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Malyshev, A.

Publications and source records attributed to Malyshev, A..

3 recordsLinked to original sources

Altered heterosynaptic plasticity impairs visual discrimination learning in adenosine A1 receptor knockout mice

Theoretical and modeling studies demonstrate that heterosynaptic plasticity - changes at synapses inactive during induction - facilitates fine-grained discriminative learning in Hebbian-type systems, and helps to achieve a robust ability for repetitive learning. A dearth of tools for selective manipulation has hindered experimental analysis of the proposed role of heterosynaptic plasticity in behavior. Here we circumvent this obstacle by testing specific predictions about changes in heterosynaptic plasticity, and associated behavioral consequences, following experimental manipulation of adenosine A1 receptors (A1R). We show that, compared to wild-type controls, A1R-knockout mice have impaired synaptic plasticity in visual cortex neurons, coupled with significant deficits in visual discrimination learning. Deficits in A1R-knockouts were seen specifically during re-learning, becoming progressively more apparent with learning on sequential visual discrimination tasks of increasing complexity. These behavioral results confirm our model predictions, and provide the first experimental evidence for a proposed role of heterosynaptic plasticity in learning. HighlightsO_LISynaptic plasticity is impaired in visual cortex neurons in adenosine A1R knockout mice C_LIO_LIHomosynaptic and heterosynaptic plasticity in A1R KO mice is dominated by depression C_LIO_LILearning on sequential, increasingly complex visual tasks is impaired in A1R KO mice C_LIO_LILearning deficits match predicted effects of impaired heterosynaptic plasticity C_LI

neuroscience↗

Action Potentials and Na+ voltage-gated ion channels in Placozoa

Placozoa are small disc-shaped animals, representing the simplest known, possibly ancestral, organization of free-living animals. With only six morphological distinct cell types, without any recognized neurons or muscle, placozoans exhibit fast effector reactions and complex behaviors. However, little is known about electrogenic mechanisms in these animals. Here, we showed the presence of rapid action potentials in four species of placozoans (Trichoplax adhaerens [H1 haplotype], Trichoplax sp.[H2], Hoilungia hongkongensis [H13], and Hoilungia sp. [H4]). These action potentials are sodium-dependent and can be inducible. The molecular analysis suggests the presence of 5-7 different types of voltage-gated sodium channels, which showed substantial evolutionary radiation compared to many other metazoans. Such unexpected diversity of sodium channels in early-branched animal lineages reflect both duplication events and parallel evolution of unique behavioral integration in these nerveless animals. HighlightsO_LIPlacozoans are the simplest known animals without recognized neurons and muscles C_LIO_LIWith only six morphological cell types, placozoans showed complex & rapid behaviors C_LIO_LISodium-dependent action potentials have been discovered in intact animals C_LIO_LIVoltage-gated sodium channels (Nav) in Placozoa support a rapid behavioral integration C_LIO_LIPlacozoans have more Nav channels that any studied invertebrate animal so far C_LIO_LIDiversification of Nav-channels highlight the unique evolution of these nerveless animals C_LI O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=157 SRC="FIGDIR/small/243113v2_ufig1.gif" ALT="Figure 1"> View larger version (52K): org.highwire.dtl.DTLVardef@4d9c5forg.highwire.dtl.DTLVardef@15539bforg.highwire.dtl.DTLVardef@4246faorg.highwire.dtl.DTLVardef@141e5fe_HPS_FORMAT_FIGEXP M_FIG C_FIG

evolutionary biology↗

Estimating short-term synaptic plasticity from pre- and postsynaptic spiking

Short-term synaptic plasticity (STP) critically affects the processing of information in neuronal circuits by reversibly changing the effective strength of connections between neurons on time scales from milliseconds to a few seconds. STP is traditionally studied using intracellular recordings of postsynaptic potentials or currents evoked by presynaptic spikes. However, STP also affects the statistics of postsynaptic spikes. Here we present two model-based approaches for estimating synaptic weights and short-term plasticity from pre- and postsynaptic spike observations alone. We extend a generalized linear model (GLM) that predicts postsynaptic spiking as a function of the observed pre- and postsynaptic spikes and allow the connection strength (coupling term in the GLM) to vary as a function of time based on the history of presynaptic spikes. Our first model assumes that STP follows a Tsodyks-Markram description of vesicle depletion and recovery. In a second model, we introduce a functional description of STP where we estimate the coupling term as a biophysically unrestrained function of the presynaptic inter-spike intervals. To validate the models, we test the accuracy of STP estimation using the spiking of pre- and postsynaptic neurons with known synaptic dynamics. We first test our models using the responses of layer 2/3 pyramidal neurons to simulated presynaptic input with different types of STP, and then use simulated spike trains to examine the effects of spike-frequency adaptation, stochastic vesicle release, spike sorting errors, and common input. We find that, using only spike observations, both model-based methods can accurately reconstruct the time-varying synaptic weights of presynaptic inputs for different types of STP. Our models also capture the differences in postsynaptic spike responses to presynaptic spikes following short vs long inter-spike intervals, similar to results reported for thalamocortical connections. These models may thus be useful tools for characterizing short-term plasticity from multi-electrode spike recordings in vivo.\n\nAuthor SummaryInformation processing in the nervous system critically depends on dynamic changes in the strength of connections between neurons. Short-term synaptic plasticity (STP), changes that occur on timescales from milliseconds to a few seconds, is thought to play a role in tasks such as speech recognition, motion detection, and working memory. Although intracellular recordings in slices of neural tissue have identified synaptic mechanisms of STP and have demonstrated its potential role in information processing, studying STP in intact animals, especially during behavior, is experimentally difficult. Unlike intracellular recordings, extracellular spiking of hundreds of neurons simultaneously can be recorded even in behaving animals. Here we developed two models that allow estimation of STP from extracellular spike recordings. We validate these models using results from in vitro experiments which simulate a realistic synaptic input from a population of presynaptic neurons with defined STP rules. Our results show that both new models can accurately recover the synaptic dynamics underlying spiking. These new methods will allow us to study STP using extracellular recordings, and therefore on a much larger scale than previously possible in behaving animals.

neuroscience↗