is sufficient to disrupt tectally mediated visual avoidance behavior. Monocular visual experience induces asymmetry in tectal circuit activity across the midline. Repeated exposure to monocular visual experience drives maturation of the stimulated retinotectal synapses, seen as increased AMPA-to-NMDA ratios, induces synaptic plasticity in intertectal synaptic connections, and induces bilaterally asymmetric changes in the tectal excitation-to-inhibition ratio (E/I). We show that unilateral expression of peptides that interfere with AMPA or GABAA receptor trafficking alters E/I in the transfected tectum and is sufficient to degrade visuomotor behavior. Our study demonstrates that monocular visual experience in animals with fully crossed visual systems produces asymmetric circuit function across the midline and degrades visuomotor behavior. The data further suggest that intertectal inputs are an integral component of a bilateral visuomotor circuit critical for behavior. NEW & NOTEWORTHY The developing optic tectum of Xenopus tadpoles represents a unique circuit in which laterally positioned eyes provide sensory input to a circuit that is transiently monocular, but which will be binocular in the animal's adulthood. We challenge the idea that the two lobes of tadpole optic tectum function independently by testing the requirement of interhemispheric communication and demonstrate that unbalanced sensory input can induce structural and functional plasticity in the tectum sufficient to disrupt function.


Subject(s)
Behavior, Animal/physiology , Neuronal Plasticity/physiology , Psychomotor Performance/physiology , Retina/physiology , Tectum Mesencephali/physiology , Vision, Binocular/physiology , Vision, Monocular/physiology , Visual Pathways/physiology , Xenopus laevis/physiology , Animals , Larva/physiology , Superior Colliculi/physiology
13.
Eur J Neurosci ; 44(11): 2899-2908, 2016 12.
Article in English | MEDLINE | ID: mdl-27717088

ABSTRACT

Projections from the posterior intralaminar thalamic nuclei and the superior colliculus (SC) to the subthalamic nucleus (STN) and the zona incerta (ZI) have been described in the primate and rodent. The aims of this study was to investigate several questions on these projections, using modern neurotracing techniques in rats, to advance our understanding of the role of STN and ZI. We examined whether projection patterns to the subthlamus can be used to identify homologues of the primate centromedian (CM) and the parafascicular nucleus (Pf) in the rodent, the topography of the projection including what percent of intralaminar neurons participate in the projections, and electron microscopic examination of intralaminar synaptic boutons in STN. The aim on the SC-subthalamic projection was to examine whether STN is the main target of the projection. This study revealed: (i) the areas similar to primate CM and Pf could be recognized in the rat; (ii) the Pf-like area sends a very heavy topographically organized projection to STN but very sparse projection to ZI, which suggested that Pf might control basal ganglia function through STN; (iii) the projection from the CM-like area to the subthalamus was very sparse; (iv) Pf boutons and randomly sampled asymmetrical synapses had similar distributions on the dendrites of STN neurons; and (v) the lateral part of the deep layers of SC sends a very heavy projection to ZI and moderate to sparse projection to limited parts of STN, suggesting that SC is involved in a limited control of basal ganglia function.


Subject(s)
Subthalamic Nucleus/physiology , Tectum Mesencephali/physiology , Zona Incerta/physiology , Animals , Male , Neural Pathways , Neurons/cytology , Neurons/physiology , Rats , Rats, Sprague-Dawley , Subthalamic Nucleus/cytology , Synapses/physiology , Tectum Mesencephali/cytology , Zona Incerta/cytology
14.
Neurosci Lett ; 629: 137-142, 2016 08 26.
Article in English | MEDLINE | ID: mdl-27394688

ABSTRACT

Acetylcholine receptors contribute to the control of neuronal and neuronal network activity from insects to humans. We have investigated the action of acetylcholine receptors in the optic tectum of Rana temporaria (common frog). Our previous studies have demonstrated that acetylcholine activates presynaptic nicotinic receptors, when released into the frog optic tectum as a co-mediator during firing of a single retinal ganglion cell, and causes: a) potentiation of retinotectal synaptic transmission, and b) facilitation of transition of the tectum column to a higher level of activity. In the present study we have shown that endogenous acetylcholine also activates muscarinic receptors, leading to a delayed inhibition of recurrent excitatory synaptic transmission in the tectum column. The delay of muscarinic inhibition was evaluated to be of ∼80ms, with an extent of inhibition of ∼2 times. The inhibition of the recurrent excitation determines transition of the tectum column back to its resting state, giving a functional sense for the inhibition.


