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J P Segundo

Publications and source records attributed to J P Segundo.

At least 19 recordsLinked to original sources
PubMed1989

Effects of stimulus timing on transmitter release and postsynaptic membrane potential at crayfish neuromuscular junctions.

Different synaptic terminals of the single excitor axon to the opener muscle of crayfish (Procambarus clarkii) often release transmitter in a very different manner when stimulated with the same equal-interval, doublet, or triplet patterns. Compared to synapses that show little facilitation (low Fe synapses), highly facilitating (high Fe) synapses show greater percentage increases in several measures of synaptic efficacy when stimulated with any of these patterns. Low Fe synapses usually show the greater absolute changes in these measures of synaptic efficacy. Changes in the span and pattern of doublets and triplets can independently affect both pre- and postsynaptic measures of synaptic efficacy at either low Fe or high Fe synapses.

Animals↗
PubMed1988

Locking, intermittency, and bifurcations in a periodically driven pacemaker neuron: Poincaré maps and biological implications.

Slowly adapting stretch receptor (SAO) pacemaker neurons, driven with periodic tugs, were analyzed by way of Poincaré mappings (Appendix). Two behaviors were apparent. i) Intermittency characterized previously unclear situations: discharges shifted irregularly between prolonged epochs where spike phases (relative to tugs) and intervals barely changed (slid), and brief bursts with marked variations (skipped). ii) Locking was well-known: phases and intervals remained almost fixed, regardless of the initiation. Changing frequencies, map domains with locking (ordered according to spikes/tugs ratios), alternated with intermittent ones. The best fit for any experimental map was a curve, not straight but certainly unidimensional, continuous and monotonic; it varied characteristically with frequency. This suggested relations called diffeomorphisms, implying periodicity and quasi-periodicity. Outcomes, expanding previous knowledge and meaningful biologically, were i) a precise, exhaustive behavior list (including between behavior transitions) and ii) a thorough understanding or model. This, in turn, provides norms for more specific models (single-variable ones suffice), constraints upon basic mechanisms (one variable, reflecting several real ones combined, should behave as the phase), and forecasts for future experimentation (e.g., unexamined tug frequencies and amplitudes).

Animals↗
PubMed1987

Testing a model of excitatory interactions between oscillators.

The experimentally observed influence of regularly arriving tugs upon the AP discharge of the slowly-adapting stretch receptor organ (SAO) of crayfish was compared to a model of pacemaker excitatory synaptic interactions (Segundo and Kohn 1981). Criteria for compliance referred to facets as A) the excitation, B) the postulates, and C) the behavior. A) Excitation was implied primarily by the tug initially increasing the AP rate (it subsequently decreased it). B) The pacemaker AP discharges, and with more reason the electronically driven tugs, were considered acceptably regular sequence (postulate i). Tugs advanced the next AP (postulate ii); the "delay function" plots of delays vs. phases, i.e. interval shortenings vs. the time from the last AP to the tug, were close to the V of postulate iii, even though the shortest phases tended to postpone the next AP and the longest ones did not trigger immediately but with an around 5 ms latency. These effects were displayed also as "old phase vs. new phase" plots. The interval following that with the tug tended to be lengthened, but the pre-tug timing was not recovered. C) Behavior during a train of excitatory events, both in model and experiments, went through very similar initial settlings and eventual steady-states. The latter were characterized in the model by 1. an average excitatory vs. excited rate display formed by an endless number of segments with all positive rational slopes separated by negative-going discontinuities, 2. locking in the sense of preferential phases, and 3. periodic repetition of the same phases and inter-AP intervals. Experimental results were compatible with this. Such behavior was absent when the tug sequence was highly irregular. The initial settling, in the SAO as in the model, depended jointly on the first phase phi 1 and the intertug interval E. If the former was under lambda, it went through one or two monotonic phase-decreasing stages (one smaller, the other larger, than lambda), or through a single increasing one, depending on E being smaller or greater than, respectively, an estimated but never actually observed E leading to unstable lockings. If the initial phase was greater than lambda, settling with E's under rN + lambda involved jumps between larger than and smaller than lambda phases; with E's over rn + lambda, it involved an intermediate stable locking with phi = E-rN.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1985

Dynamic and static hysteresis in crayfish stretch receptors.

