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1.
Neuroscience ; 496: 230-240, 2022 08 01.
Article in English | MEDLINE | ID: mdl-35724770

ABSTRACT

Animals perceive threat information mainly from vision, and the subcortical visual pathway plays a critical role in the rapid processing of fear visual information. The superior colliculus (SC) and lateral posterior (LP) nuclei of the thalamus are key components of the subcortical visual pathway; however, how animals encode and transmit fear visual information is unclear. To evaluate the response characteristics of neurons in SC and LP thalamic nuclei under fear visual stimuli, extracellular action potentials (spikes) and local field potential (LFP) signals were recorded under looming and dimming visual stimuli. The results showed that both SC and LP thalamic nuclei were strongly responsive to looming visual stimuli but not sensitive to dimming visual stimuli. Under the looming visual stimulus, the theta (θ) frequency bands of both nuclei showed obvious oscillations, which markedly enhanced the synchronization between neurons. The functional network characteristics also indicated that the network connection density and information transmission efficiency were higher under fear visual stimuli. These findings suggest that both SC and LP thalamic nuclei can effectively identify threatening fear visual information and rapidly transmit it between nuclei through the θ frequency band. This discovery can provide a basis for subsequent coding and decoding studies in the subcortical visual pathways.


Subject(s)
Posterior Thalamic Nuclei , Superior Colliculi , Animals , Fear/physiology , Lateral Thalamic Nuclei/physiology , Mice , Posterior Thalamic Nuclei/physiology , Superior Colliculi/physiology , Thalamic Nuclei/physiology , Visual Pathways/physiology
2.
Neuron ; 109(12): 1996-2008.e6, 2021 06 16.
Article in English | MEDLINE | ID: mdl-33979633

ABSTRACT

Sensory processing involves information flow between neocortical areas, assumed to rely on direct intracortical projections. However, cortical areas may also communicate indirectly via higher-order nuclei in the thalamus, such as the pulvinar or lateral posterior nucleus (LP) in the visual system of rodents. The fine-scale organization and function of these cortico-thalamo-cortical pathways remains unclear. We find that responses of mouse LP neurons projecting to higher visual areas likely derive from feedforward input from primary visual cortex (V1) combined with information from many cortical and subcortical areas, including superior colliculus. Signals from LP projections to different higher visual areas are tuned to specific features of visual stimuli and their locomotor context, distinct from the signals carried by direct intracortical projections from V1. Thus, visual transthalamic pathways are functionally specific to their cortical target, different from feedforward cortical pathways, and combine information from multiple brain regions, linking sensory signals with behavioral context.


Subject(s)
Lateral Thalamic Nuclei/physiology , Neurons/physiology , Pulvinar/physiology , Thalamus/physiology , Visual Cortex/physiology , Visual Pathways/physiology , Animals , Cerebral Cortex/physiology , Locomotion/physiology , Mice , Photic Stimulation , Superior Colliculi/physiology
3.
Neuron ; 106(1): 21-36, 2020 04 08.
Article in English | MEDLINE | ID: mdl-32272065

ABSTRACT

Since the discovery of ocular dominance plasticity, neuroscientists have understood that changes in visual experience during a discrete developmental time, the critical period, trigger robust changes in the visual cortex. State-of-the-art tools used to probe connectivity with cell-type-specific resolution have expanded the understanding of circuit changes underlying experience-dependent plasticity. Here, we review the visual circuitry of the mouse, describing projections from retina to thalamus, between thalamus and cortex, and within cortex. We discuss how visual circuit development leads to precise connectivity and identify synaptic loci, which can be altered by activity or experience. Plasticity extends to visual features beyond ocular dominance, involving subcortical and cortical regions, and connections between cortical inhibitory interneurons. Experience-dependent plasticity contributes to the alignment of networks spanning retina to thalamus to cortex. Disruption of this plasticity may underlie aberrant sensory processing in some neurodevelopmental disorders.


