Biomedical subjects

A E Dityatev

Publications and source records attributed to A E Dityatev.

11 recordsLinked to original sources

PubMed2001

Structural and physiological properties of connections between individual reticulospinal axons and lumbar motoneurons of the frog.

Although the direct, monosynaptic influence of brainstem projections onto motoneurons is well-known, detailed morphological studies on the synaptic contact systems and a correlation with their functional properties are largely lacking. In this work, 43 pairs, each formed by a reticulospinal fiber contacting a lumbar motoneuron, were identified and studied electrophysiologically. Four of these were successfully labeled intracellularly with horseradish peroxidase (HRP) or neurobiotin and reconstructed using a computer-assisted camera lucida with high resolution. The mean amplitude of excitatory post-synaptic potentials (EPSPs) recorded in these four pairs varied from 100 to 730 microV, spanning most of the range obtained for all pairs (70-1,200 microV; mean +/- SD: 400 +/- 250 microV). Between two and four collaterals of reticulospinal axons established 4-19 close appositions with a labeled motoneuron. Mean distance from the origin of each collateral to any bouton on that collateral was 566-817 microm. A presynaptic action potential must pass 11 branch points on average to reach it. Similarly, the boutons presumably contacting motoneurons were on average 558-624 microm (9-11 branch points) from the origin of the collateral. The distributions of diameters of all boutons and those making putative contacts with stained motoneurons were very similar. The dendritic surface of stained motoneurons was symmetrically distributed along the rostrocaudal axis with more than half the surface being more than 500 microm from the soma. However, the contacts from reticulospinal axons were concentrated ventromedially, 262-356 microm (range of average values for four connections) from the motoneuron soma, in some instances on very proximal dendritic segments. Thus, the location and size of putative contacts in relation to axonal collaterals was not distinguishable from location and size of other boutons, but they occupied specific positions on dendrites of lumbar motoneurons. The number of contacts formed by a reticulospinal axon on a motoneuron in a particular location could be described as the product of the available dendritic surface and the total number of presynaptic boutons in this region. Compartmental models of the reconstructed motoneurons were created, and currents with the time course of an alpha function were injected at the sites of these putative contacts. Despite the restricted volume occupied by contacts from a single fiber, a high variability of their contributions to somatic EPSPs owing to electrotonic attenuation was shown: The coefficient of variation of quantal responses was estimated to be between 60% and 120%, comparable to the variability of the path distance between contacts and soma (50-90%).

Animals↗

PubMed1998

Transient activity of excitatory Cl- channels in Chara: evidence for quantal release of a gating factor.

In attached patches on the plasma membrane of nonexcited Chara corallina cells, randomly activating, transient Cl- currents with variable amplitudes were recorded. The peak amplitudes of these currents could be grouped into distinct populations with approximately equidistant mean peak currents. Generally, the mean current of the smallest population measured about half of the distance between the means of subsequent populations. Currents of the smallest population occurred most frequently at all voltages; the frequency of observations decreased with increasing amplitudes of the currents. At all voltages transient currents from different populations were similar in duration with the exception of the smallest currents, which lasted only 0.6 times as long as larger currents. Furthermore, transient currents were most frequent at positive voltages, but once initiated at a positive conditioning pulse they were also observed during subsequent pulses to negative voltages. The results are consistent with the idea that Chara contains Ca2+ stores in the vicinity of the plasma membrane, which are indirectly filled from the external medium. Upon quantal Ca2+ discharge from adjacent stores, a process independent of membrane voltage, the concentration of Ca2+ in the cytoplasm increases transiently. Depending on the number of discharging stores, distinct numbers of Ca2+-stimulated Cl- channels activate, giving rise to the macroscopic excitatory Cl- current in these cells.

Biological Transport↗

PubMed1998

Synaptic differentiation of single descending fibers studied by triple intracellular recording in the frog spinal cord.

Evoked excitatory postsynaptic potentials (EPSPs) were simultaneously intracellularly recorded in two lumbar motoneurons located in spinal segments 8-10 in response to intraaxonal stimulation of a descending fiber. Their mean amplitudes, paired-pulse facilitation, and short- and long-term posttetanic potentiation were compared to reveal possible functional differences among synapses formed by one axon on different postsynaptic targets. The mean amplitudes of EPSPs recorded in two motoneurons were significantly different in most experiments. This amplitude difference was related to the location of motoneurons in that it was twofold larger in motoneurons separated by >1 mm than in motoneurons located within 200 micron m of one another and also that the amplitude of EPSPs recorded in motoneurons located in the tenth segment was regularly smaller than the amplitude recorded in the ninth segment. The estimation of binomial model parameters suggests that the difference in mean EPSP amplitude was due mostly to differences in the maximal number of quanta prepared for release (binomial parameter N) and in mean release probability rather than to differences in quantal size. The ability of connections formed by a single axon on different motoneurons to undergo use-dependent synaptic modulations was different on scales of milliseconds, seconds, and tens of minutes as revealed by the measurements of effects of paired-pulse and tetanic stimulation. The difference in magnitude of short-term posttetanic potentiation in connections formed by a single descending axon was significantly correlated with the difference in mean probability of release in these connections. Thus our data revealed a functional nonuniformity of synapses formed by individual descending fibers on widely separated motoneurons, most likely innervating different muscles. This process can be one of the mechanisms by which a fine descending control of recruitment of motoneuronal populations is achieved.