Subject(s)
Acetylcholine/physiology , Receptors, Muscarinic/physiology , Retinal Ganglion Cells/physiology , Synaptic Transmission , Tectum Mesencephali/physiology , Animals , Atropine/administration & dosage , Electric Stimulation , Models, Neurological , Muscarinic Antagonists/administration & dosage , Neural Inhibition , Rana temporaria
15.
J Neurosci ; 36(16): 4470-81, 2016 Apr 20.
Article in English | MEDLINE | ID: mdl-27098691

ABSTRACT

Accurate localization of sound sources is essential for survival behavior in many species. The inferior colliculi (ICs) are the first point in the auditory pathway where cues used to locate sounds, ie, interaural time differences (ITDs), interaural level differences (ILDs), and pinna spectral cues, are all represented in the same location. These cues are first extracted separately on each side of the midline in brainstem nuclei that project to the ICs. Because of this segregation, each IC predominantly represents stimuli in the contralateral hemifield. We tested the hypothesis that commissural connections between the ICs mediate gain control that enhances sound localization acuity. We recorded IC neurons sensitive to either ITDs or ILDs in anesthetized guinea pig, before, during, and following recovery from deactivation of the contralateral IC by cryoloop cooling or microdialysis of procaine. During deactivation, responses were rescaled by divisive gain change and additive shifts, which reduced the dynamic range of ITD and ILD response functions and the ability of neurons to signal changes in sound location. These data suggest that each IC exerts multiplicative gain control and subtractive shifts over the other IC that enhances the neural representation of sound location. Furthermore, this gain control operates in a similar manner on both ITD- and ILD-sensitive neurons, suggesting a shared mechanism operates across localization cues. Our findings reveal a novel dependence of sound localization on commissural processing. SIGNIFICANCE STATEMENT: Sound localization, a fundamental process in hearing, is dependent on bilateral computations in the brainstem. How this information is transmitted from the brainstem to the auditory cortex, through several stages of processing, without loss of signal fidelity, is not clear. We show that the ability of neurons in the auditory midbrain to encode azimuthal sound location is dependent on gain control mediated by the commissure of the inferior colliculi. This finding demonstrates that commissural processing between homologous auditory nuclei, on either side of the midline, enhances the precision of sound localization.


Subject(s)
Acoustic Stimulation/methods , Auditory Pathways/physiology , Mesencephalon/physiology , Sound Localization/physiology , Tectum Mesencephali/physiology , Action Potentials/physiology , Animals , Female , Guinea Pigs , Male
16.
J Comp Neurol ; 524(14): 2886-913, 2016 10 01.
Article in English | MEDLINE | ID: mdl-26991544

ABSTRACT

Previous studies have demonstrated that the optic tecta of the left and right brain halves reciprocally inhibit each other in birds. In mammals, the superior colliculus receives inhibitory γ-aminobutyric acid (GABA)ergic input from the basal ganglia via both the ipsilateral and the contralateral substantia nigra pars reticulata (SNr). This contralateral SNr projection is important in intertectal inhibition. Because the basal ganglia are evolutionarily conserved, the tectal projections of the SNr may show a similar pattern in birds. Therefore, the SNr could be a relay station in an indirect tecto-tectal pathway constituting the neuronal substrate for the tecto-tectal inhibition. To test this hypothesis, we performed bilateral anterograde and retrograde tectal tracing combined with GABA immunohistochemistry in pigeons. Suprisingly, the SNr has only ipsilateral projections to the optic tectum, and these are non-GABAergic. Inhibitory GABAergic input to the contralateral optic tectum arises instead from a nearby tegmental region that receives input from the ipsilateral optic tectum. Thus, a disynaptic pathway exists that possibly constitutes the anatomical substrate for the inhibitory tecto-tectal interaction. This pathway likely plays an important role in attentional switches between the laterally placed eyes of birds. J. Comp. Neurol. 524:2886-2913, 2016. © 2016 Wiley Periodicals, Inc.