Subject(s)
Dominance, Ocular/physiology , Neuronal Plasticity/physiology , Retina/physiology , Thalamus/physiology , Visual Cortex/physiology , Animals , Critical Period, Psychological , Geniculate Bodies/growth & development , Geniculate Bodies/physiology , Lateral Thalamic Nuclei/growth & development , Lateral Thalamic Nuclei/physiology , Mice , Neurodevelopmental Disorders/physiopathology , Retina/growth & development , Superior Colliculi/growth & development , Superior Colliculi/physiology , Suprachiasmatic Nucleus/growth & development , Suprachiasmatic Nucleus/physiology , Synapses/physiology , Thalamus/growth & development , Vision, Binocular/physiology , Visual Cortex/growth & development , Visual Pathways/growth & development , Visual Pathways/physiology
4.
World Neurosurg ; 137: 310-318, 2020 05.
Article in English | MEDLINE | ID: mdl-32036065

ABSTRACT

The thalamus is a deep cerebral structure that is crucial for proper neurological functioning as it transmits signals from nearly all pathways in the body. Insult to the thalamus can, therefore, result in complex syndromes involving sensation, cognition, executive function, fine motor control, emotion, and arousal, to name a few. Specific territories in the thalamus that are supplied by deep cerebral arteries have been shown to correlate with clinical symptoms. The aim of this review is to enhance our understanding of the arterial anatomy of the thalamus and the complications that can arise from lesions to it by considering the functions of known thalamic nuclei supplied by each vascular territory.


Subject(s)
Basilar Artery/anatomy & histology , Brain Infarction/physiopathology , Circle of Willis/anatomy & histology , Posterior Cerebral Artery/anatomy & histology , Thalamus/blood supply , Anterior Thalamic Nuclei/anatomy & histology , Anterior Thalamic Nuclei/blood supply , Anterior Thalamic Nuclei/physiology , Geniculate Bodies/anatomy & histology , Geniculate Bodies/blood supply , Geniculate Bodies/physiology , Humans , Lateral Thalamic Nuclei/anatomy & histology , Lateral Thalamic Nuclei/blood supply , Lateral Thalamic Nuclei/physiology , Mediodorsal Thalamic Nucleus/anatomy & histology , Mediodorsal Thalamic Nucleus/blood supply , Mediodorsal Thalamic Nucleus/physiology , Pulvinar/anatomy & histology , Pulvinar/blood supply , Pulvinar/physiology , Thalamus/anatomy & histology , Thalamus/physiology , Ventral Thalamic Nuclei/anatomy & histology , Ventral Thalamic Nuclei/blood supply , Ventral Thalamic Nuclei/physiology
5.
J Comp Neurol ; 528(11): 1917-1941, 2020 07 15.
Article in English | MEDLINE | ID: mdl-31983057

ABSTRACT

Cross-modal auditory influence on cell activity in the primary visual cortex emerging at short latencies raises the possibility that the first-order visual thalamic nucleus, which is considered dedicated to unimodal visual processing, could contribute to cross-modal sensory processing, as has been indicated in the auditory and somatosensory systems. To test this hypothesis, the effects of sound stimulation on visual cell activity in the dorsal lateral geniculate nucleus were examined in anesthetized rats, using juxta-cellular recording and labeling techniques. Visual responses evoked by light (white LED) were modulated by sound (noise burst) given simultaneously or 50-400 ms after the light, even though sound stimuli alone did not evoke cell activity. Alterations of visual response were observed in 71% of cells (57/80) with regard to response magnitude, latency, and/or burst spiking. Suppression predominated in response magnitude modulation, but de novo responses were also induced by combined stimulation. Sound affected not only onset responses but also late responses. Late responses were modulated by sound given before or after onset responses. Further, visual responses evoked by the second light stimulation of a double flash with a 150-700 ms interval were also modulated by sound given together with the first light stimulation. In morphological analysis of labeled cells projection cells comparable to X-, Y-, and W-like cells and interneurons were all susceptible to auditory influence. These findings suggest that the first-order visual thalamic nucleus incorporates auditory influence into parallel and complex thalamic visual processing for cross-modal modulation of visual attention and perception.


Subject(s)
Auditory Perception/physiology , Lateral Thalamic Nuclei/physiology , Neurons/physiology , Visual Perception/physiology , Acoustic Stimulation , Animals , Male , Photic Stimulation , Rats , Rats, Wistar
6.
J Comp Neurol ; 528(1): 95-107, 2020 01 01.
Article in English | MEDLINE | ID: mdl-31265129

