Early Imaging Biomarker of Myocardial Glucose Adaptations in High-Fat-Diet-Induced Insulin Resistance Model by Using 18F-FDG PET and [U-13C]glucose Nuclear Magnetic Resonance Tracer

Contrast Media Mol Imaging. 2018 Jul 12:2018:8751267. doi: 10.1155/2018/8751267. eCollection 2018.

Abstract

Background: High-fat diet (HFD) induces systemic insulin resistance leading to myocardial dysfunction. We aim to characterize the early adaptations of myocardial glucose utility to HFD-induced insulin resistance.

Methods: Male Sprague-Dawley rats were assigned into two groups, fed a regular chow diet or HFD ad libitum for 10 weeks. We used in vivo imaging of cardiac magnetic resonance (CMR), 18F-FDG PET, and ex vivo nuclear magnetic resonance (NMR) metabolomic analysis for the carbon-13-labeled glucose ([U-13C]Glc) perfused myocardium.

Results: As compared with controls, HFD rats had a higher ejection fraction and a smaller left ventricular end-systolic volume (P < 0.05), with SUVmax of myocardium on 18F-FDG PET significantly increased in 4 weeks (P < 0.005). The [U-13C]Glc probed the increased glucose uptake being metabolized into pyruvate and acetyl-CoA, undergoing oxidative phosphorylation via the tricarboxylic acid (TCA) cycle, and then synthesized into glutamic acid and glutamine, associated with overexpressed LC3B (P < 0.05).

Conclusions: HFD-induced IR associated with increased glucose utility undergoing oxidative phosphorylation via the TCA cycle in the myocardium is supported by overexpression of glucose transporter, acetyl-CoA synthase. Noninvasive imaging biomarker has potentials in detecting the metabolic perturbations prior to the decline of the left ventricular function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism*
  • Carbon Isotopes / chemistry*
  • Diet, High-Fat
  • Disease Models, Animal
  • Fluorodeoxyglucose F18 / chemistry*
  • Glucose / metabolism*
  • Glucose Transporter Type 4 / metabolism
  • Hemodynamics
  • Insulin Resistance*
  • Magnetic Resonance Spectroscopy*
  • Male
  • Microtubule-Associated Proteins / metabolism
  • Myocardium / metabolism*
  • Obesity / pathology
  • Obesity / physiopathology
  • Poly(ADP-ribose) Polymerases / metabolism
  • Positron-Emission Tomography*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats, Sprague-Dawley

Substances

  • Biomarkers
  • Carbon Isotopes
  • Glucose Transporter Type 4
  • LC3 protein, rat
  • Microtubule-Associated Proteins
  • RNA, Messenger
  • Fluorodeoxyglucose F18
  • Poly(ADP-ribose) Polymerases
  • Carbon-13
  • Glucose