Subject(s)
GABAergic Neurons/physiology , Superior Colliculi/physiology , Tectum Mesencephali/physiology , Tegmentum Mesencephali/physiology , Visual Pathways/physiology , Animals , Columbidae , Female , GABAergic Neurons/chemistry , Male , Superior Colliculi/chemistry , Tectum Mesencephali/chemistry , Tegmentum Mesencephali/chemistry , Visual Pathways/chemistry
17.
J Comp Neurol ; 524(5): 963-85, 2016 Apr 01.
Article in English | MEDLINE | ID: mdl-26287809

ABSTRACT

Birds are almost always said to have two visual pathways from the retina to the telencephalon: thalamofugal terminating in the Wulst, and tectofugal terminating in the entopallium. Often ignored is a second tectofugal pathway that terminates in the nidopallium medial to and separate from the entopallium (e.g., Gamlin and Cohen [1986] J Comp Neurol 250:296-310). Using standard tract-tracing and electroanatomical techniques, we extend earlier evidence of a second tectofugal pathway in songbirds (Wild [1994] J Comp Neurol 349:512-535), by showing that visual projections to nucleus uvaeformis (Uva) of the posterior thalamus in zebra finches extend farther rostrally than to Uva, as generally recognized in the context of the song control system. Projections to "rUva" resulted from injections of biotinylated dextran amine into the lateral pontine nucleus (PL), and led to extensive retrograde labeling of tectal neurons, predominantly in layer 13. Injections in rUva also resulted in extensive retrograde labeling of predominantly layer 13 tectal neurons, retrograde labeling of PL neurons, and anterograde labeling of PL. It thus appears that some tectal neurons could project to rUva and PL via branched axons. Ascending projections of rUva terminated throughout a visually responsive region of the intermediate nidopallium (NI) lying between the nucleus interface medially and the entopallium laterally. Lastly, as shown by Clarke in pigeons ([1977] J Comp Neurol 174:535-552), we found that PL projects to caudal cerebellar folia.


Subject(s)
Finches/physiology , Pontine Tegmentum/physiology , Posterior Thalamic Nuclei/physiology , Tectum Mesencephali/physiology , Acoustic Stimulation/methods , Animals , Female , Finches/anatomy & histology , Male , Photic Stimulation/methods , Pontine Tegmentum/cytology , Posterior Thalamic Nuclei/cytology , Songbirds , Tectum Mesencephali/cytology , Visual Pathways/cytology
18.
Synapse ; 69(6): 299-313, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25727065

ABSTRACT

The neuropsychopharmacological basis of fear- or panic-related behavior has been the focus of several studies. Some mesencephalic tectum (MT) structures, such as the superior colliculus (SC) and dorsal periaqueductal gray matter (dPAG), are considered to be responsible for the control of defensive responses evoked during threatening situations. Furthermore, the pars reticulata of the substantia nigra (SNpr) sends inputs to the SC that can work as a sensory channel to MT neurons fundamental for the elaboration of defensive responses. The purpose of the present study was to investigate the role of striato-nigral GABAergic inputs in the activity of nigro-tectal outputs during the elaboration of defensive behavior using a GABA(A) receptor selective blockade in the MT of mice confronted pre-treated with Bothrops alternatus. Mice with injections of physiological saline into the SNpr and treated with a GABA(A) receptor selective antagonist in the MT displayed an increase in panic-related behavior, expressed by an increase in the duration of freezing, frequency of nonoriented escape and frequency of total escape responses during the confrontation with the snake. However, intra-SNpr injections of cobalt chloride followed by MT injections of bicuculline caused a significant decrease in the duration of freezing and total escape responses. In addition, intra-SNpr injections of lidocaine followed by MT injections of bicuculline caused an increase in panic-related behavior. The results highlight the involvement of SNpr and MT structures in the organization of defensive behaviors and suggest an inhibitory control of striatonigral-nigrotectal pathways during the elaboration of fear- and panic-related behavior.


