“…Both spontaneous and stimulated spiking activities provide unique information on the interactions of ion channels and synapses from single neurons to complex networks 5,6 . For decades, a number of techniques have been developed to record action potentials, including patch-clamps 7,8 , optical-probes 3,9,10 , multi-electrode arrays 6,11,12 , and several types of optical imaging modalities 4,5,10,11 . In particular, single/two-photon fluorescence microscopy has become one of the most powerful and popular approaches to monitoring ion dynamics of neuronal activities in large networks.…”