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

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.


Introduction
Diabetes mellitus (DM) is a pandemic metabolic problem characterized by hyperglycemia due to defects in secretion or action of insulin, namely, type 1 or type 2 diabetes mellitus (T2DM), respectively. In 2015, 415 million people had DM in the world, and the number will grow to 522 million in 2030 with the conservative estimation [1,2]. High-fat diet (HFD) is one leading cause of T2DM [3,4], causing resistance to insulin in multiple organs [5]. e relatively subtle metabolic changes, such as moderate hyperglycemia and increased plasma triglyceride (TG) levels, can gradually lead to structural changes and heart failure [6,7]. Some previous reports have shown that the myocardium of humans and animals with T2DM might switch energy production from glucose utilization to fatty acid oxidation [8][9][10], which may play a critical role in the pathogenesis of T2DM. e presence of hyperinsulinemia, obesity, and impaired glucose tolerance in the rats with HFD has been characterized as the prediabetic T2DM rat model in the literature [11]. e Randle cycle (glucose fatty-acid cycle), a metabolic process involving the switch between glucose and fatty acids for substrates [12], is theorized to play a role in explaining T2DM and IR [13,14]. Although the energy balance from differing macronutrient composition is equal, the glucose and fat balances that contribute to the overall energy balance are supposed to change reciprocally with dietary composition [15]. Monitoring the metabolic switch in myocardium would help in early detection and treatment of the myocardial changes in T2DM.
Cardiac magnetic resonance (CMR) imaging is a noninvasive assessment of both ischemic and nonischemic heart disease and heart failure [16]. CMR has become the gold standard for evaluating the left ventricular (LV) function, providing objective structural and detailed functional readouts [17][18][19]. However, the measurement of myocardial metabolism remains a challenge for CMR. 18 F-fluorodeoxyglucose ( 18 F-FDG) is a glucose analog which has been extensively used in positron emission tomography (PET) in clinical oncological diagnosis and assessment of the treatment response [20]. 18 FDG is taken up by cells and trapped in the cytoplasm as 18 F-FDG-6-phosphate by hexokinase once it enters into cells through glucose transporters (Glut) [21]. Normal myocardium also actively uptakes 18 F-FDG due to high expression of hexokinase 2 [22,23], providing the opportunity of using 18 F-FDG to probe the first command step of myocardium glucose utilization by the in vivo noninvasive micro-PET study.
e Langendorff system perfused with carbon-13-labeled glucose ([U-13 C]Glc) can potentially probe the downstream metabolic activities further to 18 F-FDG-6-phosphate in the myocardium [5]. High-resolution nuclear magnetic resonance (NMR) technology can identify the following metabolic products of [U-13 C]Glc to precisely characterize the myocardial glucose utilization in the HFD-induced insulin resistance (IR). However, noninvasive detection of early myocardial changes of the prediabetic T2DM rat model has not been investigated yet.
We aim to characterize the metabolic changes associated with myocardial glucose utilization in a rat model of HFDinduced IR as an early diabetic onset model using the noninvasive imaging of cardiac MRI, 18 F-FDG micro-PET, and [U-13 C]Glc NMR corroboration.

