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1.
Sci Rep ; 14(1): 2608, 2024 01 31.
Article in English | MEDLINE | ID: mdl-38297144

ABSTRACT

An important question in neuroscience is how sensory systems change as animals grow and interact with the environment. Exploring sensory systems in animals as they develop can reveal how networks of neurons process information as the neurons themselves grow and the needs of the animal change. Here we compared the structure and function of peripheral parts of the olfactory pathway in newly hatched and adult locusts. We found that populations of olfactory sensory neurons (OSNs) in hatchlings and adults responded with similar tunings to a panel of odors. The morphologies of local neurons (LNs) and projection neurons (PNs) in the antennal lobes (ALs) were very similar in both age groups, though they were smaller in hatchlings, they were proportional to overall brain size. The odor evoked responses of LNs and PNs were also very similar in both age groups, characterized by complex patterns of activity including oscillatory synchronization. Notably, in hatchlings, spontaneous and odor-evoked firing rates of PNs were lower, and LFP oscillations were lower in frequency, than in the adult. Hatchlings have smaller antennae with fewer OSNs; removing antennal segments from adults also reduced LFP oscillation frequency. Thus, consistent with earlier computational models, the developmental increase in frequency is due to increasing intensity of input to the oscillation circuitry. Overall, our results show that locusts hatch with a fully formed olfactory system that structurally and functionally matches that of the adult, despite its small size and lack of prior experience with olfactory stimuli.


Subject(s)
Grasshoppers , Olfactory Receptor Neurons , Animals , Odorants , Olfactory Pathways/physiology , Olfactory Receptor Neurons/physiology , Interneurons , Smell/physiology
2.
PLoS One ; 18(7): e0284641, 2023.
Article in English | MEDLINE | ID: mdl-37428771

ABSTRACT

Many animals display innate preferences for some odors, but the physiological mechanisms underlying these preferences are poorly understood. Here, with behavioral tests, we establish a model system well suited to investigating olfactory mechanisms, the locust Schistocerca americana. We conducted open field tests in an arena designed to provide only olfactory cues to guide navigation choices. We found that newly hatched locusts navigated toward, and spent more time near, the odor of wheat grass than humidified air. In similar tests, we found that hatchlings avoided moderate concentrations of major individual components of the food blend odor, 1-hexanol (1% v/v) and hexanal (0.9% v/v) diluted in mineral oil relative to control presentations of unscented mineral oil. Hatchlings were neither attracted nor repelled by a lower concentration (0.1% v/v) of 1-hexanol but were moderately attracted to a low concentration (0.225% v/v) of hexanal. We quantified the behavior of the animals by tracking their positions with the Argos software toolkit. Our results establish that hatchlings have a strong, innate preference for food odor blend, but the valence of the blend's individual components may be different and may change depending on the concentration. Our results provide a useful entry point for an analysis of physiological mechanisms underlying innate sensory preferences.


Subject(s)
Mineral Oil , Odorants , Animals , Smell/physiology
3.
Elife ; 122023 01 31.
Article in English | MEDLINE | ID: mdl-36719272

ABSTRACT

Odorants binding to olfactory receptor neurons (ORNs) trigger bursts of action potentials, providing the brain with its only experience of the olfactory environment. Our recordings made in vivo from locust ORNs showed that odor-elicited firing patterns comprise four distinct response motifs, each defined by a reliable temporal profile. Different odorants could elicit different response motifs from a given ORN, a property we term motif switching. Further, each motif undergoes its own form of sensory adaptation when activated by repeated plume-like odor pulses. A computational model constrained by our recordings revealed that organizing responses into multiple motifs provides substantial benefits for classifying odors and processing complex odor plumes: each motif contributes uniquely to encode the plume's composition and structure. Multiple motifs and motif switching further improve odor classification by expanding coding dimensionality. Our model demonstrated that these response features could provide benefits for olfactory navigation, including determining the distance to an odor source.


