A network of excitatory neurons within the pre-Bötzinger complex (pre-BötC) of the mammalian brain stem has been found experimentally to generate robust, synchronized population bursts of activity. An experimentally calibrated model for pre-BötC cells yields typical square-wave bursting behavior in the absence of coupling, over a certain parameter range, with quiescence or tonic spiking outside of this range. Previous simulations of this model showed that the introduction of synaptic coupling extends the bursting parameter range significantly and induces complex effects on burst characteristics. In this paper, we use geometric dynamical systems techniques, predominantly a fast/slow decomposition and bifurcation analysis approach, to explain these effects in a two-cell model network. Our analysis yields the novel finding that, over a broad range of synaptic coupling strengths, the network can support two qualitatively distinct forms of synchronized bursting, which we call symmetric and asymmetric bursting, as well as both symmetric and asymmetric tonic spiking. By elucidating the dynamical mechanisms underlying the transitions between these states, we also gain insight into how relevant parameters influence burst duration and interburst intervals. We find that, in the two-cell network with synaptic coupling, the stable family of periodic orbits for the fast subsystem features spike asynchrony within otherwise synchronized bursts and terminates in a saddle-node bifurcation, rather than in a homoclinic bifurcation, over a wide parameter range. As a result, square-wave bursting is replaced by what we call top hat bursting (also known as fold/fold cycle bursting), at least for a broad range of parameter values. Further, spike asynchrony is a key ingredient in shaping the dynamic range of bursting, leading to a significant enhancement in the parameter range over which bursting occurs and an abrupt increase in burst duration as an appropriate parameter is varied.

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We study an excitatory all-to-all coupled network of N spiking neurons with synaptically filtered background noise and slow activity-dependent hyperpolarization currents. Such a system exhibits noise-induced burst oscillations over a range of values of the noise strength (variance) and level of cell excitability. Since both of these quantities depend on the rate of background synaptic inputs, we show how noise can provide a mechanism for increasing the robustness of rhythmic bursting and the range of burst frequencies. By exploiting a separation of time scales we also show how the system dynamics can be reduced to low-dimensional mean field equations in the limit N --> infinity. Analysis of the bifurcation structure of the mean field equations provides insights into the dynamical mechanisms for initiating and terminating the bursts.

Astrocytes are a major cell type in the mammalian brain. They are not electrically excitable, but generate prominent Ca2+ signals related to a wide variety of critical functions. The mechanisms driving these Ca2+ events remain incompletely understood. In this study, we integrate Ca2+ imaging, quantitative data analysis, and mechanistic computational modeling to study the spatial and temporal heterogeneity of cortical astrocyte Ca2+ transients evoked by focal application of ATP in mouse brain slices. Based on experimental results, we tune a single-compartment mathematical model of IP3-dependent Ca2+ responses in astrocytes and use that model to study response heterogeneity. Using information from the experimental data and the underlying bifurcation structure of our mathematical model, we categorize all astrocyte Ca2+ responses into four general types based on their temporal characteristics: Single-Peak, Multi-Peak, Plateau, and Long-Lasting responses. We find that the distribution of experimentally-recorded response types depends on the location within an astrocyte, with somatic responses dominated by Single-Peak (SP) responses and large and small processes generating more Multi-Peak responses. On the other hand, response kinetics differ more between cells and trials than with location within a given astrocyte. We use the computational model to elucidate possible sources of Ca2+ response variability: (1) temporal dynamics of IP3, and (2) relative flux rates through Ca2+ channels and pumps. Our model also predicts the effects of blocking Ca2+ channels/pumps; for example, blocking store-operated Ca2+ (SOC) channels in the model eliminates Plateau and Long-Lasting responses (consistent with previous experimental observations). Finally, we propose that observed differences in response type distributions between astrocyte somas and processes can be attributed to systematic differences in IP3 rise durations and Ca2+ flux rates.

Oscillatory activity in neuronal networks correlates with different behavioral states throughout the nervous system, and the frequency-response characteristics of individual neurons are believed to be critical for network oscillations. Recent in vivo studies suggest that neurons experience periods of high membrane conductance, and that action potentials are often driven by membrane-potential fluctuations in the living animal. To investigate the frequency-response characteristics of CA1 pyramidal neurons in the presence of high conductance and voltage fluctuations, we performed dynamic-clamp experiments in rat hippocampal brain slices. We drove neurons with noisy stimuli that included a sinusoidal component ranging, in different trials, from 0.1 to 500 Hz. In subsequent data analysis, we determined action potential phase-locking profiles with respect to background conductance, average firing rate, and frequency of the sinusoidal component. We found that background conductance and firing rate qualitatively change the phase-locking profiles of CA1 pyramidal neurons vs. frequency. In particular, higher average spiking rates promoted band-pass profiles, and the high-conductance state promoted phase-locking at frequencies well above what would be predicted from changes in the membrane time constant. Mechanistically, spike-rate adaptation and frequency resonance in the spike-generating mechanism are implicated in shaping the different phase-locking profiles. Our results demonstrate that CA1 pyramidal cells can actively change their synchronization properties in response to global changes in activity associated with different behavioral states.