Abstract
Twenty-three young adults (4 Females, 25.13 ± 3.72 years) performed an intermittent maximal handgrip force task using their dominant hand for 20 min (3.5 s squeeze/6.5 s release, 120 blocks) with concurrent cortical activity imaging by functional Near-Infrared Spectroscopy (fNRIS; OMM-3000, Shimadzu Corp., 111 channels). Subjects were grouped as physically active (n = 10) or inactive (n = 12) based on a questionnaire (active-exercise at least four times a week, inactive- exercise less than two times a week). We explored how motor task fatigue affected the vasomotion-induced oscillations in ΔHbO as measured by fNIRS at each hemodynamic frequency band: endothelial component (0.003–0.02 Hz) associated to microvascular activity, neurogenic component (0.02–0.04 Hz) related to intrinsic neuronal activity, and myogenic component (0.04–0.15 Hz) linked to activity of smooth muscles of arterioles. To help understand how these three neurovascular regulatory mechanisms relate to handgrip task performance we quantified several dynamic fNIRS metrics, including directional phase transfer entropy (dPTE), a computationally efficient and data-driven method used as a marker of information flow between cortical regions, and directional connectivity (DC), a means to compute directionality of information flow between two cortical regions. The relationship between static functional connectivity (SFC) and functional connectivity variability (FCV) was also explored to understand their mutual dependence for each frequency band in the context of handgrip performance as fatigued increased. Our findings ultimately showed differences between subject groups across all fNIRS metrics and hemodynamic frequency bands. These findings imply that physical activity modulates neurovascular control mechanisms at the endogenic, neurogenic, and myogenic frequency bands resulting in delayed fatigue onset and enhanced performance. The dynamic cortical network metrics quantified in this work for young, healthy subjects provides baseline measurements to guide future work on older individuals and persons with impaired cardiovascular health.
Highlights
Cerebral autoregulation helps maintain a relatively constant oxygen supply to the brain during changes in arterial blood pressure, by maintaining cerebral blood flow (CBF) relatively constant
The brain maintains relatively constant regional CBF through coordinated effort of endogenic, neurogenic and myogenic mechanisms that are known to be active in different hemodynamic frequency bands (Cipolla, 2009; Peterson et al, 2011; Tzeng and Ainslie, 2014; Peri-Okonny et al, 2015)
Our results showed differences between subject groups across all functional near-infrared spectroscopy (fNIRS) metrics and hemodynamic frequency bands, suggesting that active subjects used different cortical activity strategies compared to inactive ones to maintain handgrip performance with increasing fatigue
Summary
Cerebral autoregulation helps maintain a relatively constant oxygen supply to the brain during changes in arterial blood pressure, by maintaining cerebral blood flow (CBF) relatively constant. This occurs via vasoconstriction in response to increased blood pressure and vasodilation in response to decreased blood pressure. There are overlapping regulatory mechanisms of rCBF that have been classified into contiguous ranges of hemodynamic frequencies as endogenic (0.003–0.02 Hz), neurogenic (0.02– 0.04 Hz), and myogenic (0.04–0.15 Hz) (Cipolla, 2009; Li et al, 2012). Regular exercise produces beneficial alterations in the brain that maintain or improve cognition (Bosch et al, 2017; Mueller et al, 2017), and promote motor function (Perrey, 2013), known as exercise-dependent neuroplasticity
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