Abstract

Functional blood-oxygenation-level-dependent (BOLD) MRI provides a brain-wide readout that depends on the hemodynamic response to neuronal activity. Diffusion fMRI has been proposed as an alternative to BOLD fMRI and has been postulated to directly rely on neuronal activity. These complementary functional readouts are versatile tools to be combined with optogenetic stimulation to investigate networks of the brain. The cell-specificity and temporal precision of optogenetic manipulations promise to enable further investigation of the origin of fMRI signals. The signal characteristics of the diffusion fMRI readout vice versa may better resolve network effects of optogenetic stimulation. However, the light application needed for optogenetic stimulation is accompanied by heat deposition within the tissue. As both diffusion and BOLD are sensitive to temperature changes, light application can lead to apparent activations confounding the interpretation of fMRI data. The degree of tissue heating, the appearance of apparent activation in different fMRI sequences and the origin of these phenomena are not well understood. Here, we disentangled apparent activations in BOLD and diffusion measurements in rats from physiological activation upon sensory or optogenetic stimulation. Both, BOLD and diffusion fMRI revealed similar signal shapes upon sensory stimulation that differed clearly from those upon heating. Apparent activations induced by high-intensity light application were dominated by T2∗-effects and resulted in mainly negative signal changes. We estimated that even low-intensity light application used for optogenetic stimulation reduces the BOLD response close to the fiber by up to 0.4%. The diffusion fMRI signal contained T2, T2∗ and diffusion components. The apparent diffusion coefficient, which reflects the isolated diffusion component, showed negative changes upon both optogenetic and electric forepaw stimulation. In contrast, positive changes were detected upon high-intensity light application and thus ruled out heating as a major contributor to the diffusion fMRI signal.

Highlights

  • Functional MRI has become the most important neuroimaging modality, since it offers non-invasive, brainwide imaging of neuronal activity with high spatial and temporal resolution

  • In the first set of experiments safe limits for light intensities applied during optogenetic stimulation, which did not cause heating artifacts, were determined

  • In this study we investigated the functional MRI signal in GE-BOLD, SE-BOLD and diffusion Functional MRI (fMRI) measurements and characterized heating artifacts, which may be confounders in optogenetic fMRI studies

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Summary

Introduction

Functional MRI (fMRI) has become the most important neuroimaging modality, since it offers non-invasive, brainwide imaging of neuronal activity with high spatial and temporal resolution. One theory proposes that neuronal cells swell during activation, thereby hindering diffusion in the tissue, and, creating a signal change in diffusion-weighted fMRI sequences (Le Bihan, 2007; Tsurugizawa et al, 2013; Abe et al, 2017a). Controversies exist regarding the existence and the origin of diffusion fMRI signal changes (Miller et al, 2007; Jin and Kim, 2008; Autio et al, 2011; Bai et al, 2016). Despite this dissent about functional diffusion MRI, this readout appears suitable to investigate the neurophysiological response to optogenetic stimulation of neuronal circuitry of the brain

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