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H J Chiel

Publications and source records attributed to H J Chiel.

26 records · Page 2Linked to original sources

Activity of an identified histaminergic neuron, and its possible role in arousal of feeding behavior in semi-intact Aplysia.

The possible functions of histaminergic neuron C2 were studied in an isolated head preparation from which it was possible to obtain intracellular recordings while the buccal mass exhibited feeding-like responses. Application of food to the lips of the isolated head preparation elicited rhythmic buccal movements that appeared to be ingestion responses, since they moved seaweed into the buccal cavity and towards the esophagus, and their frequency and regularity was similar to the ingestion responses studied in a group of intact animals. The ingestion responses of the buccal mass consisted of 2 main phases of movement of the radula from a middle rest position: forward and return to rest, and backward and return to rest. The relative magnitudes and timing of these 2 phases were variable. Intracellular recordings from C2 in the isolated head revealed that C2 is silent when the buccal mass is quiescent, but that it can be excited into spike activity, either by mechanical stimulation of the perioral zone or by chemostimulation that results in rhythmic movement. C2 fires a burst of spikes in phase with each protraction-retraction cycle, and, if the movements continue, C2 fires even when the eliciting stimulus has been removed. Activity of the cell was usually preceded by fast depolarizing responses that appeared to be blocked axon spikes. The evidence suggests that C2 is part of a positive feedback loop that may help maintain the persistence of arousal of feeding behavior beyond the time that food stimuli are removed.

Animals↗

Sensory function and gating of histaminergic neuron C2 in Aplysia.

This paper explores the possible sensory function of the identified histaminergic neuron C2. Mechanical stimulation of a narrow region around the mouth of the animal (perioral zone) elicits brief depolarizing potentials in C2. Extracellular recordings from the peripheral axons of C2 indicate that the depolarizing potentials are due to action potentials that are conveyed from the periphery but do not invade the cell body, since they fail at a region with a low safety factor within the cerebral ganglion. These blocked axonal spikes (A-spikes) function as if they were excitatory synaptic inputs to C2, since the synaptic output of C2 does not occur unless the A-spikes succeed in evoking full action potentials in the soma (or an electrically close initial segment) of C2. Furthermore, like synaptic potentials, the A-spikes exhibit temporal and spatial summation, and facilitation. C2 receives both tonic and phasic inhibitory synaptic potentials, which can decrease the summation of A-spikes and thereby alter the frequency-filtering properties of C2 or block its synaptic output. Thus, C2 appears to be an unusual proprioceptive afferent that has a high degree of integrative function and may provide critical gating that is dependent on a variety of external and internal conditions.

Animals↗

An identified histaminergic neuron modulates feeding motor circuitry in Aplysia.

An identified histaminergic neuron, C2, in the marine mollusk Aplysia is a complex mechanoafferent which appears to contribute to the maintenance of food arousal by means of its synaptic connections to the metacerebral cell (MCC). Because C2 also has extensive synaptic outputs to neurons other than the MCC, we studied its possible motor functions. We identified several synaptic followers of C2 and found that some were excitatory motor neurons for extrinsic muscles of the buccal mass, while others were modulatory motor neurons that inhibited contractions. In addition, we found that these neurons and other synaptic followers of C2 received powerful inputs during feeding motor programs. In order to determine the functional significance of the synaptic outputs of C2, we studied extrinsic buccal muscles (E4 and E5) whose motor neuron (C6) is excited by C2. Extracellular recordings from these muscles indicated that they receive input during swallowing and rejection, but not during biting movements. Lesions of these muscles, or of all extrinsic muscles, did not prevent animals from feeding, but decreased feeding efficiency, that is, the amount of seaweed an animal could ingest with each swallow. The data suggest that C2 is an integrative proprioceptive cell that functions as a premotor neuron. The non-MCC synaptic outputs of C2 may reinforce the actions of the central feeding motor program. Specifically, C2 appears to aid the functioning of muscles that produce fine adjustments of the buccal mass and contribute to the efficiency of feeding behavior, rather than in producing gross movements.

Animals↗

Short-term variations in diet composition change the pattern of spontaneous motor activity in rats.

The nocturnal activity patterns of rats changed significantly within 3 days after they were given unrestricted access to isocaloric diets in which the ratio of carbohydrate to protein was systematically varied. As the ratio increased, the rats were more continuously active. The subjects showed similar responses to variations in this ratio whether the diet contained 15 or 45 percent fat. No correlation was found between the number of calories an animal ate and its activity pattern.

Animals↗

Suppression of amphetamine-induced hypothermia by the neutral amino acid valine.

Pretreatment with valine (0.5-2.0 mmoles/kg) can suppress the hypothermic response of rats placed in a 4degreesC environment and given d-amphetamine sulfate (5 or 10 mg/kg). The amino acid was most effective when given 30 minutes before amphetamine administration, at which time it also significantly lowered brain tyrosine concentration (and, presumably, suppressed catecholamine synthesis). Because dopaminergic neurons mediate the hypothermic response to amphetamine and because amphetamine's ability to produce hypothermia requires, in part, the release of newly synthesized dopamine, these observed effects of valine pretreatment support the hypothesis that treatments which alter precursor (tyrosine) availability also affect brain catecholamine synthesis.

Animals↗

Evolution and analysis of model CPGs for walking: II. General principles and individual variability.

Are there general principles for pattern generation? We examined this question by analyzing the operation of large populations of evolved model central pattern generators (CPGs) for walking. Three populations of model CPGs were evolved, containing three, four, or five neurons. We identified six general principles. First, locomotion performance increased with the number of interneurons. Second, the top 10 three-, four-, and five-neuron CPGs could be decomposed into dynamical modules, an abstract description developed in a companion article. Third, these dynamical modules were multistable: they could be switched between multiple stable output configurations. Fourth, the rhythmic pattern generated by a CPG could be understood as a closed chain of successive destabilizations of one dynamical module by another. A combinatorial analysis enumerated the possible dynamical modular structures. Fifth, one-dimensional modules were frequently observed and, in some cases, could be assigned specific functional roles. Finally, dynamic dynamical modules, in which the modular structure itself changed over one cycle, were frequently observed. The existence of these general principles despite significant variability in both patterns of connectivity and neural parameters was explained by degeneracy in the maps from neural parameters to neural dynamics to behavior to fitness. An analysis of the biomechanical properties of the model body was essential for relating neural activity to behavior. Our studies of evolved model circuits suggest that, in the absence of other constraints, there is no compelling reason to expect neural circuits to be functionally decomposable as the number of interneurons increase. Analyzing idealized model pattern generators may be an effective methodology for gaining insights into the operation of biological pattern generators.

Algorithms↗

Evolution and analysis of model CPGs for walking: I. Dynamical modules.

Can one develop an abstract description of the dynamics of pattern generators that provides quantitative insight into their operation? We explored this question by examining the dynamics of a model central pattern generator that was created using an evolutionary algorithm. We propose an abstract description based on the concept of a dynamical module, a set of neurons that simultaneously make their transitions from one quasistable state to another while the synaptic inputs that they receive from other neurons remain essentially constant, thus temporarily reducing the dimensionality of the circuit dynamics. Using the mathematical tools of dynamical systems theory, we describe a method for identifying dynamical modules and demonstrate that this concept can be used to quantitatively characterize constraints on neural architecture, account for phase durations, and predict the effects of parameter changes. Moreover, this abstract description reveals coordinated parameter changes that leave the overall circuit dynamics essentially unchanged. In a companion article we employ this abstract description to examine the relationship between general principles and individual variability in large populations of evolved model pattern generators.

Gait↗