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Astrocyte glutamate uptake impacts [ 18 F]FDG‐PET signal
Author(s) -
da Rocha Andreia Silva,
de Souza Débora Guerini,
Bellaver Bruna,
Fontana Igor C.,
Machado Luiza Santos,
Venturin Gianina Teribele,
Greggio Samuel,
da Costa Jaderson Costa,
Souza Diogo O.,
Zimmer Eduardo R.
Publication year - 2020
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1002/alz.044918
Subject(s) - glutamate receptor , astrocyte , striatum , hippocampus , neuroscience , glucose uptake , endocrinology , positron emission tomography , medicine , pharmacology , biology , central nervous system , dopamine , receptor , insulin
Background The role of astrocytes on brain functioning has become an important topic of debate. In this regard, an issue that still remains controversial is the astrocytes contribution to glucose brain metabolism and, therefore, to the uptake of 2‐Deoxy‐2‐[ 18 F]Fluoroglucose([ 18 F]FDG) detected by positron emission tomography(PET). For many years, it was widely assumed that the brain [ 18 F]FDG‐PET signal directly reflects the neuronal use of glucose, overlooking the possible participation of other brain cells. Recently, rodent and human studies have demonstrated that astrocytes may contribute to [ 18 F]FDG‐PET signal. To further explore these early findings, here, we used a pharmacological challenge on rodents. Clozapine was selected because it is known to decrease, on astrocytes, glutamate transport and the glutamate transporter 1 (GLT‐1) levels, an important trigger for glucose uptake in astrocytes. Methods Clozapine was administered for six weeks (25‐35mg/kg) to adult Wistar rats. Glucose brain metabolism was assessed using [ 18 F]FDG‐microPET before and after the treatment. [ 3 H]D‐Aspartate uptake was evaluated on brain slices. [ 3 H]Glutamate release was analyzed on synaptosomal preparations. [ 3 H]D‐Aspartate and [ 3 H]2‐Deoxyglucose uptake were analyzed on primary cortical astrocytic and neuronal cultures treated with clozapine (50uM) for 48h. Immunocontent and expression of GLT‐1 and Glutamate‐Aspartate Transporter(GLAST) were assessed on the cortical tissue and cell cultures. Results Clozapine treatment significantly reduced [ 18 F]FDG metabolism in the cerebral cortex, hippocampus, and striatum of adult rats. In addition, clozapine decreased cortical glutamate transport in brain slices – indexed by [ 3 H]D‐Aspartate uptake – and reduced the cortical immunocontent and expression of GLT‐1. Astrocytic cultures treated with clozapine presented a decline on GLT‐1 density, [ 3 H]D‐Aspartate uptake and [ 3 H]2‐Deoxyglucose uptake, while the neuronal cultures presented no changes. Conclusion Here, we present microPET data showing that a challenge with clozapine causes a reduction on [ 18 F]FDG signal in brain regions presenting high GLT‐1 density. Our cell culture findings indicate that astrocytes are, at least partially, the cells underlying the brain glucose metabolism response to clozapine. These results corroborate previous studies that highlight the need for a reevaluation in the way that brain [ 18 F]FDG‐PET data is interpreted. Additionally, clozapine is a drug approved for clinical use, therefore, these findings could have high translational implications.