ABSTRACT

Higher-order visual thalamus communicates broadly and bi-directionally with primary and extrastriate cortical areas in various mammals. In primates, the pulvinar is a topographically and functionally organized thalamic nucleus that is largely dedicated to visual processing. Still, a more granular connectivity map is needed to understand the role of thalamocortical loops in visually guided behavior. Similarly, the secondary visual thalamic nucleus in mice (the lateral posterior nucleus, LP) has extensive connections with cortex. To resolve the precise connectivity of these circuits, we first mapped mouse visual cortical areas using intrinsic signal optical imaging and then injected fluorescently tagged retrograde tracers (cholera toxin subunit B) into retinotopically-matched locations in various combinations of seven different visual areas. We find that LP neurons representing matched regions in visual space but projecting to different extrastriate areas are found in different topographically organized zones, with few double-labeled cells (~4-6%). In addition, V1 and extrastriate visual areas received input from the ventrolateral part of the laterodorsal nucleus of the thalamus (LDVL). These observations indicate that the thalamus provides topographically organized circuits to each mouse visual area and raise new questions about the contributions from LP and LDVL to cortical activity.


Subject(s)
Brain Mapping/methods , Lateral Thalamic Nuclei/physiology , Visual Cortex/physiology , Visual Pathways/physiology , Animals , Female , Lateral Thalamic Nuclei/chemistry , Male , Mice, Inbred C57BL , Visual Cortex/chemistry , Visual Pathways/chemistry
7.
Neuron ; 104(3): 588-600.e5, 2019 11 06.
Article in English | MEDLINE | ID: mdl-31623918

ABSTRACT

Whether mouse visual cortex contains orderly feature maps is debated. The overlapping pattern of geniculocortical inputs with M2 muscarinic acetylcholine receptor-rich patches in layer 1 (L1) suggests a non-random architecture. Here, we found that L1 inputs from the lateral posterior thalamus (LP) avoid patches and target interpatches. Channelrhodopsin-2-assisted mapping of excitatory postsynaptic currents (EPSCs) in L2/3 shows that the relative excitation of parvalbumin-expressing interneurons (PVs) and pyramidal neurons (PNs) by dLGN, LP, and cortical feedback is distinct and depends on whether the neurons reside in clusters aligned with patches or interpatches. Paired recordings from PVs and PNs show that unitary inhibitory postsynaptic currents (uIPSCs) are larger in interpatches than in patches. The spatial clustering of inhibition is matched by dense clustering of PV terminals in interpatches. The results show that the excitation/inhibition balance across V1 is organized into patch and interpatch subnetworks, which receive distinct long-range inputs and are specialized for the processing of distinct spatiotemporal features.


Subject(s)
Geniculate Bodies/physiology , Interneurons/physiology , Neural Inhibition/physiology , Pyramidal Cells/physiology , Visual Cortex/physiology , Animals , Brain Mapping , Excitatory Postsynaptic Potentials , Inhibitory Postsynaptic Potentials , Interneurons/metabolism , Lateral Thalamic Nuclei/physiology , Mice , Neural Pathways , Parvalbumins/metabolism
8.
Front Neural Circuits ; 13: 51, 2019.
Article in English | MEDLINE | ID: mdl-31447652

ABSTRACT

The cerebellar involvement in cognitive functions such as attention, language, working memory, emotion, goal-directed behavior and spatial navigation is constantly growing. However, an exact connectivity map between the hippocampus and cerebellum in mice is still unknown. Here, we conducted a tracing study to identify the sequence of transsynaptic, cerebellar-hippocampal connections in the mouse brain using combinations of Recombinant adeno-associated virus (rAAV) and pseudotyped deletion-mutant rabies (RABV) viruses. Stereotaxic injection of a primarily anterograde rAAV-WGA (wheat germ agglutinin)-Cre tracer virus in the deep cerebellar nuclei (DCN) of a Cre-dependent tdTomato reporter mouse resulted in strong tdTomato labeling in hippocampal CA1 neurons, retrosplenial cortex (RSC), rhinal cortex (RC) as well as thalamic and cerebellar areas. Whereas hippocampal injections with the retrograde tracer virus rAAV-TTC (tetanus toxin C fragment)-eGFP, displayed eGFP positive cells in the rhinal cortex and subiculum. To determine the sequence of mono-transsynaptic connections between the cerebellum and hippocampus, we used the retrograde tracer RABVΔG-eGFP(EnvA). The tracing revealed a direct connection from the dentate gyrus (DG) in the hippocampus to the RSC, RC and subiculum (S), which are monosynaptically connected to thalamic laterodorsal and ventrolateral areas. These thalamic nuclei are directly connected to cerebellar fastigial (FN), interposed (IntP) and lateral (Lat) nuclei, discovering a new projection route from the fastigial to the laterodorsal thalamic nucleus in the mouse brain. Collectively, our findings suggest a new cerebellar-hippocampal connection via the laterodorsal and ventrolateral thalamus to RSC, RC and S. These results strengthen the notion of the cerebellum's involvement in cognitive functions such as spatial navigation via a polysynaptic circuitry.


