Evidence that the negative BOLD response is neuronal in origin: a simultaneous EEG–BOLD–CBF study in humans

Unambiguous interpretation of changes in the BOLD signal is challenging because of the complex neurovascular coupling that translates changes in neuronal activity into the subsequent haemodynamic response. In particular, the neurophysiological origin of the negative BOLD response (NBR) remains incom...

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Main Authors: Mullinger, Karen J., Mayhew, Stephen D., Bagshaw, Andrew P., Bowtell, Richard W., Francis, Susan T.
Format: Article
Published: Elsevier 2014
Online Access:https://eprints.nottingham.ac.uk/35148/
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author Mullinger, Karen J.
Mayhew, Stephen D.
Bagshaw, Andrew P.
Bowtell, Richard W.
Francis, Susan T.
author_facet Mullinger, Karen J.
Mayhew, Stephen D.
Bagshaw, Andrew P.
Bowtell, Richard W.
Francis, Susan T.
author_sort Mullinger, Karen J.
building Nottingham Research Data Repository
collection Online Access
description Unambiguous interpretation of changes in the BOLD signal is challenging because of the complex neurovascular coupling that translates changes in neuronal activity into the subsequent haemodynamic response. In particular, the neurophysiological origin of the negative BOLD response (NBR) remains incompletely understood. Here, we simultaneously recorded BOLD, EEG and cerebral blood flow (CBF) responses to 10 s blocks of unilateral median nerve stimulation (MNS) in order to interrogate the NBR. Both negative BOLD and negative CBF responses to MNS were observed in the same region of the ipsilateral primary sensorimotor cortex (S1/M1) and calculations showed that MNS induced a decrease in the cerebral metabolic rate of oxygen consumption (CMRO2) in this NBR region. The ∆CMRO2/∆CBF coupling ratio (n) was found to be significantly larger in this ipsilateral S1/M1 region (n = 0.91 ± 0.04, M = 10.45%) than in the contralateral S1/M1 (n = 0.65 ± 0.03, M = 10.45%) region that exhibited a positive BOLD response (PBR) and positive CBF response, and a consequent increase in CMRO2 during MNS. The fMRI response amplitude in ipsilateral S1/M1 was negatively correlated with both the power of the 8–13 Hz EEG mu oscillation and somatosensory evoked potential amplitude. Blocks in which the largest magnitude of negative BOLD and CBF responses occurred therefore showed greatest mu power, an electrophysiological index of cortical inhibition, and largest somatosensory evoked potentials. Taken together, our results suggest that a neuronal mechanism underlies the NBR, but that the NBR may originate from a different neurovascular coupling mechanism to the PBR, suggesting that caution should be taken in assuming the NBR simply represents the neurophysiological inverse of the PBR.
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spelling nottingham-351482020-05-04T16:48:45Z https://eprints.nottingham.ac.uk/35148/ Evidence that the negative BOLD response is neuronal in origin: a simultaneous EEG–BOLD–CBF study in humans Mullinger, Karen J. Mayhew, Stephen D. Bagshaw, Andrew P. Bowtell, Richard W. Francis, Susan T. Unambiguous interpretation of changes in the BOLD signal is challenging because of the complex neurovascular coupling that translates changes in neuronal activity into the subsequent haemodynamic response. In particular, the neurophysiological origin of the negative BOLD response (NBR) remains incompletely understood. Here, we simultaneously recorded BOLD, EEG and cerebral blood flow (CBF) responses to 10 s blocks of unilateral median nerve stimulation (MNS) in order to interrogate the NBR. Both negative BOLD and negative CBF responses to MNS were observed in the same region of the ipsilateral primary sensorimotor cortex (S1/M1) and calculations showed that MNS induced a decrease in the cerebral metabolic rate of oxygen consumption (CMRO2) in this NBR region. The ∆CMRO2/∆CBF coupling ratio (n) was found to be significantly larger in this ipsilateral S1/M1 region (n = 0.91 ± 0.04, M = 10.45%) than in the contralateral S1/M1 (n = 0.65 ± 0.03, M = 10.45%) region that exhibited a positive BOLD response (PBR) and positive CBF response, and a consequent increase in CMRO2 during MNS. The fMRI response amplitude in ipsilateral S1/M1 was negatively correlated with both the power of the 8–13 Hz EEG mu oscillation and somatosensory evoked potential amplitude. Blocks in which the largest magnitude of negative BOLD and CBF responses occurred therefore showed greatest mu power, an electrophysiological index of cortical inhibition, and largest somatosensory evoked potentials. Taken together, our results suggest that a neuronal mechanism underlies the NBR, but that the NBR may originate from a different neurovascular coupling mechanism to the PBR, suggesting that caution should be taken in assuming the NBR simply represents the neurophysiological inverse of the PBR. Elsevier 2014-07-01 Article PeerReviewed Mullinger, Karen J., Mayhew, Stephen D., Bagshaw, Andrew P., Bowtell, Richard W. and Francis, Susan T. (2014) Evidence that the negative BOLD response is neuronal in origin: a simultaneous EEG–BOLD–CBF study in humans. NeuroImage, 94 . pp. 263-274. ISSN 1095-9572 http://www.sciencedirect.com/science/article/pii/S1053811914001426 doi:10.1016/j.neuroimage.2014.02.029 doi:10.1016/j.neuroimage.2014.02.029
spellingShingle Mullinger, Karen J.
Mayhew, Stephen D.
Bagshaw, Andrew P.
Bowtell, Richard W.
Francis, Susan T.
Evidence that the negative BOLD response is neuronal in origin: a simultaneous EEG–BOLD–CBF study in humans
title Evidence that the negative BOLD response is neuronal in origin: a simultaneous EEG–BOLD–CBF study in humans
title_full Evidence that the negative BOLD response is neuronal in origin: a simultaneous EEG–BOLD–CBF study in humans
title_fullStr Evidence that the negative BOLD response is neuronal in origin: a simultaneous EEG–BOLD–CBF study in humans
title_full_unstemmed Evidence that the negative BOLD response is neuronal in origin: a simultaneous EEG–BOLD–CBF study in humans
title_short Evidence that the negative BOLD response is neuronal in origin: a simultaneous EEG–BOLD–CBF study in humans
title_sort evidence that the negative bold response is neuronal in origin: a simultaneous eeg–bold–cbf study in humans
url https://eprints.nottingham.ac.uk/35148/
https://eprints.nottingham.ac.uk/35148/
https://eprints.nottingham.ac.uk/35148/