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Ashhad, S.

Publications and source records attributed to Ashhad, S..

2 recordsLinked to original sources

Microcircuit synchronization and heavy tailed synaptic weight distribution in preBötzinger Complex contribute to generation of breathing rhythm

The preBotzinger Complex, the mammalian inspiratory rhythm generator, encodes inspiratory time as motor pattern. Spike synchronization throughout this sparsely connected network generates inspiratory bursts albeit with variable latencies after preinspiratory activity onset in each breathing cycle. Using preBotC rhythmogenic microcircuit minimal models, we examined the variability in probability and latency to burst, mimicking experiments. Among various physiologically plausible graphs of 1000 point neurons with experimentally determined neuronal and synaptic parameters, directed Erd[o]s-Renyi graphs best captured the experimentally observed dynamics. Mechanistically, preBotC (de)synchronization and oscillatory dynamics are regulated by the efferent connectivity of spiking neurons that gates the amplification of modest preinspiratory activity through input convergence. Furthermore, to replicate experiments, a lognormal distribution of synaptic weights was necessary to augment the efficacy of convergent coincident inputs. These mechanisms enable exceptionally robust yet flexible preBotC attractor dynamics that, we postulate, represent universal temporal-processing and decision-making computational motifs throughout the brain.

neuroscience↗

Network Synchronization and Synchrony Propagation:Emergent Elements of Inspiration

The preBotzinger Complex (preBotC) - the kernel of breathing rhythmogenesis in mammals - is a non-canonical central pattern generator with undetermined mechanisms. We assessed preBotC network dynamics under respiratory rhythmic and nonrhythmic conditions in vitro. In each cycle under rhythmic conditions, an inspiratory burst emerges as (presumptive) preBotC rhythmogenic neurons transition from aperiodic uncorrelated population spike activity to become increasingly synchronized during preinspiration, triggering bursts; burst activity subsides and the cycle repeats. In a brainstem slice in nonrhythmic conditions, antagonizing GABAA receptors can initiate this periodic synchronization and consequent rhythm coincident with inducing a higher conductance state in nonrhythmogenic preBotC output neurons. Furthermore, when input synchrony onto these neurons was weak, preBotC activity failed to propagate to motor nerves. Our analyses uncover a dynamic reorganization of preBotC network activity - underpinning intricate cyclic neuronal interactions leading to network synchronization and its efficient propagation - correlated with and, we postulate, essential to, rhythmicity.

neuroscience↗