<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Sonnay, Sarah</dc:creator>
  <dc:creator>Poirot, Jordan</dc:creator>
  <dc:creator>Just, Nathalie</dc:creator>
  <dc:creator>Clerc, Anne-Catherine</dc:creator>
  <dc:creator>Gruetter, Rolf</dc:creator>
  <dc:creator>Rainer, Gregor</dc:creator>
  <dc:creator>Duarte, João M. N.</dc:creator>
  <dc:date>2018-03-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Astrocytes play an important role in glutamatergic neurotransmission, namely by  clearing synaptic glutamate and converting it into glutamine that is transferred back to  neurons. The rate of this glutamate–glutamine cycle (VNT) has been proposed to  couple to that of glucose utilization and of neuronal tricarboxylic acid (TCA) cycle. In  this study, we tested the hypothesis that glutamatergic neurotransmission is also  coupled to the TCA cycle rate in astrocytes. For that we investigated energy  metabolism by means of magnetic resonance spectroscopy (MRS) in the primary  visual cortex of tree shrews (Tupaia belangeri) under light isoflurane anesthesia at  rest and during continuous visual stimulation. After identifying the activated cortical  volume by blood oxygenation level-dependent functional magnetic resonance  imaging, 1H MRS was performed to measure stimulation-induced variations in  metabolite concentrations. Relative to baseline, stimulation of cortical activity for 20  min caused a reduction of glucose concentration by −0.34 ± 0.09 µmol/g (p &lt; 0.001),  as well as a −9% ± 1% decrease of the ratio of phosphocreatine-to-creatine (p &lt; 0.05).  Then 13C MRS during [1,6-13C]glucose infusion was employed to measure fluxes of  energy metabolism. Stimulation of glutamatergic activity, as indicated by a 20%  increase of VNT, resulted in increased TCA cycle rates in neurons by 12% (VTCAn, p  &lt; 0.001) and in astrocytes by 24% (VTCAg, p = 0.007). We further observed linear  relationships between VNT and both VTCAn and VTCAg. Altogether, these results  suggest that in the tree shrew primary visual cortex glutamatergic neurotransmission  is linked to overall glucose oxidation and to mitochondrial metabolism in both neurons  and astrocytes.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/306390</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/306390/files/rai_ano.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/glia.23259</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Glia. - 2018, vol. 66, no. 3, p. 477–491</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Astrocytic and neuronal oxidative metabolism are coupled to the rate of glutamate–glutamine cycle in the tree shrew visual cortex</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