Subject(s)
Cerebellar Nuclei/physiology , Hippocampus/physiology , Lateral Thalamic Nuclei/physiology , Nerve Net/physiology , Thalamic Nuclei/physiology , Ventral Thalamic Nuclei/physiology , Animals , Cerebellar Nuclei/chemistry , Female , HEK293 Cells , Hippocampus/chemistry , Humans , Lateral Thalamic Nuclei/chemistry , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic , Nerve Net/chemistry , Thalamic Nuclei/chemistry , Ventral Thalamic Nuclei/chemistry
9.
FASEB J ; 33(6): 7018-7036, 2019 06.
Article in English | MEDLINE | ID: mdl-30857416

ABSTRACT

The pedunculopontine tegmental nucleus (PPT) and laterodorsal tegmental nucleus (LDT) are heterogeneous brainstem structures that contain cholinergic, glutamatergic, and GABAergic neurons. PPT/LDT neurons are suggested to modulate both cognitive and noncognitive functions, yet the extent to which acetylcholine (ACh) signaling from the PPT/LDT is necessary for normal behavior remains uncertain. We addressed this issue by using a mouse model in which PPT/LDT cholinergic signaling is highly decreased by selective deletion of the vesicular ACh transporter (VAChT) gene. This approach interferes exclusively with ACh signaling, leaving signaling by other neurotransmitters from PPT/LDT cholinergic neurons intact and sparing other cells. VAChT mutants were examined on different PPT/LDT-associated cognitive domains. Interestingly, VAChT mutants showed no attentional deficits and only minor cognitive flexibility impairments while presenting large deficiencies in both spatial and cued Morris water maze (MWM) tasks. Conversely, working spatial memory determined with the Y-maze and spatial memory measured with the Barnes maze were not affected, suggesting that deficits in MWM were unrelated to spatial memory abnormalities. Supporting this interpretation, VAChT mutants exhibited alterations in anxiety-like behavior and increased corticosterone levels after exposure to the MWM, suggesting altered stress response. Thus, PPT/LDT VAChT-mutant mice present little cognitive impairment per se, yet they exhibit increased susceptibility to stress, which may lead to performance deficits in more stressful conditions.-Janickova, H., Kljakic, O., Rosborough, K., Raulic, S., Matovic, S., Gros, R., Saksida, L. M., Bussey, T. J., Inoue, W., Prado, V. F., Prado, M. A. M. Selective decrease of cholinergic signaling from pedunculopontine and laterodorsal tegmental nuclei has little impact on cognition but markedly increases susceptibility to stress.


Subject(s)
Cognition/physiology , Lateral Thalamic Nuclei/physiology , Pedunculopontine Tegmental Nucleus/physiology , Stress, Physiological , Animals , Attention , Corticosterone/blood , Gene Expression Regulation , Vesicular Acetylcholine Transport Proteins/genetics
10.
Neural Plast ; 2018: 6109723, 2018.
Article in English | MEDLINE | ID: mdl-30534151

ABSTRACT

Mechanisms underlying remifentanil- (RF-) induced hyperalgesia, a phenomenon that is generally named as opioid-induced hyperalgesia (OIH), still remain elusive. The ventral posterior lateral nucleus (VPL) of the thalamus, a key relay station for the transmission of nociceptive information to the cerebral cortex, is activated by RF infusion. Electroacupuncture (EA) is an effective method for the treatment of pain. This study aimed to explore the role of VPL in the development of OIH and the effect of EA treatment on OIH in rats. RF was administered to rats via the tail vein for OIH induction. Paw withdrawal threshold (PWT) in response to mechanical stimuli and paw withdrawal latency (PWL) to thermal stimulation were tested in rats for the assessment of mechanical allodynia and thermal hyperalgesia, respectively. Spontaneous neuronal activity and local field potential (LFP) in VPL were recorded in freely moving rats using the in vivo multichannel recording technique. EA at 2 Hz frequency (pulse width 0.6 ms, 1-3 mA) was applied to the bilateral acupoints "Zusanli" (ST.36) and "Sanyinjiao" (SP.6) in rats. The results showed that both the PWT and PWL were significantly decreased after RF infusion to rats. Meanwhile, both the spontaneous neuronal firing rate and the theta band oscillation in VPL LFP were increased on day 3 post-RF infusion, indicating that the VPL may promote the development of RF-induced hyperalgesia by regulating the pain-related cortical activity. Moreover, 2 Hz-EA reversed the RF-induced decrease both in PWT and PWL of rats and also abrogated the RF-induced augmentation of the spontaneous neuronal activity and the power spectral density (PSD) of the theta band oscillation in VPL LFP. These results suggested that 2 Hz-EA attenuates the remifentanil-induced hyperalgesia via reducing the excitability of VPL neurons and the low-frequency (theta band) oscillation in VPL LFP.


