4.7 Article

Measuring glucose cerebral metabolism in the healthy mouse using hyperpolarized 13C magnetic resonance

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SCIENTIFIC REPORTS
卷 7, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41598-017-12086-z

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资金

  1. European Union's Horizon European Research Council (ERC Consolidator Grant) [682574]
  2. National Institutes of Health [EB 015908, RR02584, HL 034557]
  3. Cancer Prevention and Research Institute of Texas (CPRIT grants) [RP 101243, RP 140021]
  4. Swiss National Science Foundation [PP00P2_133562]
  5. Centre d'Imagerie BioMedicale (CIBM) of the UNIL
  6. Centre d'Imagerie BioMedicale (CIBM) of the UNIGE
  7. Centre d'Imagerie BioMedicale (CIBM) of the HUG
  8. Centre d'Imagerie BioMedicale (CIBM) of the CHUV
  9. Centre d'Imagerie BioMedicale (CIBM) of the EPFL
  10. Leenards Foundation
  11. Jeantet Foundation
  12. European Research Council (ERC) [682574] Funding Source: European Research Council (ERC)

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The mammalian brain relies primarily on glucose as a fuel to meet its high metabolic demand. Among the various techniques used to study cerebral metabolism, C-13 magnetic resonance spectroscopy (MRS) allows following the fate of C-13-enriched substrates through metabolic pathways. We herein demonstrate that it is possible to measure cerebral glucose metabolism in vivo with sub-second time resolution using hyperpolarized C-13 MRS. In particular, the dynamic C-13-labeling of pyruvate and lactate formed from C-13-glucose was observed in real time. An ad-hoc synthesis to produce [2,3,4,6,6-H-2(5), 3,4-C-13(2)]-D-glucose was developed to improve the 13C signal-to-noise ratio as compared to experiments performed following [U-H-2(7), U-C-13]-D-glucose injections. The main advantage of only labeling C3 and C4 positions is the absence of C-13-C-13 coupling in all downstream metabolic products after glucose is split into 3-carbon intermediates by aldolase. This unique method allows direct detection of glycolysis in vivo in the healthy brain in a noninvasive manner.

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