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1.
PNAS Nexus ; 3(1): pgad481, 2024 Jan.
Article in English | MEDLINE | ID: mdl-38213615

ABSTRACT

Although diurnal animals displaying monophasic sleep patterns exhibit periodic cycles of alternating slow-wave sleep (SWS) and rapid eye movement sleep (REMS), the regulatory mechanisms underlying these regular sleep cycles remain unclear. Here, we report that in the Australian dragon Pogona vitticeps exposed to constant darkness (DD), sleep behavior and sleep-related neuronal activity emerged over a 24-h cycle. However, the regularity of the REMS/SWS alternation was disrupted under these conditions. Notably, when the lizards were then exposed to 12 h of light after DD, the regularity of the sleep stages was restored. These results suggest that sleep-related neuronal activity in lizards is regulated by circadian rhythms and that the regularity of REMS and SWS cycling is influenced by daytime light exposure.

2.
Nature ; 619(7968): 129-134, 2023 Jul.
Article in English | MEDLINE | ID: mdl-37380770

ABSTRACT

While sleeping, many vertebrate groups alternate between at least two sleep stages: rapid eye movement and slow wave sleep1-4, in part characterized by wake-like and synchronous brain activity, respectively. Here we delineate neural and behavioural correlates of two stages of sleep in octopuses, marine invertebrates that evolutionarily diverged from vertebrates roughly 550 million years ago (ref. 5) and have independently evolved large brains and behavioural sophistication. 'Quiet' sleep in octopuses is rhythmically interrupted by approximately 60-s bouts of pronounced body movements and rapid changes in skin patterning and texture6. We show that these bouts are homeostatically regulated, rapidly reversible and come with increased arousal threshold, representing a distinct 'active' sleep stage. Computational analysis of active sleep skin patterning reveals diverse dynamics through a set of patterns conserved across octopuses and strongly resembling those seen while awake. High-density electrophysiological recordings from the central brain reveal that the local field potential (LFP) activity during active sleep resembles that of waking. LFP activity differs across brain regions, with the strongest activity during active sleep seen in the superior frontal and vertical lobes, anatomically connected regions associated with learning and memory function7-10. During quiet sleep, these regions are relatively silent but generate LFP oscillations resembling mammalian sleep spindles11,12 in frequency and duration. The range of similarities with vertebrates indicates that aspects of two-stage sleep in octopuses may represent convergent features of complex cognition.


Subject(s)
Central Nervous System , Integumentary System , Octopodiformes , Sleep , Wakefulness , Animals , Mammals/physiology , Octopodiformes/physiology , Sleep/physiology , Sleep, REM/physiology , Wakefulness/physiology , Integumentary System/innervation , Integumentary System/physiology , Movement/physiology , Time Factors , Local Field Potential Measurement , Learning/physiology , Central Nervous System/anatomy & histology , Central Nervous System/physiology , Arousal/physiology
3.
Nature ; 619(7968): 122-128, 2023 Jul.
Article in English | MEDLINE | ID: mdl-37380772

ABSTRACT

Many cephalopods escape detection using camouflage1. This behaviour relies on a visual assessment of the surroundings, on an interpretation of visual-texture statistics2-4 and on matching these statistics using millions of skin chromatophores that are controlled by motoneurons located in the brain5-7. Analysis of cuttlefish images proposed that camouflage patterns are low dimensional and categorizable into three pattern classes, built from a small repertoire of components8-11. Behavioural experiments also indicated that, although camouflage requires vision, its execution does not require feedback5,12,13, suggesting that motion within skin-pattern space is stereotyped and lacks the possibility of correction. Here, using quantitative methods14, we studied camouflage in the cuttlefish Sepia officinalis as behavioural motion towards background matching in skin-pattern space. An analysis of hundreds of thousands of images over natural and artificial backgrounds revealed that the space of skin patterns is high-dimensional and that pattern matching is not stereotyped-each search meanders through skin-pattern space, decelerating and accelerating repeatedly before stabilizing. Chromatophores could be grouped into pattern components on the basis of their covariation during camouflaging. These components varied in shapes and sizes, and overlay one another. However, their identities varied even across transitions between identical skin-pattern pairs, indicating flexibility of implementation and absence of stereotypy. Components could also be differentiated by their sensitivity to spatial frequency. Finally, we compared camouflage to blanching, a skin-lightening reaction to threatening stimuli. Pattern motion during blanching was direct and fast, consistent with open-loop motion in low-dimensional pattern space, in contrast to that observed during camouflage.