Subject(s)
Electroacupuncture/methods , Hyperalgesia/chemically induced , Hyperalgesia/therapy , Lateral Thalamic Nuclei/physiology , Remifentanil/toxicity , Ventral Thalamic Nuclei/physiology , Analgesics, Opioid/toxicity , Animals , Hyperalgesia/physiopathology , Lateral Thalamic Nuclei/drug effects , Male , Pain/chemically induced , Pain/physiopathology , Pain Management/methods , Rats , Rats, Sprague-Dawley , Treatment Outcome , Ventral Thalamic Nuclei/drug effects
11.
Nat Commun ; 9(1): 1232, 2018 03 26.
Article in English | MEDLINE | ID: mdl-29581428

ABSTRACT

Animals respond to environmental threats, e.g. looming visual stimuli, with innate defensive behaviors such as escape and freezing. The key neural circuits that participate in the generation of such dimorphic defensive behaviors remain unclear. Here we show that the dimorphic behavioral patterns triggered by looming visual stimuli are mediated by parvalbumin-positive (PV+) projection neurons in mouse superior colliculus (SC). Two distinct groups of SC PV+ neurons form divergent pathways to transmit threat-relevant visual signals to neurons in the parabigeminal nucleus (PBGN) and lateral posterior thalamic nucleus (LPTN). Activations of PV+ SC-PBGN and SC-LPTN pathways mimic the dimorphic defensive behaviors. The PBGN and LPTN neurons are co-activated by looming visual stimuli. Bilateral inactivation of either nucleus results in the defensive behavior dominated by the other nucleus. Together, these data suggest that the SC orchestrates dimorphic defensive behaviors through two separate tectofugal pathways that may have interactions.


Subject(s)
Escape Reaction , Fear/physiology , Freezing Reaction, Cataleptic , Mesencephalon/physiology , Photic Stimulation , Superior Colliculi/physiology , Animals , Lateral Thalamic Nuclei/cytology , Lateral Thalamic Nuclei/physiology , Male , Mesencephalon/cytology , Mice , Mice, Inbred C57BL , Neurons/physiology , Superior Colliculi/cytology , Visual Pathways
12.
Vis Neurosci ; 34: E011, 2017 01.
Article in English | MEDLINE | ID: mdl-28965504

ABSTRACT

Comparative studies have greatly contributed to our understanding of the organization and function of visual pathways of the brain, including that of humans. This comparative approach is a particularly useful tactic for studying the pulvinar nucleus, an enigmatic structure which comprises the largest territory of the human thalamus. This review focuses on the regions of the mouse pulvinar that receive input from the superior colliculus, and highlights similarities of the tectorecipient pulvinar identified across species. Open questions are discussed, as well as the potential contributions of the mouse model for endeavors to elucidate the function of the pulvinar nucleus.


Subject(s)
Lateral Thalamic Nuclei/physiology , Pulvinar/physiology , Superior Colliculi/physiology , Visual Pathways/physiology , Animals , Mice
13.
Neuroscience ; 349: 128-143, 2017 05 04.
Article in English | MEDLINE | ID: mdl-28237814

