Author
Listed:
- Irmak Gezginer
(University of Zurich
ETH Zurich)
- Zhenyue Chen
(University of Zurich
ETH Zurich
Tongji University)
- Hikari A. I. Yoshihara
(University of Zurich
ETH Zurich)
- Xosé Luís Deán-Ben
(University of Zurich
ETH Zurich)
- Valerio Zerbi
(University of Geneva
University of Geneva)
- Daniel Razansky
(University of Zurich
ETH Zurich)
Abstract
Resting-state functional connectivity (rsFC) has been essential to elucidate the intricacy of brain organization, further revealing clinical biomarkers of neurological disorders. Although functional magnetic resonance imaging (fMRI) remains a cornerstone in the field of rsFC recordings, its interpretation is often hindered by the convoluted physiological origin of the blood-oxygen-level-dependent (BOLD) contrast affected by multiple factors. Here, we capitalize on the unique concurrent multiparametric hemodynamic recordings of a hybrid magnetic resonance optoacoustic tomography platform to comprehensively characterize rsFC in female mice. The unique blood oxygenation readings and high spatio-temporal resolution at depths provided by functional optoacoustic (fOA) imaging offer an effective means for elucidating the connection between BOLD and hemoglobin responses. Seed-based and independent component analyses reveal spatially overlapping bilateral correlations between the fMRI-BOLD readings and the multiple hemodynamic components measured with fOA but also subtle discrepancies, particularly in anti-correlations. Notably, total hemoglobin and oxygenated hemoglobin components are found to exhibit stronger correlation with BOLD than deoxygenated hemoglobin, challenging conventional assumptions on the BOLD signal origin.
Suggested Citation
Irmak Gezginer & Zhenyue Chen & Hikari A. I. Yoshihara & Xosé Luís Deán-Ben & Valerio Zerbi & Daniel Razansky, 2024.
"Concurrent optoacoustic tomography and magnetic resonance imaging of resting-state functional connectivity in the mouse brain,"
Nature Communications, Nature, vol. 15(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-54947-y
DOI: 10.1038/s41467-024-54947-y
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