Subject(s)
Behavior, Animal , Environment , Sepia , Skin Pigmentation , Animals , Behavior, Animal/physiology , Sepia/physiology , Skin Pigmentation/physiology
5.
Nature ; 578(7795): 413-418, 2020 02.
Article in English | MEDLINE | ID: mdl-32051589

ABSTRACT

The mammalian claustrum, owing to its widespread connectivity with other forebrain structures, has been hypothesized to mediate functions that range from decision-making to consciousness1. Here we report that a homologue of the claustrum, identified by single-cell transcriptomics and viral tracing of connectivity, also exists in a reptile-the Australian bearded dragon Pogona vitticeps. In Pogona, the claustrum underlies the generation of sharp waves during slow-wave sleep. The sharp waves, together with superimposed high-frequency ripples2, propagate to the entire neighbouring pallial dorsal ventricular ridge (DVR). Unilateral or bilateral lesions of the claustrum suppress the production of sharp-wave ripples during slow-wave sleep in a unilateral or bilateral manner, respectively, but do not affect the regular and rapidly alternating sleep rhythm that is characteristic of sleep in this species3. The claustrum is thus not involved in the generation of the sleep rhythm itself. Tract tracing revealed that the reptilian claustrum projects widely to a variety of forebrain areas, including the cortex, and that it receives converging inputs from, among others, areas of the mid- and hindbrain that are known to be involved in wake-sleep control in mammals4-6. Periodically modulating the concentration of serotonin in the claustrum, for example, caused a matching modulation of sharp-wave production there and in the neighbouring DVR. Using transcriptomic approaches, we also identified a claustrum in the turtle Trachemys scripta, a distant reptilian relative of lizards. The claustrum is therefore an ancient structure that was probably already present in the brain of the common vertebrate ancestor of reptiles and mammals. It may have an important role in the control of brain states owing to the ascending input it receives from the mid- and hindbrain, its widespread projections to the forebrain and its role in sharp-wave generation during slow-wave sleep.


Subject(s)
Claustrum/anatomy & histology , Claustrum/physiology , Lizards/anatomy & histology , Lizards/physiology , Sleep/physiology , Animals , Claustrum/cytology , Claustrum/injuries , Male , Mammals/physiology , Mesencephalon/cytology , Mesencephalon/physiology , Neural Pathways , RNA-Seq , Rhombencephalon/cytology , Rhombencephalon/physiology , Serotonin/metabolism , Single-Cell Analysis , Transcriptome , Turtles/anatomy & histology , Turtles/physiology
6.
Curr Opin Neurobiol ; 60: 47-54, 2020 02.
Article in English | MEDLINE | ID: mdl-31837480

ABSTRACT

Visual perception is inherently statistical: brains exploit repeating features of natural scenes to disambiguate images that could, in principle, have many causes. A clear case for the relevance of statistical inference in vision is animal camouflage. Although visual scenes are each composed of unique arrangements of pixels, they are usually perceived mainly as groupings of statistically defined patches (sandy/leafy/smooth etc…); this fact is exploited by camouflaging animals. The unique ability of certain cephalopods to camouflage actively within many different surroundings provides a rare and direct behavioral readout for texture perception. In addition, because cephalopods and chordates each arose after a phylogenetic split that occurred some 600M years ago, the apparent convergence of texture perception across these groups suggests common principles. Studying cephalopod camouflage may thus help us resolve general problems of visual perception.


Subject(s)
Decapodiformes , Visual Perception , Animals , Phylogeny , Vision, Ocular
7.
Nature ; 562(7727): 361-366, 2018 10.
Article in English | MEDLINE | ID: mdl-30333578

ABSTRACT

Few animals provide a readout that is as objective of their perceptual state as camouflaging cephalopods. Their skin display system includes an extensive array of pigment cells (chromatophores), each expandable by radial muscles controlled by motor neurons. If one could track the individual expansion states of the chromatophores, one would obtain a quantitative description-and potentially even a neural description by proxy-of the perceptual state of the animal in real time. Here we present the use of computational and analytical methods to achieve this in behaving animals, quantifying the states of tens of thousands of chromatophores at sixty frames per second, at single-cell resolution, and over weeks. We infer a statistical hierarchy of motor control, reveal an underlying low-dimensional structure to pattern dynamics and uncover rules that govern the development of skin patterns. This approach provides an objective description of complex perceptual behaviour, and a powerful means to uncover the organizational principles that underlie the function, dynamics and morphogenesis of neural systems.


Subject(s)
Biological Mimicry/physiology , Chromatophores/physiology , Decapodiformes/physiology , Skin Physiological Phenomena , Animals , Behavior, Animal , Color , Decapodiformes/cytology , Models, Biological , Motor Neurons/physiology , Single-Cell Analysis , Skin/cytology
8.
Brain Behav Evol ; 90(1): 41-52, 2017.
Article in English | MEDLINE | ID: mdl-28866680

ABSTRACT

Our ability to navigate through the world depends on the function of the hippocampus. This old cortical structure plays a critical role in spatial navigation in mammals and in a variety of processes, including declarative and episodic memory and social behavior. Intense research has revealed much about hippocampal anatomy, physiology, and computation; yet, even intensely studied phenomena such as the shaping of place cell activity or the function of hippocampal firing patterns during sleep remain incompletely understood. Interestingly, while the hippocampus may be a 'higher order' area linked to a complex cortical hierarchy in mammals, it is an old cortical structure in evolutionary terms. The reptilian cortex, structurally much simpler than the mammalian cortex and hippocampus, therefore presents a good alternative model for exploring hippocampal function. Here, we trace common patterns in the evolution of the hippocampus of reptiles and mammals and ask which parts can be profitably compared to understand functional principles. In addition, we describe a selection of the highly diverse repertoire of reptilian behaviors to illustrate the value of a comparative approach towards understanding hippocampal function.


