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PET CMRglc mapping and 1H-MRS show altered glucose uptake and neurometabolic profiles in BDL rats

Published inAnalytical biochemistry, vol. 647, 114606
Publication date2022-06-15
First online date2022-03-01
Abstract

Type C hepatic encephalopathy (HE) is a complex neuropsychiatric disorder occurring as a consequence of chronic liver disease. Alterations in energy metabolism have been suggested in type C HE, but in vivo studies on this matter remain sparse and have reported conflicting results. Here, we propose a novel preclinical18F-FDG PET methodology to compute quantitative 3D maps of the regional cerebral metabolic rate of glucose (CMRglc) from a labelling steady-state PET image of the brain and an image-derived input function. This quantitative approach shows its strength when comparing groups of animals with divergent physiology, such as HE animals. PET CMRglcmaps were registered to an atlas and the mean CMRglcfrom the hippocampus and the cerebellum were associated to the corresponding localized1H MR spectroscopy acquisitions. This study provides for the first time local and quantitative information on both brain glucose uptake and neurometabolic profile alterations in a rat model of type C HE. A 2-fold lower brain glucose uptake, concomitant with an increase in brain glutamine and a decrease in the main osmolytes, was observed in the hippocampus and in the cerebellum. These novel findings are an important step towards new insights into energy metabolism in the pathophysiology of HE.

Keywords
  • (1)H MRS
  • (18)F-FDG PET
  • Bile duct ligation
  • Cerebral metabolic rate of glucose
  • Rat brain
  • Type C hepatic encephalopathy
  • Animals
  • Brain / diagnostic imaging
  • Brain / metabolism
  • Glucose / metabolism
  • Glutamine / metabolism
  • Hepatic Encephalopathy / metabolism
  • Proton Magnetic Resonance Spectroscopy
  • Rats
Citation (ISO format)
MOSSO, Jessie et al. PET CMRglc mapping and 1H-MRS show altered glucose uptake and neurometabolic profiles in BDL rats. In: Analytical biochemistry, 2022, vol. 647, p. 114606. doi: 10.1016/j.ab.2022.114606
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Article (Published version)
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Journal ISSN0003-2697
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Creation23/11/2023 08:13:51
First validation23/11/2023 16:25:17
Update19/09/2025 10:08:58
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