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ABSTRACT: Introduction
Type C hepatic encephalopathy (HE) is a decompensating event of chronic liver disease leading to severe motor and cognitive impairment. The progression of type C HE is associated with changes in brain metabolite concentrations measured by 1H magnetic resonance spectroscopy (MRS), most noticeably a strong increase in glutamine to detoxify brain ammonia. In addition, alterations of brain cellular architecture have been measured ex vivo by histology in a rat model of type C HE. The aim of this study was to assess the potential of diffusion-weighted MRS (dMRS) for probing these cellular shape alterations in vivo by monitoring the diffusion properties of the major brain metabolites.Methods
The bile duct-ligated (BDL) rat model of type C HE w
SUBMITTER: Mosso J
PROVIDER: S-EPMC10987698 | biostudies-literature | 2024
REPOSITORIES: biostudies-literature