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Brain aging is characterized by changes in both hemodynamic and neuronal responses, which may be influenced by the cardiorespiratory fitness of the individual. To investigate the relationship between neuronal and hemodynamic changes, we studied the brain activity elicited by visual stimulation (checkerboard reversals at different frequencies) in younger adults and in older adults varying in physical fitness. Four functional brain measures were used to compare neuronal and hemodynamic responses obtained from BA17: two reflecting neuronal activity (the event-related optical signal, EROS, and the C1 response of the ERP), and two reflecting functional hemodynamic changes (functional magnetic resonance imaging, fMRI, and near-infrared spectroscopy, NIRS). The results indicated that both younger and older adults exhibited a quadratic relationship between neuronal and hemodynamic effects, with reduced increases of the hemodynamic response at high levels of neuronal activity. Although older adults showed reduced activation, similar neurovascular coupling functions were observed in the two age groups when fMRI and deoxy-hemoglobin measures were used. However, the coupling between oxy- and deoxy-hemoglobin changes decreased with age and increased with increasing fitness. These data indicate that departures from linearity in neurovascular coupling may be present when using hemodynamic measures to study neuronal function.

Fast optical signals can be used to study the time course of neuronal activity in localized cortical areas. The first report of such signals [Gratton, G., Corballis, P. M., Cho, E., Fabiani, M., Hood, D., 1995a. Shades of gray matter: Noninvasive optical images of human brain responses during visual stimulation. Psychophysiol, 32, 505-509.] was based on photon delay measures. Subsequently, other laboratories have also measured fast optical signals, but a debate still exists about how these signals are generated and optimally recorded. Here we report data from a visual stimulation paradigm in which different parameters (continuous: DC intensity; modulated: AC intensity and photon delay), wavelengths (shorter and longer than the hemoglobin isosbestic point), and source-detector distances (shorter and longer than 22.5 mm) were used to record fast signals. Results indicate that a localized fast signal (peak latency=80 ms) can be detected with both delay and AC intensity measures in visual cortex, but not with unmodulated DC measures. This is likely due to the fact that differential measures (delay and AC intensity) are less sensitive to superficial noise sources, which heavily influence DC intensity. The fast effect had similar sign at wavelengths shorter and longer than the hemoglobin isosbestic point, consistent with light scattering but not rapid deoxygenation accounts of this phenomenon. Finally, the fast signal was only measured at source-detector distances greater than 22.5 mm, consistent with the intracranial origin of the signal, and providing indications about the minimum distance for recording. These data address some of the open questions in the field and provide indications about the optimal recording methods for fast optical signals.