| Literature DB >> 29845643 |
Norio Takata1,2, Yuki Sugiura3, Keitaro Yoshida1, Miwako Koizumi1, Nishida Hiroshi1, Kurara Honda3, Ryutaro Yano4, Yuji Komaki2, Ko Matsui5, Makoto Suematsu3, Masaru Mimura1, Hideyuki Okano4,6, Kenji F Tanaka1.
Abstract
Functional magnetic resonance imaging (fMRI) based on the blood oxygenation level-dependent (BOLD) signal has been used to infer sites of neuronal activation in the brain. A recent study demonstrated, however, unexpected BOLD signal generation without neuronal excitation, which led us to hypothesize the presence of another cellular source for BOLD signal generation. Collective assessment of optogenetic activation of astrocytes or neurons, fMRI in awake mice, electrophysiological measurements, and histochemical detection of neuronal activation, coherently suggested astrocytes as another cellular source. Unexpectedly, astrocyte-evoked BOLD signal accompanied oxygen consumption without modulation of neuronal activity. Imaging mass spectrometry of brain sections identified synthesis of acetyl-carnitine via oxidative glucose metabolism at the site of astrocyte-, but not neuron-evoked BOLD signal. Our data provide causal evidence that astrocytic activation alone is able to evoke BOLD signal response, which may lead to reconsideration of current interpretation of BOLD signal as a marker of neuronal activation.Entities:
Keywords: BOLD; astrocytes; fMRI; imaging mass spectrometry; optogenetics
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Year: 2018 PMID: 29845643 DOI: 10.1002/glia.23454
Source DB: PubMed Journal: Glia ISSN: 0894-1491 Impact factor: 7.452