A 10-min reduction in cerebral blood flow does not alter post-intervention executive function: evidence from lower-body negative pressure
- PMID: 39012475
- DOI: 10.1007/s00221-024-06879-8
A 10-min reduction in cerebral blood flow does not alter post-intervention executive function: evidence from lower-body negative pressure
Abstract
A single bout of exercise as well as exposure to a hypercapnic environment increases cerebral blood flow (CBF) and is an adaptation linked to a post-intervention executive function (EF) benefit. In the present investigation we sought to determine whether a transient reduction in CBF impairs EF. Accordingly, we employed 10-min -30 mmHg and -50 mmHg lower-body negative pressure (LBNP) interventions as well as a non-LBNP control condition. LBNP was employed because it sequesters blood in the lower legs and safely and reliably decreases CBF. Transcranial Doppler ultrasound was used to measure middle cerebral artery velocity (MCAv) to estimate CBF prior to and during LBNP conditions. As well, assessments of the inhibitory control component of EF (i.e., antipointing) were completed prior to (pre-) and immediately after (i.e., post-) each condition. Antipointing requires that an individual reach mirror-symmetrical to an exogenously presented target and is a task providing the resolution to detect subtle EF changes. Results showed that LBNP produced a 14% reduction in MCAv; however, null hypothesis, equivalence and Bayesian contrasts indicated that antipointing metrics did not vary from pre- to post-intervention, and LBNP-based changes in MCAv magnitude were not reliably correlated with antipointing planning times. Hence, a 10-min reduction in CBF did not impact the efficiency or effectiveness of an inhibitory control measure of EF.
© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
References
-
- Ahn B, Sakakibara Y, Paulev P-E, Masuda A, Nishibayashi Y, Nakamura W, Honda Y (1989) Circulatory and respiratory responses to lower body negative pressure in man. Jpn J Physiol 39(6):919–929. https://doi.org/10.2170/jjphysiol.39.919 - DOI - PubMed
-
- Ainslie PN, Duffin J (2009) Integration of cerebrovascular CO 2 reactivity and chemoreflex control of breathing: mechanisms of regulation, measurement, and interpretation. Am J Physiology-Regulatory Integr Comp Physiol 296(5):R1473–R1495. https://doi.org/10.1152/ajpregu.91008.2008 - DOI
-
- Akselrod S, Barak Y, Ben-Dov Y, Keselbrener L, Baharav A (2001) Estimation of autonomic response based on individually determined time axis. Auton Neurosci 90(1–2):13–23. https://doi.org/10.1016/S1566-0702(01)00262-4 - DOI - PubMed
-
- Balldin UI, Krock LP, Hopper NL, Squires WG (1996) Cerebral artery blood flow velocity changes folliwng rapid release of lower body negative pressure. Aviat Space Environ Med 67(1):19–22. https://doi.org/ - PubMed
-
- Barella LA, Etnier JL, Chang Y-K (2010) The immediate and delayed effects of an acute bout of exercise on cognitive performance of healthy older adults. J Aging Phys Act 18(1):87–98. https://doi.org/10.1123/japa.18.1.87 - DOI - PubMed
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