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1.
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
2.
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
3.
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
4.
J Neurosci ; 35(4): 1521-9, 2015 Jan 28.
Article in English | MEDLINE | ID: mdl-25632129

ABSTRACT

As information about the sensory environment passes between layers within the nervous system, the format of the information often changes. To examine how information format affects the capacity of neurons to represent stimuli, we measured the rate of information transmission in olfactory neurons in intact, awake locusts (Schistocerca americana) while pharmacologically manipulating patterns of correlated neuronal activity. Blocking the periodic inhibition underlying odor-elicited neural oscillatory synchronization increased information transmission rates. This suggests oscillatory synchrony, which serves other information processing roles, comes at a cost to the speed with which neurons can transmit information. Our results provide an example of a trade-off between benefits and costs in neural information processing.


Subject(s)
Action Potentials/physiology , Models, Neurological , Neurons/physiology , Olfactory Bulb/cytology , Olfactory Bulb/physiology , Action Potentials/drug effects , Animals , Arthropod Antennae/cytology , Arthropod Antennae/physiology , Computer Simulation , Female , GABA-A Receptor Antagonists/pharmacology , Grasshoppers , Male , Neural Inhibition/physiology , Neurons/drug effects , Nonlinear Dynamics , Odorants , Olfactory Bulb/drug effects , Picrotoxin/pharmacology , Principal Component Analysis
5.
J Exp Biol ; 217(Pt 13): 2301-8, 2014 Jul 01.
Article in English | MEDLINE | ID: mdl-24737754

ABSTRACT

Flying insects rapidly stabilize after perturbations using both visual and mechanosensory inputs for active control. Insect halteres are mechanosensory organs that encode inertial forces to aid rapid course correction during flight but serve no aerodynamic role and are specific to two orders of insects (Diptera and Strepsiptera). Aside from the literature on halteres and recent work on the antennae of the hawkmoth Manduca sexta, it is unclear how other flying insects use mechanosensory information to control body dynamics. The mechanosensory structures found on the halteres, campaniform sensilla, are also present on wings, suggesting that the wings can encode information about flight dynamics. We show that the neurons innervating these sensilla on the forewings of M. sexta exhibit spike-timing precision comparable to that seen in previous reports of campaniform sensilla, including haltere neurons. In addition, by attaching magnets to the wings of moths and subjecting these animals to a simulated pitch stimulus via a rotating magnetic field during tethered flight, we elicited the same vertical abdominal flexion reflex these animals exhibit in response to visual or inertial pitch stimuli. Our results indicate that, in addition to their role as actuators during locomotion, insect wings serve as sensors that initiate reflexes that control body dynamics.


Subject(s)
Flight, Animal , Manduca/physiology , Wings, Animal/physiology , Animals , Biomechanical Phenomena , Feedback, Sensory , Female , Male , Manduca/ultrastructure , Microscopy, Electron, Scanning , Posture , Reflex , Sensilla/physiology , Sensilla/ultrastructure , Wings, Animal/ultrastructure
6.
Curr Biol ; 22(7): R227-9, 2012 Apr 10.
Article in English | MEDLINE | ID: mdl-22497937

ABSTRACT

A recent study in the locust olfactory system shows how neuromodulators can alter the rules of synaptic plasticity to form associative memories through the use of 'tagged' synapses.


Subject(s)
Grasshoppers/physiology , Neuronal Plasticity , Action Potentials , Animals , Grasshoppers/drug effects , Memory , Neurotransmitter Agents/pharmacology , Odorants/analysis , Smell , Synapses/drug effects , Synapses/metabolism
7.
PLoS One ; 7(1): e30115, 2012.
Article in English | MEDLINE | ID: mdl-22253900

ABSTRACT

What are the fundamental constraints on the precision and accuracy with which nervous systems can process information? One constraint must reflect the intrinsic "noisiness" of the mechanisms that transmit information between nerve cells. Most neurons transmit information through the probabilistic generation and propagation of spikes along axons, and recent modeling studies suggest that noise from spike propagation might pose a significant constraint on the rate at which information could be transmitted between neurons. However, the magnitude and functional significance of this noise source in actual cells remains poorly understood. We measured variability in conduction time along the axons of identified neurons in the cercal sensory system of the cricket Acheta domesticus, and used information theory to calculate the effects of this variability on sensory coding. We found that the variability in spike propagation speed is not large enough to constrain the accuracy of neural encoding in this system.


