Multi-Modal Imaging: From Animal Models to Human
Catie Chang1

1Vanderbilt University, United States

Synopsis

Integrating fMRI with complementary neurophysiological measurements can provide a more comprehensive understanding of brain function, and help to clarify the neural basis of BOLD fMRI signals. Here, we will discuss multi-modal imaging studies of the human brain using simultaneous EEG-fMRI, along with studies in animal models, which allow for more direct, invasive monitoring and manipulation of neural circuits. This talk will also briefly discuss technical challenges and methodology involved in acquiring and analyzing simultaneous fMRI-electrophysiological data.

Target Audience

Researchers interested in multi-modal brain imaging (such as simultaneous EEG-fMRI) and the neural basis of the BOLD fMRI signal.

Educational Objectives

- Identify key benefits and challenges involved in combining fMRI with complementary measurements of neural activity

- Identify ways in which multi-modal imaging can help to elucidate the neural basis of BOLD fMRI signals

Overview

Functional MRI (fMRI) is a widely used, non-invasive technology for investigating human brain function, as it allows for whole-brain coverage and spatial resolution of millimeters and below. Yet, the blood-oxygen level dependent (BOLD) fMRI response is an indirect, hemodynamic indicator of brain activity, and inferences drawn from fMRI are limited by our incomplete understanding of the neural and physiological processes that influence fMRI signals. On the other hand, techniques that provide more direct measures of neural activity (such as EEG and invasive electrophysiology) can offer millisecond-scale temporal resolution, but are limited by either coarse spatial resolution or restricted spatial coverage. Here, we will discuss how integrating fMRI and electrophysiological signals can leverage the complementary strengths of these modalities, as well as help to clarify the neural basis of fMRI signals.

In humans, multi-modal imaging can be carried out noninvasively by recording scalp EEG concurrently with fMRI [1]. EEG and fMRI can be combined to examine cognitive processes [2] as well as spontaneous brain activity and resting-state networks [3-5]. As EEG provides established markers of brain state, simultaneous EEG-fMRI has been applied for studying state-dependent human brain activity and network connectivity; for example, across vigilance levels [6,7] and during sleep (e.g., reviewed in [8]).

In animal models, invasive recordings and manipulations of neural activity can more readily be performed. Measures such as single- and multi-unit activity, local field potentials, and astrocytic calcium signals can be recorded together with whole-brain fMRI to investigate neural circuits and to examine the neurophysiological basis of fMRI [9-12]. Further, targeted manipulation of neural activity can be combined with fMRI to examine brain-wide effects of specific perturbations (e.g. [13-15]).

Acknowledgements

No acknowledgement found.

References

[1] Ritter P, Villringer A. Simultaneous EEG-fMRI. Neurosci Biobehav Rev. 2006;30(6):823-38

[2] Debener et al. Single-trial EEG-fMRI reveals the dynamics of cognitive function. Trends Cogn Sci. 2006 Dec;10(12):558-63.

[3] Goldman RI, Stern JM, Engel J Jr, Cohen MS. Simultaneous EEG and fMRI of the alpha rhythm. Neuroreport. 2002 Dec 20;13(18):2487-92.

[4] Mantini D, Perrucci MG, Del Gratta C, Romani GL, Corbetta M. Electrophysiological signatures of resting state networks in the human brain. Proc Natl Acad Sci U S A. 2007 Aug 7;104(32):13170-5.

[5] Tagliazucchi E, Laufs H. Multimodal imaging of dynamic functional connectivity. Front Neurol. 2015 Feb 16;6:10.

[6] Wong CW, Olafsson V, Tal O, Liu TT. The amplitude of the resting-state fMRI global signal is related to EEG vigilance measures. Neuroimage. 2013 Dec;83:983-90.

[7] Chang C, Liu Z, Chen MC, Liu X, Duyn JH. EEG correlates of time-varying BOLD functional connectivity. Neuroimage. 2013 May 15;72:227-36.

[8] Duyn JH. EEG-fMRI Methods for the Study of Brain Networks during Sleep. Front Neurol. 2012 Jul 2;3:100.

[9] Logothetis NK, Pauls J, Augath M, Trinath T, Oeltermann A. Neurophysiological investigation of the basis of the fMRI signal. Nature. 2001 Jul 12;412(6843):150-7.

[10] Wang M, He Y, Sejnowski T, Yu X. Brain-state dependent astrocytic Ca2+ signals are coupled to both positive and negative BOLD-fMRI signals. Proc Natl Acad Sci U S A. 2018 Feb 13;115(7):E1647-E1656.

[11] Park SH et al. Functional Subpopulations of Neurons in a Macaque Face Patch Revealed by Single-Unit fMRI Mapping. Neuron. 2017 Aug 16;95(4):971-981.

[12] Thompson GJ, Pan WJ, Magnuson ME, Jaeger D, Keilholz SD. Quasi-periodic patterns (QPP): large-scale dynamics in resting state fMRI that correlate with local infraslow electrical activity. Neuroimage. 2014 Jan 1;84:1018-31.

[13] Lee JH, Kreitzer AC, Singer AC, Schiff ND. Illuminating Neural Circuits: From Molecules to MRI. J Neurosci. 2017 Nov 8;37(45):10817-10825.

[14] Turchi J, Chang C, Ye FQ, Russ BE, Yu DK, Cortes CR, Monosov IE, Duyn JH, Leopold DA. The Basal Forebrain Regulates Global Resting-State fMRI Fluctuations. Neuron. 2018 Feb 21;97(4):940-952.e4

[15] Grayson DS, Bliss-Moreau E, Machado CJ, Bennett J, Shen K, Grant KA, Fair DA, Amaral DG. The Rhesus Monkey Connectome Predicts Disrupted Functional Networks Resulting from Pharmacogenetic Inactivation of the Amygdala. Neuron. 2016 Jul 20;91(2):453-66.

Proc. Intl. Soc. Mag. Reson. Med. 27 (2019)