Subject(s)
Olfactory Receptor Neurons , Olfactory Receptor Neurons/physiology , Smell/physiology , Odorants , Action Potentials/physiology , Brain
4.
Sci Rep ; 12(1): 22628, 2022 12 31.
Article in English | MEDLINE | ID: mdl-36587060

ABSTRACT

Locusts depend upon their sense of smell and provide useful models for understanding olfaction. Extending this understanding requires knowledge of the molecular and structural organization of the olfactory system. Odor sensing begins with olfactory receptor neurons (ORNs), which express odorant receptors (ORs). In insects, ORNs are housed, in varying numbers, in olfactory sensilla. Because the organization of ORs within sensilla affects their function, it is essential to identify the ORs they contain. Here, using RNA sequencing, we identified 179 putative ORs in the transcriptomes of the two main olfactory organs, antenna and palp, of the locust Schistocerca americana. Quantitative expression analysis showed most putative ORs (140) are expressed in antennae while only 31 are in the palps. Further, our analysis identified one OR detected only in the palps and seven ORs that are expressed differentially by sex. An in situ analysis of OR expression suggested ORs are organized in non-random combinations within antennal sensilla. A phylogenetic comparison of OR predicted protein sequences revealed homologous relationships among two other Acrididae species. Our results provide a foundation for understanding the organization of the first stage of the olfactory system in S. americana, a well-studied model for olfactory processing.


Subject(s)
Grasshoppers , Olfactory Receptor Neurons , Receptors, Odorant , Animals , Receptors, Odorant/metabolism , Phylogeny , Olfactory Receptor Neurons/metabolism , Grasshoppers/genetics , Grasshoppers/metabolism , Sensilla/metabolism , Smell/genetics , Arthropod Antennae/metabolism , Insect Proteins/genetics , Insect Proteins/metabolism
5.
Curr Biol ; 32(9): R420-R423, 2022 05 09.
Article in English | MEDLINE | ID: mdl-35537393

ABSTRACT

Gap junctions, too small to spot in images used to create connectome maps, play outsized roles in shaping neural activity. A recent study reveals a surprising new gap junction function: they can stabilize a neuron's membrane potential against unwanted oscillations.


Subject(s)
Connectome , Neurons , Animals , Connexins , Gap Junctions , Insecta , Membrane Potentials
6.
Methods Ecol Evol ; 13(3): 585-595, 2022 Mar.
Article in English | MEDLINE | ID: mdl-37920569

ABSTRACT

Automatically tracking the positions of multiple animals is often necessary for studying behaviours. This task involves multiple object tracking, a challenging problem in computer vision. Recent advances in machine learning applied to video analysis have been helpful for animal tracking. However, existing tools work well only in homogeneous environments with uniform illumination, features rarely found in natural settings. Moreover, available algorithms cannot effectively process discontinuities in animal motion such as sudden jumps, thus requiring laborious manual review.Here we present Argos, a software toolkit for tracking multiple animals in inhomogeneous environments. Argos includes tools for compressing videos based on animal movement, for generating training sets for a convolutional neural network (CNN) to detect animals, for tracking multiple animals in a video and for facilitating review and correction of the tracks manually, with simple graphical user interfaces.We demonstrate that Argos can help reduce the amount of video data to be stored and analysed, speed up analysis and allow analysing difficult and ambiguous conditions in a scene.Thus, Argos supports multiple approaches to animal tracking suited for varying recording conditions and available computational resources. Together, these tools allow the recording and tracking of movements of multiple markerless animals in inhomogeneous environments over many hours.

7.
Proc Natl Acad Sci U S A ; 117(45): 28102-28113, 2020 11 10.
Article in English | MEDLINE | ID: mdl-33106410

ABSTRACT

Better understanding myelination of peripheral nerves would benefit patients affected by peripheral neuropathies, including Charcot-Marie-Tooth disease. Little is known about the role the Golgi compartment plays in Schwann cell (SC) functions. Here, we studied the role of Golgi in myelination of peripheral nerves in mice through SC-specific genetic inactivation of phosphatidylinositol 4-kinase beta (PI4KB), a Golgi-associated lipid kinase. Sciatic nerves of such mice showed thinner myelin of large diameter axons and gross aberrations in myelin organization affecting the nodes of Ranvier, the Schmidt-Lanterman incisures, and Cajal bands. Nonmyelinating SCs showed a striking inability to engulf small diameter nerve fibers. SCs of mutant mice showed a distorted Golgi morphology and disappearance of OSBP at the cis-Golgi compartment, together with a complete loss of GOLPH3 from the entire Golgi. Accordingly, the cholesterol and sphingomyelin contents of sciatic nerves were greatly reduced and so was the number of caveolae observed in SCs. Although the conduction velocity of sciatic nerves of mutant mice showed an 80% decrease, the mice displayed only subtle impairment in their motor functions. Our analysis revealed that Golgi functions supported by PI4KB are critically important for proper myelination through control of lipid metabolism, protein glycosylation, and organization of microvilli in the nodes of Ranvier of peripheral nerves.