This report calls attention to the magnitude and pervasiveness of hysteresis in the coding from length to afferent discharges in crayfish stretch receptor organs (SRO's). The influence of previous lengths on the rate that corresponded to a particular length L was manifest by a substantial excess of that encountered when L was arrived at from a shorter value over that when arrived at from a longer one. Hysteretic loops were present under dynamic conditions when length was modulated quasi-sinusoidally in the length vs. rate Lissajous plots of both the slowly and the fast-adapting organs (SAO, FAO), either not perturbed or perturbed. Loops became narrower with increasing frequency (except for when 1 to 1 locking appeared, Diez Martínez and Segundo, 1983). Hysteretic loops were present under static conditions when length changes were step-like, and fully adapted rates were noted in the SAO and in the perturbed FAO. Earlier reports suggest that hysteresis reflects jointly at least mechanical and electrogenic factors in the "length-to-local dendritic effects" and in the "generator potential to discharge" stages. Several models, either mechanical or mathematical, reveal hysteretic behavior. Detailed analysis has not been performed except for one instance (Chua and Bass, 1972) where, for example, loop-narrowing at higher frequencies occurs only with certain weighting functions whose physiological significance is as yet obscure. Hysteresis may be more widespread than suspected in sensory (and perhaps other) systems: it involves a multi-valuedness that raises the issue of how central mechanisms infer stimulus magnitude retrospectively from the discharge.

Action Potentials↗
PubMed1979

Empirical examination of the threshold model of neuron firing.

An elementary model of neuronal activity involves temporal and spatial summation of postsynaptic currents that are elicited by presynaptic spikes and that, in turn, elicit postsynaptic potentials at a trigger zone; when the potential at the trigger zone exceeds a "threshold" level, a postsynaptic spike is generated. This paper describes three methods of estimating the "summation function", that is, the function of time that converts the synaptic current into potential at the trigger zone: namely, maximum likelihood, cross-correlation analysis and cross-spectral analysis. All three methods, when applied to input-output data collected on various neurons of Aplysia californica, give comparable results. As estimated, the summation function involved in the explored cells has an early positive-going swing that is large and brief. In the cell L5, but not in R2, there was also a late negative-going swing of longer duration.

Animals↗
PubMed1978

Multivalued stimulus-response relation in isolated elasmobranch utricles.

The relation between a maintained spatial orientation and the corresponding fully adapted discharge rate was multivalued in all the afferents tonically sensitive to maintained spatial orientation observed in isolated utricles of Rhinobates productus. The spread of rate values was of the order of changes produced by natural tilts. The occurrence of multivaluedness in isolated receptors indicated that peripheral issues are sufficient. Two factors contributed: firstly, the side from which the orientation had been reached (i.e. "hysteresis"): higher adapted rates occurred when the preceding orientation was characterized by lower rates and when the corresponding transition caused acceleration; secondly, "spontaneous" rate variations, some of which resembled markedly, and interacted with, the effects of tilts. It was not possible to identify the basic mechanisms underlying these factors. The multivaluedness in the coding of maintained position, because of its constancy and magnitude, cannot be ignored. It, as well as the sensitivity to fast transients, must be taken into account in utricular models, in evaluations of information transmission, and in psychophysical explorations.

Action Potentials↗
PubMed1978

Uncoupling of electrotonic synapses by calcium.

The degree of axo-axonal synaptic coupling between nerve cells in the buccal ganglion of Navanax was investigated in relation to intracellular ionic calcium. Increasing intracellular Ca2+ by injection of Ca2+, injection of Na+, or application of ionophore X537A produced uncoupling after at least 90 min, if metabolic inhibitor was present in the medium. Subsequent removal of the metabolic inhibitor reestablished the coupling in less than 30 min. Injected Sr2+ also mimicked the uncoupling action of Ca2+. The presence of a metabolic inhibitor alone had no effect on the coupling. These results lead to the following conclusions: (i) Uncoupling is due to an increased free Ca2+ concentration at the junctions. (ii) The liberation of endogenous sequestered Ca2+ is not sufficient to produce uncoupling except if an excess Ca2+ had been previously sequestered. The electrical synapses in the buccal ganglion of Navanax thus appear to be affected by Ca2+ in a similar way as gap junctions studied in non-neural tissues.

