Please use this identifier to cite or link to this item: http://hdl.handle.net/1880/51121
Title: Studying cerebral hemodynamics and metabolism using simultaneous near-infrared spectroscopy and transcranial Doppler ultrasound: a hyperventilation and caffeine study
Authors: Yang, Runze
Brugniaux, Julien
Dhaliwal, Harinder
Beaudin, Andrew
Eliasziw, Misha
Poulin, Marc
Dunn, Jeff F.
Keywords: brain;near-infrared spectroscopy;transcranial Doppler ultrasound
Issue Date: 25-Mar-2015
Publisher: Wiley-Blackwell on behalf of The Physiological Society and the American Physiological Society
Citation: Yang, R., J. Brugniaux, H. Dhaliwal, A. E. Beaudin, M. Eliasziw, M. J. Poulin and J. F. Dunn. (2015). Studying cerebral hemodynamics and metabolism using simultaneous near-infrared spectroscopy and transcranial Doppler ultrasound: a hyperventilation and caffeine study. Physiol Rep. 3(4).
Series/Report no.: Physiological Reports;
Abstract: Caffeine is one of the most widely consumed psycho-stimulants in the world, yet little is known about its effects on brain oxygenation and metabolism. Using a double-blind, placebo-controlled, randomized cross-over study design, we combined transcranial Doppler ultrasound (TCD) and near-infrared spectroscopy (NIRS) to study caffeine's effect on middle cerebral artery peak blood flow velocity (Vp), brain tissue oxygenation (StO2), total hemoglobin (tHb), and cerebral oxygen metabolism (CMRO2) in five subjects. Hyperventilation-induced hypocapnia served as a control to verify the sensitivity of our measurements. During hypocapnia (~16 mmHg below resting values), Vp decreased by 40.0 ± 2.4% (95% CI, P < 0.001), while StO2 and tHb decreased by 2.9 ± 0.3% and 2.6 ± 0.4%, respectively (P = 0.003 and P = 0.002, respectively). CMRO2, calculated using the Fick equation, was reduced by 29.3 ± 9% compared to the isocapnic-euoxia baseline (P < 0.001). In the pharmacological experiments, there was a significant decrease in Vp, StO2, and tHb after ingestion of 200 mg of caffeine compared with placebo. There was no significant difference in CMRO2 between caffeine and placebo. Both showed a CMRO2 decline compared to baseline showing the importance of a placebo control. In conclusion, this study showed that profound hypocapnia impairs cerebral oxidative metabolism. We provide new insight into the effects of caffeine on cerebral hemodynamics. Moreover, this study showed that multimodal NIRS/TCD is an excellent tool for studying brain hemodynamic responses to pharmacological interventions and physiological challenges.
URI: http://hdl.handle.net/1880/51121
ISSN: 2051-817X
Appears in Collections:Dunn, Jeffrey F.

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