Animals↗

PubMed1997

Natural variability in the number of dendritic segments: model-based inferences about branching during neurite outgrowth.

A study was made of the possible basis for naturally occurring variations in the number of segments in individual dendritic trees. Distributions of the number of terminal segments have been studied in dendrites from rat, cat, and frog motoneurons, basal dendrites from rat visual cortex pyramidal and non-pyramidal neurons, in rat cerebellar Purkinje cell dendritic trees, and in human hippocampal dentate granule cells. By means of a mathematical model for dendritic branching, it was shown that the variation in the number of dendritic segments can be accounted for by assuming that new branches during neurite outgrowth are formed randomly at terminal segments. The observed terminal segment number distributions could be closely approximated by additionally assuming that branching probabilities decline with increasing number of terminal segments in growing dendrites. The pyramidal neuron group differed significantly from the other neuron groups in such a way as to suggest that this decline is stronger than in the dendrites of other types of neurons. By using literature data on the mean number of terminal segments in rat cerebellar Purkinje cells, measured at different times during early development, an estimate could be obtained of the time-course of the branching probabilities. The branching probability of a terminal segment was found to be in the order of 0.002 per hour in the first 4 weeks postnatal with a 5-fold transient increase in the second week.

Animals↗

PubMed1996

Reliability of spike propagation in arborizations of dorsal root fibers studied by analysis of postsynaptic potentials mediated by electrotonic coupling in the frog spinal cord.

1. Postsynaptic potentials were recorded in lumbar motoneurons of the frog in response to electrical activation of dorsal roots. After chemical synaptic transmission was blocked by replacing Ca2+ with Mg2+ in the superfusion medium, it was confirmed that the remaining electrical excitatory postsynaptic potentials (EEPSPs) recorded in motoneurons consisted of potential changes-produced by electrical coupling between the motoneurons and the stimulated axons. The EEPSPs could then be used as an assay to study the reliability of spike propagation into presynaptic terminals. 2. EEPSPs typically consisted of three components. The first was a small positive deflection (prespike or presynaptic volley) that could also be recorded extracellularly. The second component was a spikelike fast positive component and the third was a slow positive component that followed the second but had a distinct maximum and a slow decay. The amplitude of the fast component did not correlate with that of either the prespike or the slow component. 3. 4-Aminopyridine (0.1 mM), which widens action potentials by blocking K+ channels, increased the amplitude and width of EEPSPs. Heptanol (1-4 mM), which is known to be a blocker of electrical coupling, could block EEPSPs. 4. The amplitudes of EEPSPs evoked by dorsal root stimulation were compared at different temperatures (7.5-19.5 degrees C). A slight decrease of the amplitude of the fast component with increasing temperature (Q10 = 0.8) was within limits predicted by resistance-capacitance filtering of the presynaptic spike at the different temperatures, suggesting that the temperature does not affect propagation of the spike in this synapse. 5. The amplitude of the fast component of EEPSPs evoked by single-pulse and paired-pulse stimulation did not fluctuate more than the baseline noise in 37 experiments in which the SD of baseline noise was < 100 microV. We conclude that electrical synaptic transmission does not fluctuate intermittently in this system, and that branch points conduct or fail to conduct for periods of time longer than the longest period in the analyzed experiments.

Animals↗

PubMed1995

Comparison of the topology and growth rules of motoneuronal dendrites.

The complexity, shape, and branching modes of the dendrites of spinal motoneurons were compared in cat, rat, and frog using topological analysis and growth models. The complexity of motoneuronal dendrites, measured as the mean number of terminal segments, varied significantly among samples and was related to contractile properties of innervated motor units. Despite this variation, all mature motoneurons having a mean number of terminal segments per dendrite greater than ten (up to 24.3) exhibited a narrow range of values of coefficients describing the symmetry of tree shapes (0.42-0.47). This implies low variability in the topological shape of motoneuronal dendrites of different animals. This similarity of tree shapes proved to be a result of the similarity of growth rules. The growth of the dendrites could be described to a first approximation by a two-parameter (Q and S) model called the QS model and by a multitype Markovian model. The estimation of parameters of the QS model, in which parameter Q is related to the probability of branching of intermediate segments, revealed that Q was equal or close to 0, implying that branching of dendrites is restricted to terminal segments. The estimates of the parameter S, which describes whether the probability of branching increases (S < 0) or decreases (S > 0) exponentially with segment order, were positive. This was in agreement with the results of estimation of probabilities of branching provided by the Markovian model, which showed that the branching probabilities decreased with segment order in an exponential manner in most of the neurons studied. The QS and Markovian models involve different assumptions about the sequence and timing of branching events, and selection of the best model can provide insight into details of dendritic outgrowth. Extensive simulation of tree outgrowth using a Markovian model revealed significant differences between stimulated trees and real dendrites, particularly with regard to variability of the number of terminals and to symmetry. In contrast, the QS model provided a good fit to the mean values and standard deviations of basic topological parameters. This model is adequate to describe the shape of mature motoneuronal dendrites. It implies that dendritic branches have many opportunities to bifurcate during the whole time of development and that bifurcating potency of a branch is a function of the number and position of other branches of that dendrite. Combined with analysis of metrical properties such as lengths of segments, the QS model can assist in a quantitative analysis of development and plasticity.

