Perception is associated with the brain’s metabolic response to sensory stimulation

Author:

DiNuzzo Mauro1ORCID,Mangia Silvia2ORCID,Moraschi Marta3ORCID,Mascali Daniele14ORCID,Hagberg Gisela E5ORCID,Giove Federico16ORCID

Affiliation:

1. Museo Storico della Fisica e Centro Studi e Ricerche Enrico Fermi

2. Center for Magnetic Resonance Research, Department of Radiology, University of Minnesota

3. Department of Radiation Oncology, Campus Bio-Medico University of Rome

4. Dipartimento di Neuroscienze, Imaging e Scienze Cliniche, Università Gabriele D’Annunzio

5. Biomedical Magnetic Resonance, University Hospital Tübingen and High–Field Magnetic Resonance, Max Planck Institute for Biological Cybernetics

6. Fondazione Santa Lucia IRCCS

Abstract

Processing of incoming sensory stimulation triggers an increase of cerebral perfusion and blood oxygenation (neurovascular response) as well as an alteration of the metabolic neurochemical profile (neurometabolic response). Here, we show in human primary visual cortex (V1) that perceived and unperceived isoluminant chromatic flickering stimuli designed to have similar neurovascular responses as measured by blood oxygenation level-dependent functional magnetic resonance imaging (BOLD-fMRI) have markedly different neurometabolic responses as measured by proton functional magnetic resonance spectroscopy (1H-fMRS). In particular, a significant regional buildup of lactate, an index of aerobic glycolysis, and glutamate, an index of malate–aspartate shuttle, occurred in V1 only when the flickering was perceived, without any relation with other behavioral or physiological variables. Whereas the BOLD-fMRI signal in V1, a proxy for input to V1, was insensitive to flickering perception by design, the BOLD-fMRI signal in secondary visual areas was larger during perceived than unperceived flickering, indicating increased output from V1. These results demonstrate that the upregulation of energy metabolism induced by visual stimulation depends on the type of information processing taking place in V1, and that 1H-fMRS provides unique information about local input/output balance that is not measured by BOLD-fMRI.

Funder

Ministero della Salute

Max Planck Institute for Biological Cybernetics

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference119 articles.

1. Cerebral Metabolic Changes During Sleep;Aalling;Current Neurology and Neuroscience Reports,2018

2. No attentional capture from invisible flicker;Alais;Scientific Reports,2016

3. Nicotine excites VIP interneurons to disinhibit pyramidal neurons in auditory cortex;Askew;Synapse (New York, N.Y.),2019

4. Neurochemical and BOLD responses during neuronal activation measured in the human visual cortex at 7 Tesla;Bednařík;Journal of Cerebral Blood Flow and Metabolism,2015

5. Neurochemical responses to chromatic and achromatic stimuli in the human visual cortex;Bednařík;Journal of Cerebral Blood Flow and Metabolism,2018

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