Subject(s)
Axons/physiology , Gryllidae/physiology , Information Theory , Interneurons/physiology , Models, Neurological , Neural Conduction/physiology , Action Potentials/physiology , Animals , Female , Nonlinear Dynamics , Physical Stimulation , Stochastic Processes
8.
J Neurosci Methods ; 204(2): 355-65, 2012 Mar 15.
Article in English | MEDLINE | ID: mdl-22155384

ABSTRACT

We developed microfabricated flexible neural probes (FNPs) to provide a bi-directional electrical link to the moth Manduca sexta. These FNPs can deliver electrical stimuli to, and capture neural activity from, the insect's central nervous system. They are comprised of two layers of polyimide with gold sandwiched in between in a split-ring geometry that incorporates the bi-cylindrical anatomical structure of the insect's ventral nerve cord. The FNPs provide consistent left and right abdominal stimulation both across animals and within an individual animal. The features of the stimulation (direction, threshold charge) are aligned with anatomical features of the moth. We also have used these FNPs to record neuronal activity in the ventral nerve cord of the moth. Finally, by integrating carbon nanotube (CNT)-Au nanocomposites into the FNPs we have reduced the interfacial impedance between the probe and the neural tissue, thus reducing the magnitude of stimulation voltage. This in turn allows use of the FNPs with a wireless stimulator, enabling stimulation and flight biasing of freely flying moths. Together, these FNPs present a potent new platform for manipulating and measuring the neural circuitry of insects, and for other nerves in humans and other animals with similar dimensions as the ventral nerve cord of the moth.


Subject(s)
Manduca/physiology , Nanotubes, Carbon , Nervous System/cytology , Neurons/physiology , User-Computer Interface , Action Potentials/physiology , Animals , Biophysics , Electric Stimulation , Electrodes, Implanted , Flight, Animal/physiology , Telemetry/instrumentation , Telemetry/methods
9.
PLoS Comput Biol ; 7(5): e1002041, 2011 May.
Article in English | MEDLINE | ID: mdl-21573206

ABSTRACT

We examined the extent to which temporal encoding may be implemented by single neurons in the cercal sensory system of the house cricket Acheta domesticus. We found that these neurons exhibit a greater-than-expected coding capacity, due in part to an increased precision in brief patterns of action potentials. We developed linear and non-linear models for decoding the activity of these neurons. We found that the stimuli associated with short-interval patterns of spikes (ISIs of 8 ms or less) could be predicted better by second-order models as compared to linear models. Finally, we characterized the difference between these linear and second-order models in a low-dimensional subspace, and showed that modification of the linear models along only a few dimensions improved their predictive power to parity with the second order models. Together these results show that single neurons are capable of using temporal patterns of spikes as fundamental symbols in their neural code, and that they communicate specific stimulus distributions to subsequent neural structures.


Subject(s)
Gryllidae/physiology , Models, Neurological , Neurons/physiology , Action Potentials/physiology , Animals , Computational Biology , Computer Simulation , Female , Information Theory , Linear Models , Nervous System Physiological Phenomena , Nonlinear Dynamics , Time Factors
10.
J Comput Neurosci ; 30(1): 163-79, 2011 Feb.
Article in English | MEDLINE | ID: mdl-20730481

ABSTRACT

We present an application of the information distortion approach to neural coding. The approach allows the discovery of neural symbols and the corresponding stimulus space of a neuron or neural ensemble simultaneously and quantitatively, making few assumptions about the nature of either code or relevant features. The neural codebook is derived by quantitizing sensory stimuli and neural responses into small reproduction sets, and optimizing the quantization to minimize the information distortion function. The application of this approach to the analysis of coding in sensory interneurons involved a further restriction of the space of allowed quantitizers to a smaller family of parametric distributions. We show that, for some cells in this system, a significant amount of information is encoded in patterns of spikes that would not be discovered through analyses based on linear stimulus-response measures.