ABSTRACT

Dense reciprocal connections link the rat anterior thalamic nuclei with the prelimbic, anterior cingulate and retrosplenial cortices, as well as with the subiculum and postsubiculum. The present study compared the ipsilateral thalamic-cortical connections with the corresponding crossed, contralateral connections between these same sets of regions. All efferents from the anteromedial thalamic nucleus to the cortex, as well as those to the subiculum, remained ipsilateral. In contrast, all of these target sites provided reciprocal, bilateral projections to the anteromedial nucleus. While the anteroventral thalamic nucleus often shared this same asymmetric pattern of cortical connections, it received relatively fewer crossed inputs than the anteromedial nucleus. This difference was most marked for the anterior cingulate projections, as those to the anteroventral nucleus remained almost entirely ipsilateral. Unlike the anteromedial nucleus, the anteroventral nucleus also appeared to provide a restricted, crossed projection to the contralateral retrosplenial cortex. Meanwhile, the closely related laterodorsal thalamic nucleus had almost exclusively ipsilateral efferent and afferent cortical connections. Likewise, within the hippocampus, the postsubiculum seemingly had only ipsilateral efferent and afferent connections with the anterior thalamic and laterodorsal nuclei. While the bilateral cortical projections to the anterior thalamic nuclei originated predominantly from layer VI, the accompanying sparse projections from layer V largely gave rise to ipsilateral thalamic inputs. In testing a potentially unifying principle of anterior thalamic - cortical interactions, a slightly more individual pattern emerged that reinforces other evidence of functional differences within the anterior thalamic and also helps to explain the consequences of unilateral interventions involving these nuclei.


Subject(s)
Cerebral Cortex/physiology , Hippocampus/physiology , Neural Pathways/physiology , Animals , Brain Mapping , Gyrus Cinguli/physiology , Lateral Thalamic Nuclei/physiology , Male , Rats , Thalamic Nuclei/physiology
14.
Neurobiol Learn Mem ; 133: 69-78, 2016 09.
Article in English | MEDLINE | ID: mdl-27266961

ABSTRACT

The anterior and lateral thalamus has long been considered to play an important role in spatial and mnemonic cognitive functions; however, it remains unclear whether each region makes a unique contribution to spatial information processing. We begin by reviewing evidence from anatomical studies and electrophysiological recordings which suggest that at least one of the functions of the anterior thalamus is to guide spatial orientation in relation to a global or distal spatial framework, while the lateral thalamus serves to guide behavior in relation to a local or proximal framework. We conclude by reviewing experimental work using targeted manipulations (lesion or neuronal silencing) of thalamic nuclei during spatial behavior and single-unit recordings from neuronal representations of space. Our summary of this literature suggests that although the evidence strongly supports a working model of spatial information processing involving the anterior thalamus, research regarding the role of the lateral thalamus is limited and requires further attention. We therefore identify a number of major gaps in this research and suggest avenues of future study that could potentially solidify our understanding of the relative roles of anterior and lateral thalamic regions in spatial representation and memory.


Subject(s)
Anterior Thalamic Nuclei/physiology , Lateral Thalamic Nuclei/physiology , Spatial Behavior/physiology , Spatial Memory/physiology , Animals , Anterior Thalamic Nuclei/cytology , Anterior Thalamic Nuclei/pathology , Humans , Lateral Thalamic Nuclei/cytology , Lateral Thalamic Nuclei/pathology
15.
J Physiol ; 594(7): 1911-29, 2016 Apr 01.
Article in English | MEDLINE | ID: mdl-26842995

ABSTRACT

KEY POINTS: The lateral posterior and posterior thalamic nuclei have been implicated in aspects of visually guided behaviour and reflex responses to light, including those dependent on melanopsin photoreception. Here we investigated the extent and basic properties of visually evoked activity across the mouse lateral posterior and posterior thalamus. We show that a subset of retinal projections to these regions derive from melanopsin-expressing retinal ganglion cells and find many cells that exhibit melanopsin-dependent changes in firing. We also show that subsets of cells across these regions integrate signals from both eyes in various ways and that, within the lateral posterior thalamus, visual responses are retinotopically ordered. ABSTRACT: In addition to the primary thalamocortical visual relay in the lateral geniculate nuclei, a number of other thalamic regions contribute to aspects of visual processing. Thus, the lateral posterior thalamic nuclei (LP/pulvinar) appear important for various functions including determining visual saliency, visually guided behaviours and, alongside dorsal portions of the posterior thalamic nuclei (Po), multisensory processing of information related to aversive stimuli. However, despite the growing importance of mice as a model for understanding visual system organisation, at present we know very little about the basic visual response properties of cells in the mouse LP or Po. Prompted by earlier suggestions that melanopsin photoreception might be important for certain functions of these nuclei, we first employ specific viral tracing to show that a subset of retinal projections to the LP derive from melanopsin-expressing retinal ganglion cells. We next use multielectrode electrophysiology to demonstrate that LP and dorsal Po cells exhibit a variety of responses to simple visual stimuli including two distinct classes that express melanopsin-dependent changes in firing (together comprising ∼25% of neurons we recorded). We also show that subgroups of LP/Po cells integrate signals from both eyes in various ways and that, within the LP, visual responses are retinotopically ordered. Together our data reveal a diverse population of visually responsive neurons across the LP and dorsal Po whose properties align with some of the established functions of these nuclei and suggest new possible routes through which melanopsin photoreception could contribute to reflex light responses and/or higher order visual processing.


