The functional role of astrocyte calcium signaling in brain information processing was intensely debated in recent decades. This interest was motivated by high resolution imaging techniques showing highly developed structure of distal astrocyte processes. Another point was the evidence of bi-directional astrocytic regulation of neuronal activity. To analyze the effects of interplay of calcium signals in processes and in soma mediating correlations between local signals and the cell-level response of the astrocyte we proposed spatially extended model of the astrocyte calcium dynamics. Specifically, we investigated how spatiotemporal properties of Ca²⁺ dynamics in spatially extended astrocyte model can coordinate (e.g., synchronize) networks of neurons and synapses.

Biological neuronal networks are highly adaptive and plastic. For instance, spike-timing-dependent plasticity (STDP) is a core mechanism which adapts the synaptic strengths based on the relative timing of pre- and postsynaptic spikes. In various fields of physiology, time delays cause a plethora of biologically relevant dynamical phenomena. However, time delays increase the complexity of model systems together with the computational and theoretical analysis burden. Accordingly, in computational neuronal network studies propagation delays were often neglected. As a downside, a classic STDP rule in oscillatory neurons without propagation delays is unable to give rise to bidirectional synaptic couplings, i.e., loops or uncoupled states. This is at variance with basic experimental results. In this mini review, we focus on recent theoretical studies focusing on how things change in the presence of propagation delays. Realistic propagation delays may lead to the emergence of neuronal activity and synaptic connectivity patterns, which cannot be captured by classic STDP models. In fact, propagation delays determine the inventory of attractor states and shape their basins of attractions. The results reviewed here enable to overcome fundamental discrepancies between theory and experiments. Furthermore, these findings are relevant for the development of therapeutic brain stimulation techniques aiming at shifting the diseased brain to more favorable attractor states.

For both the acquisition of mobile electrocardiogram (ECG) devices and early warning and diagnosis of clinical work, high-quality ECG signals is particularly important. We describe an effective system which could be deployed as a stand-alone signal quality assessment algorithm for vetting the quality of ECG signals. The proposed ECG quality assessment method is based on the simple heuristic fusion and fuzzy comprehensive evaluation of the SQIs. This method includes two modules, i.e., the quantification and extraction of Signal Quality Indexes (SQIs) for different features, intelligent assessment and classification. First, simple heuristic fusion is executed to extract SQIs and determine the following SQIs: R peak detection match qSQI, QRS wave power spectrum distribution pSQI, kurtosis kSQI, and baseline relative power basSQI. Then, combined with Cauchy distribution, rectangular distribution and trapezoidal distribution, the membership function of SQIs was quantified, and the fuzzy vector was established. The bounded operator was selected for fuzzy synthesis, and the weighted membership function was used to perform the assessment and classification. The performance of the proposed method was tested on the database from Physionet ECG database, with an accuracy (Acc) of 97.67%, sensitivity (Se) of 96.33% and specificity (Sp) of 98.33% on the training set. Testing against the test datasets resulted in scores of 94.67, 90.33, and 93.00%, respectively. There's no gold standard exists for determining the quality of ECGs. However, the proposed algorithm discriminates between high- and poor-quality ECGs, which could aid in ECG acquisition for mobile ECG devices, early clinical diagnosis and early warning.