Subject(s)
Golgi Apparatus/metabolism , Minor Histocompatibility Antigens , Myelin Sheath/metabolism , Peripheral Nerves/metabolism , Phosphotransferases (Alcohol Group Acceptor) , Schwann Cells/metabolism , Animals , Cholesterol/metabolism , Mice , Mice, Knockout , Minor Histocompatibility Antigens/genetics , Minor Histocompatibility Antigens/metabolism , Phosphatidylinositols/metabolism , Phosphotransferases (Alcohol Group Acceptor)/genetics , Phosphotransferases (Alcohol Group Acceptor)/metabolism
8.
Elife ; 92020 03 12.
Article in English | MEDLINE | ID: mdl-32163034

ABSTRACT

Inhibitory neurons play critical roles in regulating and shaping olfactory responses in vertebrates and invertebrates. In insects, these roles are performed by relatively few neurons, which can be interrogated efficiently, revealing fundamental principles of olfactory coding. Here, with electrophysiological recordings from the locust and a large-scale biophysical model, we analyzed the properties and functions of GGN, a unique giant GABAergic neuron that plays a central role in structuring olfactory codes in the locust mushroom body. Our simulations suggest that depolarizing GGN at its input branch can globally inhibit KCs several hundred microns away. Our in vivorecordings show that GGN responds to odors with complex temporal patterns of depolarization and hyperpolarization that can vary with odors and across animals, leading our model to predict the existence of a yet-undiscovered olfactory pathway. Our analysis reveals basic new features of GGN and the olfactory network surrounding it.


Subject(s)
Feedback, Physiological/physiology , Grasshoppers/physiology , Smell/physiology , Animals , Computer Simulation , Female , Grasshoppers/anatomy & histology , Male , Models, Biological , Neurons/physiology
9.
PLoS Comput Biol ; 16(2): e1007461, 2020 02.
Article in English | MEDLINE | ID: mdl-32012160

ABSTRACT

The neural representation of a stimulus is repeatedly transformed as it moves from the sensory periphery to deeper layers of the nervous system. Sparsening transformations are thought to increase the separation between similar representations, encode stimuli with great specificity, maximize storage capacity of associative memories, and provide an energy efficient instantiation of information in neural circuits. In the insect olfactory system, odors are initially represented in the periphery as a combinatorial code with relatively simple temporal dynamics. Subsequently, in the antennal lobe this representation is transformed into a dense and complex spatiotemporal activity pattern. Next, in the mushroom body Kenyon cells (KCs), the representation is dramatically sparsened. Finally, in mushroom body output neurons (MBONs), the representation takes on a new dense spatiotemporal format. Here, we develop a computational model to simulate this chain of olfactory processing from the receptor neurons to MBONs. We demonstrate that representations of similar odorants are maximally separated, measured by the distance between the corresponding MBON activity vectors, when KC responses are sparse. Sparseness is maintained across variations in odor concentration by adjusting the feedback inhibition that KCs receive from an inhibitory neuron, the Giant GABAergic neuron. Different odor concentrations require different strength and timing of feedback inhibition for optimal processing. Importantly, as observed in vivo, the KC-MBON synapse is highly plastic, and, therefore, changes in synaptic strength after learning can change the balance of excitation and inhibition, potentially leading to changes in the distance between MBON activity vectors of two odorants for the same level of KC population sparseness. Thus, what is an optimal degree of sparseness before odor learning, could be rendered sub-optimal post learning. Here, we show, however, that synaptic weight changes caused by spike timing dependent plasticity increase the distance between the odor representations from the perspective of MBONs. A level of sparseness that was optimal before learning remains optimal post-learning.