Subject(s)
Biological Evolution , Hippocampus/anatomy & histology , Reptiles/anatomy & histology , Animals , Hippocampus/physiology , Humans , Reptiles/physiology , Spatial Memory/physiology , Spatial Navigation/physiology
9.
J Vis Exp ; (124)2017 06 29.
Article in English | MEDLINE | ID: mdl-28715373

ABSTRACT

The sense of taste allows animals to detect chemicals in the environment, giving rise to behaviors critical for survival. When Gustatory Receptor Neurons (GRNs) detect tastant molecules, they encode information about the identity and concentration of the tastant as patterns of electrical activity that then propagate to follower neurons in the brain. These patterns constitute internal representations of the tastant, which then allow the animal to select actions and form memories. The use of relatively simple animal models has been a powerful tool to study basic principles in sensory coding. Here, we propose three new methods to study gustatory coding using the moth Manduca sexta. First, we present a dissection procedure for exposing the maxillary nerves and the subesophageal zone (SEZ), allowing recording of the activity of GRNs from their axons. Second, we describe the use of extracellular electrodes to record the activity of multiple GRNs by placing tetrode wires directly into the maxillary nerve. Third, we present a new system for delivering and monitoring, with high temporal precision, pulses of different tastants. These methods allow the characterization of neuronal responses in vivo directly from GRNs before, during and after tastants are delivered. We provide examples of voltage traces recorded from multiple GRNs, and present an example of how a spike sorting technique can be applied to the data to identify the responses of individual neurons. Finally, to validate our recording approach, we compare extracellular recordings obtained from GRNs with tetrodes to intracellular recordings obtained with sharp glass electrodes.


Subject(s)
Taste/physiology , Animals , Manduca
10.
Science ; 352(6285): 590-5, 2016 Apr 29.
Article in English | MEDLINE | ID: mdl-27126045

ABSTRACT

Sleep has been described in animals ranging from worms to humans. Yet the electrophysiological characteristics of brain sleep, such as slow-wave (SW) and rapid eye movement (REM) activities, are thought to be restricted to mammals and birds. Recording from the brain of a lizard, the Australian dragon Pogona vitticeps, we identified SW and REM sleep patterns, thus pushing back the probable evolution of these dynamics at least to the emergence of amniotes. The SW and REM sleep patterns that we observed in lizards oscillated continuously for 6 to 10 hours with a period of ~80 seconds. The networks controlling SW-REM antagonism in amniotes may thus originate from a common, ancient oscillator circuit. Lizard SW dynamics closely resemble those observed in rodent hippocampal CA1, yet they originate from a brain area, the dorsal ventricular ridge, that has no obvious hodological similarity with the mammalian hippocampus.


Subject(s)
Brain/physiology , Lizards/physiology , Sleep, REM/physiology , Animals , Biological Evolution , CA1 Region, Hippocampal/physiology
11.
J Neurosci ; 35(35): 12309-21, 2015 Sep 02.
Article in English | MEDLINE | ID: mdl-26338341

ABSTRACT

Four of the five major sensory systems (vision, olfaction, somatosensation, and audition) are thought to use different but partially overlapping sets of neurons to form unique representations of vast numbers of stimuli. The only exception is gustation, which is thought to represent only small numbers of basic taste categories. However, using new methods for delivering tastant chemicals and making electrophysiological recordings from the tractable gustatory system of the moth Manduca sexta, we found chemical-specific information is as follows: (1) initially encoded in the population of gustatory receptor neurons as broadly distributed spatiotemporal patterns of activity; (2) dramatically integrated and temporally transformed as it propagates to monosynaptically connected second-order neurons; and (3) observed in tastant-specific behavior. Our results are consistent with an emerging view of the gustatory system: rather than constructing basic taste categories, it uses a spatiotemporal population code to generate unique neural representations of individual tastant chemicals. SIGNIFICANCE STATEMENT: Our results provide a new view of taste processing. Using a new, relatively simple model system and a new set of techniques to deliver taste stimuli and to examine gustatory receptor neurons and their immediate followers, we found no evidence for labeled line connectivity, or basic taste categories such as sweet, salty, bitter, and sour. Rather, individual tastant chemicals are represented as patterns of spiking activity distributed across populations of receptor neurons. These representations are transformed substantially as multiple types of receptor neurons converge upon follower neurons, leading to a combinatorial coding format that uniquely, rapidly, and efficiently represents individual taste chemicals. Finally, we found that the information content of these neurons can drive tastant-specific behavior.


Subject(s)
Chemoreceptor Cells/physiology , Sense Organs/cytology , Synapses/physiology , Taste/physiology , Action Potentials/physiology , Afferent Pathways/physiology , Animals , Chemoreceptor Cells/ultrastructure , Dose-Response Relationship, Drug , Electrophysiology , Female , Male , Manduca , Microscopy, Electron, Scanning , Reaction Time/physiology , Sodium Chloride/pharmacology , Stimulation, Chemical , Sucrose/pharmacology , Synapses/ultrastructure , Time Factors
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