Publications by authors named "Heraldo Memelli"

Hypoglossal motoneurons (HMs) are located in the brainstem and play an important role in the maintenance of upper airway patency. HMs are known to be coupled to one another via gap junctions and exhibit synchronous firing behavior when driven by premotor inputs. In the current study, we used a computational model to analyze the influence of firing frequency on synchronous firing behavior of a network of gap junction-coupled HMs.

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Dendritic morphology constrains brain activity, as it determines first which neuronal circuits are possible and second which dendritic computations can be performed over a neuron's inputs. It is known that a range of chemical cues can influence the final shape of dendrites during development. Here, we investigate the extent to which self-referential influences, cues generated by the neuron itself, might influence morphology.

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In specific regions of the central nervous system (CNS), gap junctions have been shown to participate in neuronal synchrony. Amongst the CNS regions identified, some populations of brainstem motoneurons are known to be coupled by gap junctions. The application of various gap junction blockers to these motoneuron populations, however, has led to mixed results regarding their synchronous firing behavior, with some studies reporting a decrease in synchrony while others surprisingly find an increase in synchrony.

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Most models of central pattern generators (CPGs) involve two distinct nuclei mutually inhibiting one another via synapses. Here, we present a single-nucleus model of biologically realistic Hodgkin-Huxley neurons with random gap junction coupling. Despite no explicit division of neurons into two groups, we observe a spontaneous division of neurons into two distinct firing groups.

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Large-scale models of neuronal structures are needed to explore emergent properties of mammalian brains. Because these models have trillions of synapses, a major problem in their creation is synapse placement. Here we present a novel method for exploiting consistent fiber orientation in a neural tissue to perform a highly efficient modified plane-sweep algorithm, which identifies all regions of 3D overlaps between dendritic and axonal projection fields.

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