Subject(s)
Evoked Potentials, Visual , Lateral Thalamic Nuclei/physiology , Posterior Thalamic Nuclei/physiology , Retinal Ganglion Cells/metabolism , Animals , Lateral Thalamic Nuclei/cytology , Mice , Mice, Inbred C57BL , Posterior Thalamic Nuclei/cytology , Retinal Ganglion Cells/physiology , Rod Opsins/genetics , Rod Opsins/metabolism , Visual Pathways/cytology , Visual Pathways/physiology
16.
J Neurophysiol ; 114(4): 2390-403, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26289469

ABSTRACT

The pulvinar is the largest extrageniculate thalamic visual nucleus in mammals. It establishes reciprocal connections with virtually all visual cortexes and likely plays a role in transthalamic cortico-cortical communication. In cats, the lateral posterior nucleus (LP) of the LP-pulvinar complex can be subdivided in two subregions, the lateral (LPl) and medial (LPm) parts, which receive a predominant input from the striate cortex and the superior colliculus, respectively. Here, we revisit the receptive field structure of LPl and LPm cells in anesthetized cats by determining their first-order spatiotemporal profiles through reverse correlation analysis following sparse noise stimulation. Our data reveal the existence of previously unidentified receptive field profiles in the LP nucleus both in space and time domains. While some cells responded to only one stimulus polarity, the majority of neurons had receptive fields comprised of bright and dark responsive subfields. For these neurons, dark subfields' size was larger than that of bright subfields. A variety of receptive field spatial organization types were identified, ranging from totally overlapped to segregated bright and dark subfields. In the time domain, a large spectrum of activity overlap was found, from cells with temporally coinciding subfield activity to neurons with distinct, time-dissociated subfield peak activity windows. We also found LP neurons with space-time inseparable receptive fields and neurons with multiple activity periods. Finally, a substantial degree of homology was found between LPl and LPm first-order receptive field spatiotemporal profiles, suggesting a high integration of cortical and subcortical inputs within the LP-pulvinar complex.


Subject(s)
Lateral Thalamic Nuclei/physiology , Neurons/physiology , Visual Perception/physiology , Animals , Cats , Microelectrodes , Photic Stimulation , Signal Processing, Computer-Assisted , Visual Pathways/physiology
17.
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
18.
J Manipulative Physiol Ther ; 37(5): 277-86, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24928636

ABSTRACT

OBJECTIVES: High-velocity low-amplitude spinal manipulation (HVLA-SM), as performed by doctors who use manual therapy (eg, doctors of chiropractic and osteopathy), results in mechanical hypoalgesia in clinical settings. This hypoalgesic effect has previously been attributed to alterations in peripheral and/or central pain processing. The objective of this study was to determine whether thrust magnitude of a simulated HVLA-SM alters mechanical trunk response thresholds in wide dynamic range (WDR) and/or nociceptive specific (NS) lateral thalamic neurons. METHODS: Extracellular recordings were carried out in the thalamus of 15 anesthetized Wistar rats. Lateral thalamic neurons having receptive fields, which included the lumbar dorsal-lateral trunk, were characterized as either WDR (n=22) or NS (n=25). Response thresholds to electronic von Frey (rigid tip) mechanical trunk stimuli were determined in 3 directions (dorsal-ventral, 45° caudalward, and 45° cranialward) before and immediately after the dorsal-ventral delivery of a 100-millisecond HVLA-SM at 3 thrust magnitudes (control, 55%, 85% body weight). RESULTS: There was a significant difference in mechanical threshold between 85% body weight manipulation and control thrust magnitudes in the dorsal-ventral direction in NS neurons (P=.01). No changes were found in WDR neurons at either HVLA-SM thrust magnitude. CONCLUSIONS: This study is the first to investigate the effect of HVLA-SM thrust magnitude on WDR and NS lateral thalamic mechanical response threshold. Our data suggest that, at the single lateral thalamic neuron level, there may be a minimal spinal manipulative thrust magnitude required to elicit an increase in trunk mechanical response thresholds.