Subject(s)
Neuronal Plasticity , Olfactory Pathways/physiology , Smell , Animals , Humans
10.
Curr Biol ; 28(13): R757-R759, 2018 07 09.
Article in English | MEDLINE | ID: mdl-29990462

ABSTRACT

New studies show that, as in mammals, perceptual decision-making behavior in fruit flies involves the integration of sensory information that accumulates over time; this involves a process of dendritic integration that depends on the transcription factor FoxP.


Subject(s)
Drosophila , Smell , Animals , Decision Making , Dendrites
11.
Front Neural Circuits ; 12: 49, 2018.
Article in English | MEDLINE | ID: mdl-29950976

ABSTRACT

[This corrects the article on p. 30 in vol. 11, PMID: 28515683.].

12.
Cell Rep ; 23(10): 2881-2890, 2018 06 05.
Article in English | MEDLINE | ID: mdl-29874576

ABSTRACT

Active membrane remodeling during myelination relies on phospholipid synthesis and membrane polarization, both of which are known to depend on inositol phospholipids. Here, we show that sciatic nerves of mice lacking phosphatidylinositol 4-kinase alpha (PI4KA) in Schwann cells (SCs) show substantially reduced myelin thickness with grave consequences on nerve conductivity and motor functions. Surprisingly, prolonged inhibition of PI4KA in immortalized mouse SCs failed to decrease plasma membrane phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2) levels or PI 3-kinase (PI3K) activation, in spite of large reductions in plasma membrane PI4P levels. Instead, it caused rearrangements of the actin cytoskeleton, which was also observed in sciatic nerves of knockout animals. PI4KA inactivation disproportionally reduced phosphatidylserine, phosphatidylethanolamine, and sphingomyelin content in mutant nerves, with similar changes observed in SCs treated with a PI4KA inhibitor. These studies define a role for PI4KA in myelin formation primarily affecting metabolism of key phospholipids and the actin cytoskeleton.


Subject(s)
Gene Deletion , Minor Histocompatibility Antigens/metabolism , Myelin Sheath/pathology , Phosphotransferases (Alcohol Group Acceptor)/metabolism , Schwann Cells/enzymology , Actins/metabolism , Animals , Cell Line , Cell Membrane/metabolism , Cell Movement , Enzyme Activation , Mice, Knockout , Mutation/genetics , Myelin Sheath/metabolism , Phosphatidylinositol 3-Kinases/metabolism , Phosphatidylinositol 4,5-Diphosphate/metabolism , Phosphatidylinositol Phosphates/metabolism , Proto-Oncogene Proteins c-akt/metabolism , Sciatic Nerve/metabolism , Sciatic Nerve/pathology , Sciatic Nerve/ultrastructure , Sphingolipids/metabolism , TOR Serine-Threonine Kinases/metabolism
13.
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
14.
Front Neural Circuits ; 11: 30, 2017.
Article in English | MEDLINE | ID: mdl-28515683

ABSTRACT

In the insect olfactory system, odor information is transferred from the antennal lobe (AL) to higher brain areas by projection neurons (PNs) in multiple AL tracts (ALTs). In several species, one of the ALTs, the mediolateral ALT (mlALT), contains some GABAergic PNs; in the Drosophila brain, the great majority of ventral PNs (vPNs) are GABAergic and project through this tract to the lateral horn (LH). Most excitatory PNs (ePNs), project through the medial ALT (mALT) to the mushroom body (MB) and the LH. Recent studies have shown that GABAergic vPNs play inhibitory roles at their axon terminals in the LH. However, little is known about the properties and functions of vPNs at their dendritic branches in the AL. Here, we used optogenetic and patch clamp techniques to investigate the functional roles of vPNs in the AL. Surprisingly, our results show that specific activation of vPNs reliably elicits strong excitatory postsynaptic potentials (EPSPs) in ePNs. Moreover, the connections between vPNs and ePNs are mediated by direct chemical synapses. Neither pulses of GABA, nor pharmagological, or genetic blockade of GABAergic transmission gave results consistent with the involvement of GABA in vPN-ePN excitatory transmission. These unexpected results suggest new roles for the vPN population in olfactory information processing.


