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Investigating the post-stimulus undershoot of the BOLD signal: A simultaneous fMRI and fNIRS study

MPG-Autoren
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Schroeter,  Matthias L.
Department Cognitive Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Kupka,  Thomas
Department Cognitive Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Mildner,  Toralf
Methods and Development Unit Nuclear Magnetic Resonance, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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von Cramon,  D. Yves
Department Cognitive Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Schroeter, M. L., Kupka, T., Mildner, T., Uludag, K., & von Cramon, D. Y. (2006). Investigating the post-stimulus undershoot of the BOLD signal: A simultaneous fMRI and fNIRS study. NeuroImage, 30(2), 349-358. doi:10.1016/j.neuroimage.2005.09.048.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-0010-BF8F-9
Zusammenfassung
Measuring the hemodynamic response with functional magnetic resonance imaging (fMRI) together with functional near-infrared spectroscopy (fNIRS) may overcome limitations of single-method approaches. Accordingly, we measured the event-related hemodynamic response with both imaging methods simultaneously in young subjects during visual stimulation. An intertrial interval of 60 s was chosen to include the prolonged post-stimulus undershoot of the blood oxygenation level dependent (BOLD) signal. During visual stimulation, the BOLD signal, oxy-, and total hemoglobin (Hb) increased, whereas deoxy-Hb decreased. The post-stimulus period was characterized by an undershoot of the BOLD signal, oxy-Hb, and an overshoot of deoxy-Hb. Total Hb as measured by fNIRS returned to baseline immediately after the end of stimulation. Results suggest that the post-stimulus events as measured by fNIRS are dominated by a prolonged high-level oxygen consumption in the microvasculature. The contribution of a delayed return of blood volume to the BOLD post-stimulus undershoot in post-capillary veins as suggested by the Balloon and Windkessel models remains ambiguous. Temporal changes in the BOLD signal were highly correlated with deoxy-Hb, with lower correlation values for oxy- and total Hb. Furthermore, data show that fNIRS covers the outer 1 cm of the brain cortex. These results were confirmed by simultaneous fMRI/fNIRS measurements during rest. In conclusion, multimodal imaging approaches may contribute to the understanding of neurovascular coupling.