Animals↗
PubMed1976

Spike initiation by transmembrane current: a white-noise analysis.

1. Those features of a transmembrane current correlated with spike initiation were examined in Aplysia neurones using a Gaussian white-noise stimulus. This stimulus has the advantages that it presents numerous wave forms in random order without prejudgement as to their efficacies, and that it allows straightforward statistical calculations. 2. Stimulation with a repeating segment of Gaussian white-noise current revealed remarkable invariance in the firing times of the tested neurones and indicated a high degree of reliability of their response. 3. Frequencies (less than 5 Hz) involved in spike triggering propagated faithfully for up to several millimetres, justifying intrasomatic current injection to examine spike initiation at the trigger locus. 4. Examination of current wave forms preceding spikes indicated that a wide variety could be effective. Hence, a statistical analysis was performed, including computation of probability densities, averages, standard deviations and correlation coefficients of pairs of current values. Each statistic was displayed as a function of time before the spike. 5. The average current trajectory preceding a spike was multiphasic and depended on the presence and polarity of a d.c. bias. An early relatively small inward- or outward-going phase was followed by a large outward phase before the spike. The early phase tended to oppose the polarity of the d.c. bias. 6. The late outward phase of the average current trajectory reached a maximum 40--75 msec before triggering the action potential (AP) and returned to near zero values at the moment of triggering. The fact that the current peak occurs in advance of the AP may be partially explained by a phase delay between the transmembrane current and potential. The failure of the average current trajectory to return to control values immediately following the peak argues for a positive role of the declining phase in spike triggering. 7. Probability densities preceding spikes were Gaussian, indicating that the average was also the most probable value. Although the densities were broad, confirming that spikes were preceded by a wide variety of current wave forms, their standard deviations were reduced significantly with respect to controls, suggesting preferred status of the average current trajectory in spike triggering. 8. The matrix of correlation coefficients between current pairs suggested that spikes tended to be preceded by wave forms that in part kept close to the average current trajectory and in part preserved its shape. 9. The average first and second derivatives of spike-evoking epochs revealed that current slope and acceleration, respectively, were most crucial in the last 200 msec before spike triggering, and that these dynamic stimulus components were more important for a cell maintained under a depolarizing, rather than a hyperpolarizing bias. 10...

Action Potentials↗
PubMed1975

Response of the elasmobranch utricle to maintained spatial orientation, transitions and jitter.

1. The spike discharges of single first order afferents from the utricle were recorded in the isolated head of the guitarfish and tested for responses to maintained spatial orientation, to transitions and to a small positional jitter representing natural perturbations. Sensitivity to maintained orientation is referred to as "tonic", and to transitions and jitter as "phasic". 2. Most responsive cells were either phasically, or phasically and tonically sensitive. A few were exclusively tonic. Tonic responsiveness implied that maintained orientation was associated with a stationary discharge which differed from one position to another; it sometimes differed also from one station to another at the same position. Transitions from one position to another evoked a rate change that later adapted to the level of the tonic response. Opposite transitions evoked rate changes in the opposite sense. The phasic rate change was usually larger for transitions that increased the rate. Many units were non-responsive. The prevalence of phasic over tonic sensitivity is stressed, and the remarkable heterogeneity of utricular afferents confirms that the macula is not uniform, probably coding a wide variety of head accelerations. 3. The jitter increased the ongoing scatter of intervals and binrates, changing, complicating, or abolishing their periodicity. The jitter could influence the effects of maintained orientation, increasing, decreasing, inverting or even revealing directional sensitivity. It could also force previously independent units into an orientation-dependent correlation; hence, between-cell correlation is potentially useful in coding of spatiel orientation. Naturally occurring perturbations may sonstitute a significant issue of normal operation. 4. Certain afferents from the horizontal semicircular canal showed a slow tonic response to maintained spatial orientation.

Action Potentials↗