Why the study?
How do arterial blood pressure, PaCO2, and neural activation stimulus contribute to changes in cerebral blood flow velocities during active, passive, and motor imagery paradigms?
How do arterial blood pressure, PaCO2, and neural activation stimulus contribute to changes in cerebral blood flow velocities during active, passive, and motor imagery paradigms?
Separating neural activation from peripheral covariates like blood pressure reveals significant differences in cerebral blood flow responses between motor-cognitive paradigms, highlighting the risk of inaccurate neurovascular coupling assessment if covariates are ignored.
BP adjustment may avert inaccurate neurovascular coupling assessment in motor tasks; leaves open distinct neural contributions across paradigms.
The association between neural activity and cerebral blood flow (CBF) has been used to assess neurovascular coupling (NVC) in health and diseases states, but little attention has been given to the contribution of simultaneous changes in peripheral covariates. We used an innovative approach to assess the contributions of arterial blood pressure (BP), PaCO2, and the stimulus itself to changes in CBF velocities (CBFv) during active (MA), passive (MP), and motor imagery (MI) paradigms. Continuous recordings of CBFv, beat-to-beat BP, heart rate, and breath-by-breath end-tidal CO2 (EtCO2) were performed in 17 right-handed subjects before, during, and after motor-cognitive paradigms performed with the right arm. A multivariate autoregressive-moving average model was used to calculate the separate contributions of BP, EtCO2, and the neural activation stimulus (represented by a metronome on-off signal) to the CBFv response during paradigms. Differences were found in the bilateral CBFv responses to MI compared with MA and MP, due to the contributions of stimulation (P < 0.05). BP was the dominant contributor to the initial peaked CBFv response in all paradigms with no significant differences between paradigms, while the contribution of the stimulus explained the plateau phase and extended duration of the CBFv responses. Separating the neural activation contribution from the influences of other covariates, it was possible to detect differences between three paradigms often used to assess disease-related NVC. Apparently similar CBFv responses to different motor-cognitive paradigms can be misleading due to the contributions from peripheral covariates and could lead to inaccurate assessment of NVC, particularly during MI.
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Salinet et al. (2013) studied this question.
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