Age‐ and sex‐dependent alterations in primary somatosensory cortex neuronal calcium network dynamics during locomotion

Over the past 30 years, the calcium (Ca(2+)) hypothesis of brain aging has provided clear evidence that hippocampal neuronal Ca(2+) dysregulation is a key biomarker of aging. Age‐dependent Ca(2+)‐mediated changes in intrinsic excitability, synaptic plasticity, and activity have helped identify some of the mechanisms engaged in memory and cognitive decline based on work done mostly at the single‐cell level and in the slice preparation. Recently, our lab identified age‐ and Ca(2+)‐related neuronal network dysregulation in the cortex of the anesthetized animal. Still, investigations in the awake animal are needed to test the generalizability of the Ca(2+) hypothesis of brain aging. Here, we used in vigilo two‐photon imaging in ambulating mice, to image GCaMP8f in the primary somatosensory cortex (S1), during ambulation and at rest. We investigated aging‐ and sex‐related changes in neuronal networks in the C56BL/6J mouse. Following imaging, gait behavior was characterized to test for changes in locomotor stability. During ambulation, in both young adult and aged mice, an increase in network connectivity and synchronicity was noted. An age‐dependent increase in synchronicity was seen in ambulating aged males only. Additionally, females displayed increases in the number of active neurons, Ca(2+) transients, and neuronal activity compared to males, particularly during ambulation. These results suggest S1 Ca(2+) dynamics and network synchronicity are likely contributors of locomotor stability. We believe this work raises awareness of age‐ and sex‐dependent alterations in S1 neuronal networks, perhaps underlying the increase in falls with age.