Subject(s)
Corpus Striatum/physiology , Escape Reaction/physiology , Panic/physiology , Substantia Nigra/physiology , Tectum Mesencephali/physiology , gamma-Aminobutyric Acid/metabolism , Animals , Bothrops , Corpus Striatum/drug effects , Escape Reaction/drug effects , Freezing Reaction, Cataleptic/drug effects , Freezing Reaction, Cataleptic/physiology , GABA-A Receptor Antagonists/pharmacology , Male , Mice, Inbred C57BL , Neural Inhibition/drug effects , Neural Inhibition/physiology , Neural Pathways/drug effects , Neural Pathways/physiology , Panic/drug effects , Receptors, GABA-A/metabolism , Spatial Behavior/drug effects , Spatial Behavior/physiology , Substantia Nigra/drug effects , Tectum Mesencephali/drug effects
19.
Neural Plast ; 2015: 819257, 2015.
Article in English | MEDLINE | ID: mdl-25789177

ABSTRACT

Juvenile barn owls readily adapt to prismatic spectacles, whereas adult owls living under standard aviary conditions do not. We previously demonstrated that phosphorylation of the cyclic-AMP response element-binding protein (CREB) provides a readout of the instructive signals that guide plasticity in juveniles. Here we investigated phosphorylation of calcium/calmodulin-dependent protein kinase II (pCaMKII) in both juveniles and adults. In contrast to CREB, we found no differences in pCaMKII expression between prism-wearing and control juveniles within the external nucleus of the inferior colliculus (ICX), the major site of plasticity. For prism-wearing adults that hunted live mice and are capable of adaptation, expression of pCaMKII was increased relative to prism-wearing adults that fed passively on dead mice and are not capable of adaptation. This effect did not bear the hallmarks of instructive information: it was not localized to rostral ICX and did not exhibit a patchy distribution reflecting discrete bimodal stimuli. These data are consistent with a role for CaMKII as a permissive rather than an instructive factor. In addition, the paucity of pCaMKII expression in passively fed adults suggests that the permissive default setting is "off" in adults.


Subject(s)
Adaptation, Physiological , Calcium-Calmodulin-Dependent Protein Kinase Type 2/metabolism , Neuronal Plasticity , Predatory Behavior/physiology , Tectum Mesencephali/physiology , Age Factors , Animals , Phosphorylation , Sound Localization/physiology , Space Perception/physiology , Strigiformes , Tectum Mesencephali/metabolism
20.
J Integr Neurosci ; 14(1): 31-52, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25553912

ABSTRACT

Sensitivity to the sign of contrast of direction-selective (DS) and orientation-selective (OS) ganglion cells (GCs) was investigated with selective stimulation of different chromatic types of cones. It was shown that the DS GCs that were classified with the use of achromatic stimuli as belonging to the ON type responded to selective stimulation of the long-wave cones as the ON type also, while the stimulation of middle-wave or short-wave cones elicited the OFF type responses. Character of the responses of DS GCs of the OFF type was exactly the opposite. OS GCs, which responded to achromatic stimuli as the ON-OFF type, responded to selective stimulation of the long-wave cones as the ON-OFF type as well, responded to middle-wave stimulation as the OFF type and to stimulation of short-wave cones it responded mainly as the ON type. At the same time, under color-selective stimulation, both DS and OS GCs retained the directional and orientation selectivity with the same preferred directions. The results obtained are in favor of the idea that the signals from the different chromatic types of cones are combined in the outer synaptic layer of the retina at the inputs of bipolar cells using sign-inverting and/or sign-conserving synapses, while specific spatial properties of motion detectors are formed in the inner synaptic layer.


Subject(s)
Color Vision/physiology , Motion Perception/physiology , Retinal Cone Photoreceptor Cells/physiology , Tectum Mesencephali/physiology , Visual Pathways/physiology , Action Potentials/physiology , Animals , Biophysics , Color Perception/physiology , Goldfish , Orientation , Photic Stimulation , Retina/cytology , Signal Detection, Psychological
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