TY - JOUR
T1 - More than just summed neuronal activity
T2 - How multiple cell types shape the BOLD response: Cellular mechanisms underlying BOLD
AU - Howarth, Clare
AU - Mishra, Anusha
AU - Hall, Catherine N.
N1 - Funding Information:
(grant no. 1R01NS110690), NIH NIMH (grant no. 1R01DA047237) and NIH NIA (grant no. P30AG066518-01; Oregon Alzheimer’s Disease Research Center, PI: Kaye). C.N.H. is funded by the Medical
Funding Information:
Data accessibility. This article has no additional data. Authors’ contributions. All authors contributed equally to this manuscript. Competing interests. We declare we have no competing interests. Funding. C.H. is funded by a Sir Henry Dale Fellowship jointly funded by the Wellcome Trust and the Royal Society (grant no. 105586/Z/ 14/Z). A.M. is funded by Collins Medical Trust, NIH NINDS
Publisher Copyright:
© 2020 The Author(s).
PY - 2021/1/4
Y1 - 2021/1/4
N2 - Functional neuroimaging techniques are widely applied to investigations of human cognition and disease. The most commonly used among these is blood oxygen level-dependent (BOLD) functional magnetic resonance imaging. The BOLD signal occurs because neural activity induces an increase in local blood supply to support the increased metabolism that occurs during activity. This supply usually outmatches demand, resulting in an increase in oxygenated blood in an active brain region, and a corresponding decrease in deoxygenated blood, which generates the BOLD signal. Hence, the BOLD response is shaped by an integration of local oxygen use, through metabolism, and supply, in the blood. To understand what information is carried in BOLD signals, we must understand how several cell types in the brain-local excitatory neurons, inhibitory neurons, astrocytes and vascular cells (pericytes, vascular smooth muscle and endothelial cells), and their modulation by ascending projection neurons-contribute to both metabolism and haemodynamic changes. Here, we review the contributions of each cell type to the regulation of cerebral blood flow and metabolism, and discuss situations where a simplified interpretation of the BOLD response as reporting local excitatory activity may misrepresent important biological phenomena, for example with regards to arousal states, ageing and neurological disease. This article is part of the theme issue 'Key relationships between non-invasive functional neuroimaging and the underlying neuronal activity'.
AB - Functional neuroimaging techniques are widely applied to investigations of human cognition and disease. The most commonly used among these is blood oxygen level-dependent (BOLD) functional magnetic resonance imaging. The BOLD signal occurs because neural activity induces an increase in local blood supply to support the increased metabolism that occurs during activity. This supply usually outmatches demand, resulting in an increase in oxygenated blood in an active brain region, and a corresponding decrease in deoxygenated blood, which generates the BOLD signal. Hence, the BOLD response is shaped by an integration of local oxygen use, through metabolism, and supply, in the blood. To understand what information is carried in BOLD signals, we must understand how several cell types in the brain-local excitatory neurons, inhibitory neurons, astrocytes and vascular cells (pericytes, vascular smooth muscle and endothelial cells), and their modulation by ascending projection neurons-contribute to both metabolism and haemodynamic changes. Here, we review the contributions of each cell type to the regulation of cerebral blood flow and metabolism, and discuss situations where a simplified interpretation of the BOLD response as reporting local excitatory activity may misrepresent important biological phenomena, for example with regards to arousal states, ageing and neurological disease. This article is part of the theme issue 'Key relationships between non-invasive functional neuroimaging and the underlying neuronal activity'.
KW - BOLD fMRI
KW - astrocyte
KW - endothelial propagation
KW - interneuron
KW - neurometabolic coupling
KW - neurovascular coupling
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U2 - 10.1098/rstb.2019.0630
DO - 10.1098/rstb.2019.0630
M3 - Review article
C2 - 33190598
AN - SCOPUS:85096269778
SN - 0962-8436
VL - 376
JO - Philosophical Transactions of the Royal Society B: Biological Sciences
JF - Philosophical Transactions of the Royal Society B: Biological Sciences
IS - 1815
M1 - 20190630
ER -