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Direct neuronal glucose uptake heralds activity-dependent increases in cerebral metabolism
Metabolically, the brain is a highly active organ that relies almost exclusively on glucose as its energy source. According to the astrocyte-to-neuron lactate shuttle hypothesis, glucose is taken up by astrocytes and converted to lactate, which is then oxidized by neurons. Here we show, using 2-phot...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410436/ https://www.ncbi.nlm.nih.gov/pubmed/25904018 http://dx.doi.org/10.1038/ncomms7807 |
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author | Lundgaard, Iben Li, Baoman Xie, Lulu Kang, Hongyi Sanggaard, Simon Haswell, John Douglas R Sun, Wei Goldman, Siri Blekot, Solomiya Nielsen, Michael Takano, Takahiro Deane, Rashid Nedergaard, Maiken |
author_facet | Lundgaard, Iben Li, Baoman Xie, Lulu Kang, Hongyi Sanggaard, Simon Haswell, John Douglas R Sun, Wei Goldman, Siri Blekot, Solomiya Nielsen, Michael Takano, Takahiro Deane, Rashid Nedergaard, Maiken |
author_sort | Lundgaard, Iben |
collection | PubMed |
description | Metabolically, the brain is a highly active organ that relies almost exclusively on glucose as its energy source. According to the astrocyte-to-neuron lactate shuttle hypothesis, glucose is taken up by astrocytes and converted to lactate, which is then oxidized by neurons. Here we show, using 2-photon imaging of a near-infrared 2-deoxyglucose analogue (2DG-IR), that glucose is taken up preferentially by neurons in awake behaving mice. Anesthesia suppressed neuronal 2DG-IR uptake and sensory stimulation was associated with a sharp increase in neuronal, but not astrocytic, 2DG-IR uptake. Moreover, hexokinase, which catalyze the first enzymatic steps in glycolysis, was highly enriched in neurons compared with astrocytes, in mouse as well as in human cortex. These observations suggest that brain activity and neuronal glucose metabolism are directly linked, and identifies the neuron as the principal locus of glucose uptake as visualized by functional brain imaging. |
format | Online Article Text |
id | pubmed-4410436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-44104362015-10-23 Direct neuronal glucose uptake heralds activity-dependent increases in cerebral metabolism Lundgaard, Iben Li, Baoman Xie, Lulu Kang, Hongyi Sanggaard, Simon Haswell, John Douglas R Sun, Wei Goldman, Siri Blekot, Solomiya Nielsen, Michael Takano, Takahiro Deane, Rashid Nedergaard, Maiken Nat Commun Article Metabolically, the brain is a highly active organ that relies almost exclusively on glucose as its energy source. According to the astrocyte-to-neuron lactate shuttle hypothesis, glucose is taken up by astrocytes and converted to lactate, which is then oxidized by neurons. Here we show, using 2-photon imaging of a near-infrared 2-deoxyglucose analogue (2DG-IR), that glucose is taken up preferentially by neurons in awake behaving mice. Anesthesia suppressed neuronal 2DG-IR uptake and sensory stimulation was associated with a sharp increase in neuronal, but not astrocytic, 2DG-IR uptake. Moreover, hexokinase, which catalyze the first enzymatic steps in glycolysis, was highly enriched in neurons compared with astrocytes, in mouse as well as in human cortex. These observations suggest that brain activity and neuronal glucose metabolism are directly linked, and identifies the neuron as the principal locus of glucose uptake as visualized by functional brain imaging. 2015-04-23 /pmc/articles/PMC4410436/ /pubmed/25904018 http://dx.doi.org/10.1038/ncomms7807 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Lundgaard, Iben Li, Baoman Xie, Lulu Kang, Hongyi Sanggaard, Simon Haswell, John Douglas R Sun, Wei Goldman, Siri Blekot, Solomiya Nielsen, Michael Takano, Takahiro Deane, Rashid Nedergaard, Maiken Direct neuronal glucose uptake heralds activity-dependent increases in cerebral metabolism |
title | Direct neuronal glucose uptake heralds activity-dependent increases in cerebral metabolism |
title_full | Direct neuronal glucose uptake heralds activity-dependent increases in cerebral metabolism |
title_fullStr | Direct neuronal glucose uptake heralds activity-dependent increases in cerebral metabolism |
title_full_unstemmed | Direct neuronal glucose uptake heralds activity-dependent increases in cerebral metabolism |
title_short | Direct neuronal glucose uptake heralds activity-dependent increases in cerebral metabolism |
title_sort | direct neuronal glucose uptake heralds activity-dependent increases in cerebral metabolism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410436/ https://www.ncbi.nlm.nih.gov/pubmed/25904018 http://dx.doi.org/10.1038/ncomms7807 |
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