Modification of oxygen consumption and blood flow in mouse somatosensory cortex by cell-type-specific neuronal activity
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Modification of oxygen consumption and blood flow in mouse somatosensory cortex by cell-type-specific neuronal activity. / Dahlqvist, Matilda K; Thomsen, Kirsten J; Postnov, Dmitry D; Lauritzen, Martin J.
In: Journal of Cerebral Blood Flow and Metabolism, Vol. 40, No. 10, 2020, p. 2010-2025.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Modification of oxygen consumption and blood flow in mouse somatosensory cortex by cell-type-specific neuronal activity
AU - Dahlqvist, Matilda K
AU - Thomsen, Kirsten J
AU - Postnov, Dmitry D
AU - Lauritzen, Martin J
PY - 2020
Y1 - 2020
N2 - Gamma activity arising from the interplay between pyramidal neurons and fast-spiking parvalbumin (PV) interneurons is an integral part of higher cognitive functions and is assumed to contribute significantly to brain metabolic responses. Cerebral metabolic rate of oxygen (CMRO2) responses were evoked by optogenetic stimulation of cortical PV interneurons and pyramidal neurons. We found that CMRO2 responses depended on neuronal activation, but not on the power of gamma activity induced by optogenetic stimulation. This implies that evoked gamma activity per se is not energy demanding. Optogenetic stimulation of PV interneurons during somatosensory stimulation reduced excitatory neuronal activity but did not potentiate O-2 consumption as previously hypothesized. In conclusion, our data suggest that activity-driven CMRO2 responses depend on neuronal excitation rather than the cerebral rhythmic activity they induce. Excitation of both excitatory and inhibitory neurons requires energy, but inhibition of cortical excitatory neurons by interneurons does not potentiate activity-driven energy consumption.
AB - Gamma activity arising from the interplay between pyramidal neurons and fast-spiking parvalbumin (PV) interneurons is an integral part of higher cognitive functions and is assumed to contribute significantly to brain metabolic responses. Cerebral metabolic rate of oxygen (CMRO2) responses were evoked by optogenetic stimulation of cortical PV interneurons and pyramidal neurons. We found that CMRO2 responses depended on neuronal activation, but not on the power of gamma activity induced by optogenetic stimulation. This implies that evoked gamma activity per se is not energy demanding. Optogenetic stimulation of PV interneurons during somatosensory stimulation reduced excitatory neuronal activity but did not potentiate O-2 consumption as previously hypothesized. In conclusion, our data suggest that activity-driven CMRO2 responses depend on neuronal excitation rather than the cerebral rhythmic activity they induce. Excitation of both excitatory and inhibitory neurons requires energy, but inhibition of cortical excitatory neurons by interneurons does not potentiate activity-driven energy consumption.
U2 - 10.1177/0271678X19882787
DO - 10.1177/0271678X19882787
M3 - Journal article
C2 - 31645177
VL - 40
SP - 2010
EP - 2025
JO - Journal of Cerebral Blood Flow and Metabolism
JF - Journal of Cerebral Blood Flow and Metabolism
SN - 0271-678X
IS - 10
ER -
ID: 229311682