Subject(s)
Excitatory Postsynaptic Potentials/physiology , Mushroom Bodies/cytology , Neural Inhibition/physiology , Olfactory Bulb/cytology , Olfactory Receptor Neurons/physiology , Synapses/physiology , Action Potentials/drug effects , Action Potentials/physiology , Animals , Animals, Genetically Modified , Cadmium Chloride/pharmacology , Drosophila , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Excitatory Postsynaptic Potentials/drug effects , GABA Antagonists/pharmacology , Luminescent Proteins/genetics , Luminescent Proteins/metabolism , Neural Inhibition/drug effects , Neural Inhibition/genetics , Odorants , Olfactory Receptor Neurons/drug effects , Picrotoxin/pharmacology , RNA Interference/physiology , Sodium Channel Blockers/pharmacology , Synapses/drug effects , Synapses/genetics , Tetrodotoxin/pharmacology , gamma-Aminobutyric Acid/pharmacology
15.
Nat Commun ; 7: 13808, 2016 12 15.
Article in English | MEDLINE | ID: mdl-27976720

ABSTRACT

Oscillatory synchrony among neurons occurs in many species and brain areas, and has been proposed to help neural circuits process information. One hypothesis states that oscillatory input creates cyclic integration windows: specific times in each oscillatory cycle when postsynaptic neurons become especially responsive to inputs. With paired local field potential (LFP) and intracellular recordings and controlled stimulus manipulations we directly test this idea in the locust olfactory system. We find that inputs arriving in Kenyon cells (KCs) sum most effectively in a preferred window of the oscillation cycle. With a computational model, we show that the non-uniform structure of noise in the membrane potential helps mediate this process. Further experiments performed in vivo demonstrate that integration windows can form in the absence of inhibition and at a broad range of oscillation frequencies. Our results reveal how a fundamental coincidence-detection mechanism in a neural circuit functions to decode temporally organized spiking.


Subject(s)
Membrane Potentials/physiology , Mushroom Bodies/cytology , Neurons/physiology , Smell/physiology , Animals , Grasshoppers , Models, Neurological , Models, Theoretical , Noise , Patch-Clamp Techniques
16.
J Neurophysiol ; 115(5): 2303-16, 2016 05 01.
Article in English | MEDLINE | ID: mdl-26864765

ABSTRACT

Olfactory processing takes place across multiple layers of neurons from the transduction of odorants in the periphery, to odor quality processing, learning, and decision making in higher olfactory structures. In insects, projection neurons (PNs) in the antennal lobe send odor information to the Kenyon cells (KCs) of the mushroom bodies and lateral horn neurons (LHNs). To examine the odor information content in different structures of the insect brain, antennal lobe, mushroom bodies and lateral horn, we designed a model of the olfactory network based on electrophysiological recordings made in vivo in the locust. We found that populations of all types (PNs, LHNs, and KCs) had lower odor classification error rates than individual cells of any given type. This improvement was quantitatively different from that observed using uniform populations of identical neurons compared with spatially structured population of neurons tuned to different odor features. This result, therefore, reflects an emergent network property. Odor classification improved with increasing stimulus duration: for similar odorants, KC and LHN ensembles reached optimal discrimination within the first 300-500 ms of the odor response. Performance improvement with time was much greater for a population of cells than for individual neurons. We conclude that, for PNs, LHNs, and KCs, ensemble responses are always much more informative than single-cell responses, despite the accumulation of noise along with odor information.


Subject(s)
Discrimination, Psychological , Olfactory Pathways/physiology , Olfactory Perception , Sensory Receptor Cells/physiology , Animals , Grasshoppers , Mushroom Bodies/cytology , Mushroom Bodies/physiology , Odorants , Olfactory Pathways/cytology
17.
Mol Neurobiol ; 53(5): 3477-3493, 2016 07.
Article in English | MEDLINE | ID: mdl-26093382

ABSTRACT

In early postnatal development, naturally occurring cell death, dendritic outgrowth, and synaptogenesis sculpt neuronal ensembles into functional neuronal circuits. Here, we demonstrate that deletion of the extracellular proteinase matrix metalloproteinase-9 (MMP-9) affects each of these processes, resulting in maladapted neuronal circuitry. MMP-9 deletion increases the number of CA1 pyramidal neurons but decreases dendritic length and complexity. Parallel changes in neuronal morphology are observed in primary visual cortex and persist into adulthood. Individual CA1 neurons in MMP-9(-/-) mice have enhanced input resistance and a significant increase in the frequency, but not amplitude, of miniature excitatory postsynaptic currents (mEPSCs). Additionally, deletion of MMP-9 significantly increases spontaneous neuronal activity in awake MMP-9(-/-) mice and enhances response to acute challenge by the excitotoxin kainate. Our data document a novel role for MMP-9-dependent proteolysis: the regulation of several aspects of circuit maturation to constrain excitability throughout life.


