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Brain sugar consumption during neuronal activation detected by CEST functional MRI at ultra-high magnetic fields. | LitMetric

Brain sugar consumption during neuronal activation detected by CEST functional MRI at ultra-high magnetic fields.

Sci Rep

NeuroSpin, Commissariat à l'Energie Atomique et aux Energies Alternatives, Univerisité Paris-Saclay, Gif-sur-Yvette, France.

Published: March 2019

AI Article Synopsis

Article Abstract

Blood oxygenation level dependent (BOLD) functional magnetic resonance imaging (fMRI) indirectly measures brain activity based on neurovascular coupling, a reporter that limits both the spatial and temporal resolution of the technique as well as the cellular and metabolic specificity. Emerging methods using functional spectroscopy (fMRS) and diffusion-weighted fMRI suggest that metabolic and structural modifications are also taking place in the activated cells. This paper explores an alternative metabolic imaging approach based on Chemical Exchange Saturation Transfer (CEST) to assess potential metabolic changes induced by neuronal stimulation in rat brains at 17.2 T. An optimized CEST-fMRI data acquisition and processing protocol was developed and used to experimentally assess the feasibility of glucoCEST-based fMRI. Images acquired under glucose-sensitizing conditions showed a substantial negative contrast that highlighted the same brain regions as those activated with BOLD-fMRI. We ascribe this novel fMRI contrast to CEST's ability to monitor changes in the local concentration of glucose, a metabolite closely coupled to neuronal activity. Our findings are in good agreement with literature employing other modalities. The use of CEST-based techniques for fMRI is not limited to glucose detection; other metabolic pathways involved in neuronal activation could be potentially probed. Moreover, being non invasive, it is conceivable that the same approach can be used for human studies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418181PMC
http://dx.doi.org/10.1038/s41598-019-40986-9DOI Listing

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