TY - JOUR
T1 - Physiological origin for the BOLD poststimulus undershoot in human brain
T2 - Vascular compliance versus oxygen metabolism
AU - Hua, Jun
AU - Stevens, Robert D.
AU - Huang, Alan J.
AU - Pekar, James J.
AU - Van Zijl, Peter C.M.
PY - 2011/7
Y1 - 2011/7
N2 - The poststimulus blood oxygenation level-dependent (BOLD) undershoot has been attributed to two main plausible origins: delayed vascular compliance based on delayed cerebral blood volume (CBV) recovery and a sustained increased oxygen metabolism after stimulus cessation. To investigate these contributions, multimodal functional magnetic resonance imaging was employed to monitor responses of BOLD, cerebral blood flow (CBF), total CBV, and arterial CBV (CBVa) in human visual cortex after brief breath hold and visual stimulation. In visual experiments, after stimulus cessation, CBVa was restored to baseline in 7.9±3.4 seconds, and CBF and CBV in 14.8±5.0 seconds and 16.1±5.8 seconds, respectively, all significantly faster than BOLD signal recovery after undershoot (28.1±5.5 seconds). During the BOLD undershoot, postarterial CBV (CBV pa, capillaries and venules) was slightly elevated (2.41.8%), and cerebral metabolic rate of oxygen (CMRO2) was above baseline (10.6±7.4%). Following breath hold, however, CBF, CBV, CBV a and BOLD signals all returned to baseline in 20 seconds. No significant BOLD undershoot, and residual CBV pa dilation were observed, and CMRO2 did not substantially differ from baseline. These data suggest that both delayed CBV pa recovery and enduring increased oxidative metabolism impact the BOLD undershoot. Using a biophysical model, their relative contributions were estimated to be 19.7±15.9% and 78.7±18.6%, respectively.
AB - The poststimulus blood oxygenation level-dependent (BOLD) undershoot has been attributed to two main plausible origins: delayed vascular compliance based on delayed cerebral blood volume (CBV) recovery and a sustained increased oxygen metabolism after stimulus cessation. To investigate these contributions, multimodal functional magnetic resonance imaging was employed to monitor responses of BOLD, cerebral blood flow (CBF), total CBV, and arterial CBV (CBVa) in human visual cortex after brief breath hold and visual stimulation. In visual experiments, after stimulus cessation, CBVa was restored to baseline in 7.9±3.4 seconds, and CBF and CBV in 14.8±5.0 seconds and 16.1±5.8 seconds, respectively, all significantly faster than BOLD signal recovery after undershoot (28.1±5.5 seconds). During the BOLD undershoot, postarterial CBV (CBV pa, capillaries and venules) was slightly elevated (2.41.8%), and cerebral metabolic rate of oxygen (CMRO2) was above baseline (10.6±7.4%). Following breath hold, however, CBF, CBV, CBV a and BOLD signals all returned to baseline in 20 seconds. No significant BOLD undershoot, and residual CBV pa dilation were observed, and CMRO2 did not substantially differ from baseline. These data suggest that both delayed CBV pa recovery and enduring increased oxidative metabolism impact the BOLD undershoot. Using a biophysical model, their relative contributions were estimated to be 19.7±15.9% and 78.7±18.6%, respectively.
KW - BOLD undershoot
KW - MRI
KW - cerebral blood flow
KW - cerebral blood volume
KW - hypercapnia
KW - oxygen metabolism
UR - http://www.scopus.com/inward/record.url?scp=79959847484&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79959847484&partnerID=8YFLogxK
U2 - 10.1038/jcbfm.2011.35
DO - 10.1038/jcbfm.2011.35
M3 - Article
C2 - 21468090
AN - SCOPUS:79959847484
SN - 0271-678X
VL - 31
SP - 1599
EP - 1611
JO - Journal of Cerebral Blood Flow and Metabolism
JF - Journal of Cerebral Blood Flow and Metabolism
IS - 7
ER -