Subject(s)
Matrix Metalloproteinase 9/metabolism , Nerve Net/enzymology , Nerve Net/physiology , Neurons/enzymology , Neurons/physiology , Animals , Animals, Newborn , Biomarkers/metabolism , Cell Death , Dendritic Spines/metabolism , Dendritic Spines/pathology , Female , Hippocampus/pathology , Hippocampus/physiopathology , Kainic Acid , Male , Matrix Metalloproteinase 9/deficiency , Mice, Inbred C57BL , Neurons/pathology , Proto-Oncogene Proteins c-fos/metabolism , Pyramidal Cells/metabolism , Pyramidal Cells/pathology , Seizures/pathology , Seizures/physiopathology , Synapses/metabolism , Synaptic Transmission
18.
PLoS Comput Biol ; 11(10): e1004531, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26458212

ABSTRACT

Inhibitory interneurons play critical roles in shaping the firing patterns of principal neurons in many brain systems. Despite difference in the anatomy or functions of neuronal circuits containing inhibition, two basic motifs repeatedly emerge: feed-forward and feedback. In the locust, it was proposed that a subset of lateral horn interneurons (LHNs), provide feed-forward inhibition onto Kenyon cells (KCs) to maintain their sparse firing--a property critical for olfactory learning and memory. But recently it was established that a single inhibitory cell, the giant GABAergic neuron (GGN), is the main and perhaps sole source of inhibition in the mushroom body, and that inhibition from this cell is mediated by a feedback (FB) loop including KCs and the GGN. To clarify basic differences in the effects of feedback vs. feed-forward inhibition in circuit dynamics we here use a model of the locust olfactory system. We found both inhibitory motifs were able to maintain sparse KCs responses and provide optimal odor discrimination. However, we further found that only FB inhibition could create a phase response consistent with data recorded in vivo. These findings describe general rules for feed-forward versus feedback inhibition and suggest GGN is potentially capable of providing the primary source of inhibition to the KCs. A better understanding of how inhibitory motifs impact post-synaptic neuronal activity could be used to reveal unknown inhibitory structures within biological networks.


Subject(s)
Feedback, Physiological/physiology , Models, Neurological , Nerve Net/physiology , Neural Inhibition/physiology , Olfactory Pathways/physiology , Smell/physiology , Action Potentials/physiology , Animals , Computer Simulation , Excitatory Postsynaptic Potentials/physiology , Grasshoppers/physiology , Mushroom Bodies/physiology , Synaptic Transmission/physiology
19.
Neuron ; 88(2): 403-18, 2015 Oct 21.
Article in English | MEDLINE | ID: mdl-26456047

ABSTRACT

Sensory inputs are often fluctuating and intermittent, yet animals reliably utilize them to direct behavior. Here we ask how natural stimulus fluctuations influence the dynamic neural encoding of odors. Using the locust olfactory system, we isolated two main causes of odor intermittency: chaotic odor plumes and active sampling behaviors. Despite their irregularity, chaotic odor plumes still drove dynamic neural response features including the synchronization, temporal patterning, and short-term plasticity of spiking in projection neurons, enabling classifier-based stimulus identification and activating downstream decoders (Kenyon cells). Locusts can also impose odor intermittency through active sampling movements with their unrestrained antennae. Odors triggered immediate, spatially targeted antennal scanning that, paradoxically, weakened individual neural responses. However, these frequent but weaker responses were highly informative about stimulus location. Thus, not only are odor-elicited dynamic neural responses compatible with natural stimulus fluctuations and important for stimulus identification, but locusts actively increase intermittency, possibly to improve stimulus localization.


Subject(s)
Arthropod Antennae/physiology , Odorants , Olfactory Pathways/physiology , Olfactory Receptor Neurons/physiology , Smell/physiology , Animals , Female , Grasshoppers , Male
20.
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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