TY - JOUR
T1 - Arterial CO2 fluctuations modulate neuronal rhythmicity
T2 - Implications for MEG and FMRI studies of resting-state networks
AU - Driver, Ian D.
AU - Whittaker, Joseph R.
AU - Bright, Molly G.
AU - Muthukumaraswamy, Suresh D.
AU - Murphy, Kevin
N1 - Funding Information:
This work was supported by the Wellcome Trust (Grant WT090199). We thank Gavin Perry with assistance with data acquisition and Krish Singh for constructive comments on this work.
Publisher Copyright:
© 2016 the authors.
PY - 2016/8/17
Y1 - 2016/8/17
N2 - A fast emerging technique for studying human resting state networks (RSNs) is based on spontaneous temporal fluctuations in neuronal oscillatory power, as measured by magnetoencephalography. However, it has been demonstrated recently that this power is sensitive to modulations in arterial CO2 concentration. Arterial CO2 can be modulated by natural fluctuations in breathing pattern, as might typically occur during the acquisition of an RSN experiment. Here, we demonstrate for the first time the fine-scale dependence of neuronal oscillatory power on arterial CO2 concentration, showing that reductions in alpha, beta, and gamma power are observed with even very mild levels of hypercapnia (increased arterialCO2). We use a graded hypercapnia paradigm and participant feedback to rule out a sensory cause, suggesting a predominantly physiological origin. Furthermore, we demonstrate that natural fluctuations in arterial CO2, without administration of inspired CO2, are of a sufficient level to influence neuronal oscillatory power significantly in the delta-, alpha-, beta-, and gamma-frequency bands. A more thorough understanding of the relationship between physiological factors and cortical rhythmicity is required. In light of these findings, existing results, paradigms, and analysis techniques for the study of resting-state brain data should be revisited.
AB - A fast emerging technique for studying human resting state networks (RSNs) is based on spontaneous temporal fluctuations in neuronal oscillatory power, as measured by magnetoencephalography. However, it has been demonstrated recently that this power is sensitive to modulations in arterial CO2 concentration. Arterial CO2 can be modulated by natural fluctuations in breathing pattern, as might typically occur during the acquisition of an RSN experiment. Here, we demonstrate for the first time the fine-scale dependence of neuronal oscillatory power on arterial CO2 concentration, showing that reductions in alpha, beta, and gamma power are observed with even very mild levels of hypercapnia (increased arterialCO2). We use a graded hypercapnia paradigm and participant feedback to rule out a sensory cause, suggesting a predominantly physiological origin. Furthermore, we demonstrate that natural fluctuations in arterial CO2, without administration of inspired CO2, are of a sufficient level to influence neuronal oscillatory power significantly in the delta-, alpha-, beta-, and gamma-frequency bands. A more thorough understanding of the relationship between physiological factors and cortical rhythmicity is required. In light of these findings, existing results, paradigms, and analysis techniques for the study of resting-state brain data should be revisited.
KW - Cortical oscillations
KW - Functional connectivity
KW - Hypercapnia
KW - Magnetoencephalography
KW - Physiological noise
UR - http://www.scopus.com/inward/record.url?scp=84982284779&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84982284779&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.4263-15.2016
DO - 10.1523/JNEUROSCI.4263-15.2016
M3 - Article
C2 - 27535903
AN - SCOPUS:84982284779
SN - 0270-6474
VL - 36
SP - 8541
EP - 8550
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 33
ER -