Animals↗

PubMed1994

Quantal analysis based on spectral methods.

A method for calculating quantal size based on spectral analysis of postsynaptic potential (PSP) amplitude distributions was developed and tested by Monte-Carlo techniques. It was combined with a test to reveal the bias of the estimate of quantal size and to determine whether the peaks in amplitude distributions reflect quantal release or a sampling artifact. Spectral density was computed using fast Fourier transformation after subtraction of a fitted polynomial from the probability density function. The method overestimated quantal size for values less than two standard deviations of noise, indicating that those estimates as well as estimates of quantal size computed for examples of non-quantal distributions are not reliable. This was the case for 34 of 36 sets of sensorimotor excitatory PSPs of the frog, suggesting that most values of the quanta in synapses between primary fibres and lumbar motoneurons are smaller than 70-90 microV.

Animals↗

PubMed1993

Limits of quantal analysis reliability: quantal and unimodal constraints and setting of confidence intervals for quantal size.

An accurate objective method for determining the reliability of estimates of quantal size (Q) at central synapses was developed. To do this, distributions of amplitudes of postsynaptic responses were simulated by convolving a number of discrete amplitudes separated by equal increments Q with gaussian noise, after which the value of Q was estimated by the maximum likelihood method under different constraints on the discrete distribution. It was shown that the likelihood function (LF) had several local maxima under the quantal constraint, and, if the value of the ratio between Q and the standard deviation of the noise (sigma) was less than 3, the global maximum of the LF corresponded to a biased estimate of Q lying in a range of values less than 1.5 sigma. The best estimates of Q were obtained when unimodal discrete distributions of amplitudes resulting from the maximum likelihood method were selected. However, this method also gave biased estimates when Q/sigma was less than 1.5-2.3. The limit of reliability depended on the number of discrete components and the sample size. To calculate confidence intervals for the quantal size, different numbers and weights of components were used to simulate amplitude histograms with different values of Q/sigma. Three data sets were used to illustrate the procedure.

Animals↗

PubMed1992

Modeling of the quantal release at interneuronal synapses: analysis of permissible values of model moments.

A theoretical study of effects of the different factors on fluctuation of post-synaptic potential (PSP) amplitudes was undertaken, using computation of regions of permissible values (RPV) of the ratio between the variance and the mean number of the quanta released (R1) and the ratio between the third moment and the variance (R2). The RPVs of these indexes for the binomial model were compared with regions determined for a number of models incorporating several factors. It has been shown that the involvement of temporal non-uniformity of transmitter release probability, decremental spreading of potentials along dendrites, and failure of spike propagation give the values of skewness index R2 less, compared to the binomial model. Simultaneously, a number of other factors, especially spatial non-uniformity of release probabilities in single release sites, would give amplitude histograms with high positive values of the index. The values of R1 and R2, calculated for 21 samples of sensorimotor EPSP amplitudes, were biased from RPV of these parameters constructed for the binomial model. The scattergram of R1 and R2 can be explained by the presence of two kinds of contacts which release quantum with different probabilities. The same was true for the beta-model based on the assumption that probabilities of quantal release are a sample of values of random variable that has beta-distribution. From analysis of the distribution of individual release probabilities, obtained from evaluation of beta-model parameters, is concluded that a greater part of boutons in the sensorimotor synapses release transmitter with very low probabilities, there being, however, a few boutons with probabilities close to 1.

Animals↗

PubMed1991

Physicochemical properties of signal receptor domains as the basis for sequence comparison.

1. An algorithm of sequence comparison based on average bulkiness of amino acids in protein domains and not requiring sequence alignment is described. 2. A complete evolutionary tree of the signal receptor proteins is built. The STE2 proteins are shown to belong to this family. 3. Factorial analysis of average bulkiness makes it possible to discriminate functional and intraspecies differences between proteins.

Algorithms↗

PubMedDate not supplied

Ligand-receptor interactions. Multidimensional mathematical method of analysis.

The paper embraces information about the character of interaction between pharmacologically active ligands and 11 G-protein-dependent receptors of neurotransmitters. The data are analyzed by the methods of correlation and cluster analyses and of main components. An essential pharmacological affinity is revealed to exist between the receptors which regulate an inhibitory link of the adenylate cyclase system and receptors which activate Ca(2+)-mobilizing polyphosphoinositide system of secondary transmitters. Receptors which activate adenylate cyclase are rather different pharmacologically from two previous groups. Interrelation between the structure and physico-chemical properties of binding sites on receptors and efficiency of their interaction with ligand is discussed.

Adenylyl Cyclases↗