Subject(s)
Lateral Thalamic Nuclei/physiology , Manipulation, Spinal/methods , Animals , Electrodes , Male , Neurons/physiology , Nociceptors/physiology , Rats, Wistar
19.
Curr Biol ; 24(6): 587-97, 2014 Mar 17.
Article in English | MEDLINE | ID: mdl-24583013

ABSTRACT

BACKGROUND: Visual information conveyed through the extrageniculate visual pathway, which runs from the retina via the superior colliculus (SC) and the lateral posterior nucleus (LPN) of the thalamus to the higher visual cortex, plays a critical role in the visual capabilities of many mammalian species. However, its functional role in the higher visual cortex remains unclear. Here, we observed visual cortical area activity in anesthetized mice to evaluate the role of the extrageniculate pathway on their specialized visual properties. RESULTS: The preferred stimulus velocities of neurons in the higher visual areas (lateromedial [LM], anterolateral [AL], anteromedial [AM], and rostrolateral [RL] areas) were measured using flavoprotein fluorescence imaging and two-photon calcium imaging and were higher than those in the primary visual cortex (V1). Further, the velocity-tuning properties of the higher visual areas were different from each other. The response activities in these areas decreased after V1 ablation; however, the visual properties' differences were preserved. After SC destruction, these preferences for high velocities disappeared, and their tuning profiles became similar to that of the V1, whereas the tuning profile of the V1 remained relatively normal. Neural tracer experiments revealed that each of these higher visual areas connected with specific subregions of the LPN. CONCLUSIONS: The preservation of visual property differences among the higher visual areas following V1 lesions and their loss following SC lesions indicate that pathways from the SC through the thalamus to higher cortical areas are sufficient to support these differences.


Subject(s)
Visual Cortex/physiology , Visual Pathways/physiology , Animals , Lateral Thalamic Nuclei/physiology , Male , Mice , Mice, Inbred C57BL , Optical Imaging/methods , Photic Stimulation , Retina/physiology , Thalamus/physiology , Visual Perception/physiology
20.
Hippocampus ; 23(7): 559-69, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23418076

ABSTRACT

The laterodorsal nucleus (LDN) of the thalamus provides a prominent afferent projection to the postsubiculum (dorsal presubiculum). To characterize synaptic transmission in this pathway, we placed stimulating electrodes in the LDN and recorded fEPSPs elicited in the postsubiculum of urethane-anesthetized rats. LDN stimulation elicited a source-sink dipole between the deep and superficial layers of the postsubiculum, respectively, consistent with anatomical evidence for the termination of thalamic afferents in the superficial layers of the structure, and the existence of deep layer neurons with apical dendrites extending into these layers. Postsubicular fEPSPs were typically 0.5-1.0 mV in amplitude, with a peak latency of approximately 6 ms. Consistent with anatomical observations, the short onset latency of fEPSPs elicited by LDN stimulation, and their ability to follow a 60-Hz train of stimulation, indicate that the projection is monosynaptic. Paired-pulse stimulation revealed pronounced paired-pulse depression that was maximal at 100 ms, suggesting that initial release probabilities are high at LDN-postsubiculum synapses, in common with many neocortical pathways. A conventional tetanus protocol that yields LTP in hippocampal pathways had no effect on postsubicular fEPSPs, but long-term depression could be induced by 60-Hz stimulation. Drug infusion studies revealed that synaptic transmission in the LDN-postsubiculum projection is predominantly AMPA-receptor mediated. Rats were implanted with indwelling infusion cannulae targeting the postsubiculum, and, after a recovery period, were anaesthetized withurethane, and implanted with stimulating and recording electrodes. Infusion of CNQX almost completely abolished postsubicular fEPSPs, whereas D-AP5 had little effect. However, 60-Hz LTD was blocked by D-AP5 infusion, revealing that this form of synaptic plasticity is NMDA-receptor dependent.


Subject(s)
Excitatory Postsynaptic Potentials/physiology , Lateral Thalamic Nuclei/physiology , Neural Pathways/physiology , Synaptic Transmission/physiology , Animals , Electric Stimulation , Male , Rats
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