Evaluation of Hepatic Glucose and Palmitic Acid Metabolism in Rodents on High-Fat Diet Using Deuterium Metabolic Imaging

Viktoria Ehret; Usevalad Ustsinau; Joachim Friske; Thomas Scherer; Clemens Fürnsinn; Thomas H Helbich; Cécile Philippe; Martin Krššák

doi:10.1002/jmri.29437

Evaluation of Hepatic Glucose and Palmitic Acid Metabolism in Rodents on High-Fat Diet Using Deuterium Metabolic Imaging

J Magn Reson Imaging. 2024 May 9. doi: 10.1002/jmri.29437. Online ahead of print.

Authors

Viktoria Ehret¹, Usevalad Ustsinau², Joachim Friske³, Thomas Scherer¹, Clemens Fürnsinn¹, Thomas H Helbich³, Cécile Philippe², Martin Krššák¹

Affiliations

¹ Division of Endocrinology and Metabolism, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
² Division of Nuclear Medicine, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, Vienna, Austria.
³ Division of Molecular and Structural Preclinical Imaging, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, Vienna, Austria.

PMID: 38721871
DOI: 10.1002/jmri.29437

Abstract

Background: One of the main features of several metabolic disorders is dysregulation of hepatic glucose and lipid metabolism. Deuterium metabolic imaging (DMI) allows for assessing the uptake and breakdown of ²H-labeled substrates, giving specific insight into nutrient processing in healthy and diseased organs. Thus, DMI could be a useful approach for analyzing the differences in liver metabolism of healthy and diseased subjects to gain a deeper understanding of the alterations related to metabolic disorders.

Purpose: Evaluating the feasibility of DMI as a tool for the assessment of metabolic differences in rodents with healthy and fatty livers (FLs).

Study type: Animal Model.

Population: 18 male Sprague Dawley rats on standard (SD, n = 9, healthy) and high-fat diet (HFD, n = 9, FL disease).

Field strength/sequence: Phase-encoded 1D pulse-acquire sequence and anatomy co-registered phase-encoded 3D pulse-acquire chemical shift imaging for ²H at 9.4T.

Assessment: Localized and nonlocalized liver spectroscopy was applied at eight time points over 104 minutes post injection. The obtained spectra were preprocessed and quantified using jMRUI (v7.0) and the resulting amplitudes translated to absolute concentration (mM) according to the ²H natural abundance water peak.

Statistical tests: Two-way repeated measures ANOVA were employed to assess between-group differences, with statistical significance at P < 0.05.

Results: DMI measurements demonstrated no significant difference (P = 0.98) in the uptake of [6,6'-²H₂]glucose between healthy and impaired animals (AUC_SD = 1966.0 ± 151.5 mM - minutes vs. AUC_HFD = 2027.0 ± 167.6 mM·minutes). In the diseased group, the intrahepatic uptake of palmitic acid d-31 was higher (AUC_HFD = 57.4 ± 17.0 mM·minutes, AUC_SD = 33.3 ± 10.5 mM·minutes), but without statistical significance owing to substantial in-group variation (P = 0.73).

Data conclusion: DMI revealed higher concentrations of palmitic acid in rats with FL disease and no difference in hepatic glucose concentration between healthy and impaired animals. Thus, DMI appears to be a useful tool for evaluating metabolism in rodents with FL disease.

Level of evidence: 2 TECHNICAL EFFICACY: Stage 3.

Keywords: deuterium metabolic imaging; fatty acids; fatty liver; glucose; metabolism.

Abstract

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