Subject(s)
Information Theory , Models, Neurological , Sensory Receptor Cells/physiology , Algorithms , Animals , Gryllidae , Humans , Membrane Potentials/physiology , Physical Stimulation , Principal Component Analysis , Sense Organs/cytology , Sensory Receptor Cells/classification , Time Factors
11.
IEEE Trans Biomed Eng ; 57(7): 1757-64, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20176539

ABSTRACT

We describe a flexible multisite microelectrode for insect flight biasing using neural stimulation. The electrode is made of two layers of polyimide (PI) with gold sandwiched in between in a split-ring geometry. The split-ring design in conjunction with the flexibility of the PI allows for a simple insertion process and provides good attachment between the electrode and ventral nerve cord of the insect. Stimulation sites are located at the ends of protruding tips that are circularly distributed inside the split-ring structure. These protruding tips penetrate into the connective tissue surrounding the nerve cord. We have been able to insert the electrode into pupae of the giant sphinx moth Manduca sexta as early as seven days before the adult moth emerges, and we are able to use the multisite electrode to deliver electrical stimuli that evoke multidirectional, graded abdominal motions in both pupae and adult moths. Finally, in loosely tethered flight, we have used stimulation through the flexible microelectrodes to alter the abdominal angle, thus causing the flying moth to deviate to the left or right of its intended path.


Subject(s)
Cybernetics/instrumentation , Electric Stimulation/instrumentation , Flight, Animal/physiology , Manduca/physiology , Pupa/physiology , Animals , Behavior, Animal , Cybernetics/methods , Electric Stimulation/methods , Electrodes, Implanted , Evoked Potentials, Motor/physiology , Manduca/growth & development , Motor Neurons/physiology
12.
J Neurosci ; 25(22): 5323-32, 2005 Jun 01.
Article in English | MEDLINE | ID: mdl-15930380

ABSTRACT

What is the meaning associated with a single action potential in a neural spike train? The answer depends on the way the question is formulated. One general approach toward formulating this question involves estimating the average stimulus waveform preceding spikes in a spike train. Many different algorithms have been used to obtain such estimates, ranging from spike-triggered averaging of stimuli to correlation-based extraction of "stimulus-reconstruction" kernels or spatiotemporal receptive fields. We demonstrate that all of these approaches miscalculate the stimulus feature selectivity of a neuron. Their errors arise from the manner in which the stimulus waveforms are aligned to one another during the calculations. Specifically, the waveform segments are locked to the precise time of spike occurrence, ignoring the intrinsic "jitter" in the stimulus-to-spike latency. We present an algorithm that takes this jitter into account. "Dejittered" estimates of the feature selectivity of a neuron are more accurate (i.e., provide a better estimate of the mean waveform eliciting a spike) and more precise (i.e., have smaller variance around that waveform) than estimates obtained using standard techniques. Moreover, this approach yields an explicit measure of spike-timing precision. We applied this technique to study feature selectivity and spike-timing precision in two types of sensory interneurons in the cricket cercal system. The dejittered estimates of the mean stimulus waveforms preceding spikes were up to three times larger than estimates based on the standard techniques used in previous studies and had power that extended into higher-frequency ranges. Spike timing precision was approximately 5 ms.


Subject(s)
Action Potentials , Interneurons/physiology , Neurons, Afferent/physiology , Algorithms , Animals , Female , Ganglia, Invertebrate/physiology , Gryllidae , In Vitro Techniques , Information Theory , Physical Stimulation , Reaction Time
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