Animal Model and Experiment Design.
We purchased male Sprague-Dawley (SD) rats (age 6 weeks) from BioLASCO Taiwan Co., Ltd. (Taipei, Taiwan). e SD rats were maintained in a climate-controlled facility on a 12 h light/12 h dark cycle with access to water and food ad libitum. All experimental procedures were conducted according to the Guide for the Care and Use of Laboratory Animals and were approved by the Institutional Animal Care and Use Committee of Chang Gung University and Chang Gung Memorial Hospital, Taiwan (IACUC: CGU13-051). After two weeks of acclimation, the SD rats were randomly assigned to 2 groups, fed a regular chow diet (control, C; n � 9) or high-fat diet (HFD; n � 9) ad libitum for 10 weeks. As our previous research, the regular chow diet consisted of 23.5% protein, 5.1% fat, and 50.3% carbohydrates (g %, LabDiet ® 5001, St. Louis, MO); the HFD consisted of 24% protein, 24% fat, and 41% carbohydrates (g %, Research Diets D12451I, New Brunswick, NJ) [24]. We recorded their body weight and food intake weekly. In the SD rats (C, n � 9 ; HFD, n � 9), blood from the tail vein was withdrawn under fasting status for insulin-resistant testing. e biochemistry indexes, such as triacylglycerol (TG), total cholesterol (T-CHO), and highdensity lipoprotein (HDL-C), were detected by Fujifilm NX500i (Japan) with 10 μl of plasma following the ELISA kit protocol. e measurement ranges of glucose, TG, T-CHO, and HDL-C are 19.62-600 mg/dL, 10-500 mg/dL, 50-450 mg/dL, and 10-110 mg/dL, respectively. Homeostasis model assessment-insulin resistance (HOMA-IR) was calculated using HOMA2 calculator [25] and has been reported as a useful tool for diagnosing insulin resistance [26]. We carried out cardiac MRI weekly for 10 weeks (Control, n � 9; HFD, n � 9) and 18 F-FDG PETon week 1, week 4, and week 7 (Control, n � 3; HFD, n � 3) after HFD feeding. We further analyzed the heart by using the [U-13 C]Glc Langendorff perfusion study, NMR, and western blotting at 18 weeks of age (Control, n � 2; HFD, n � 3). In comparison to the early phase of pre-DM status, we analyzed the hearts with and without Langendorff perfusion by NMR and western blotting at 32 weeks of age (Control, n � 3; HFD, n � 3), as detailed below. e flow chart of the performing animal and tissue experiments was summarized in Figure 1.

CMR.
CMR was performed with ECG and respiratory gating on the ClinScan 7T MRI (Bruker BioSpin, Germany). Short-axis CINE with the bright-blood technique was chosen to capture myocardial wall motion and thickness between end-systole and end-diastole phases. Specific parameters of CINE using FLASH sequence are TR/TE 12/1.67 ms, slice thickness 1 mm, three averages, flip angle 15°, the field of view 45 × 45 mm 2 , and 144 × 192 matrix, which gives rise to in-plane resolution 0.312 × 0.234 mm 2 . Such CINE scans were acquired sequentially and evenly from the base to the apex, yet the slice numbers to cover the whole heart and the corresponding acquisition time per incidence slightly varied among different animals and ECG stability. All CINE frames were quantitatively analyzed using QMass (Medis, the Netherlands), with manual delineation of the myocardium for left ventricular volume, ejection fraction, wall motion, and wall thickness.

Micro-PET.
e SD rats were imaged using an InveonTM system (Siemens Medical Solutions Inc., Malvern, PA, USA) at Chang Gung Memorial Hospital, Taiwan. All rats were fasted for 12 hours before micro-PET but allowed ad libitum to access water. Although the blood glucose level of each rat was not measured before the micro-PET study, in the previous reports, there is no significant difference in glucose levels of the control and HFD rats with 12-hour fasting [27]. e rats underwent a 30 min image acquisition in the prone position 90 min after receiving 22.49 ± 0.17 (standard deviation, SD) MBq of 18 F-FDG via tail vein injection. e rats were anesthetized with 3% isoflurane, and the heart of the rat was positioned near the center of the field of view where the spatial resolution is approximately 1.2 mm. e regions of interest (ROIs) of the myocardium were analyzed in the PET images manually. e 18 F-FDG uptakes of the myocardium were expressed as the maximum standardized uptake value (SUV max ) [28]. All image analyses were conducted by using PMOD version 3.2 image analysis software (PMOD Technologies Ltd., Zurich, Switzerland).

Isolated Heart
Perfusion. Rats were anesthetized with sodium pentobarbitone (50 mg/kg, intraperitoneal injection, IP) and given heparin (300 units/kg, IP), following a cervical dislocation. Immediately, hearts were isolated in ice-cold Krebs-Henseleit buffer [21], cannulated via the aorta, and perfused in Langendorff mode at a constant perfusion pressure of 100 mmHg at 37°C [29]. Hearts were perfused with KH buffer (137.0 mM NaCl, 5.4 mM KCl, 1.22 mM MgSO 4 , 1.8 mM CaCl 2 , 1.2 mM KH 2 PO 4 , 11.0 mM dextrose, and 6.0 mM HEPES, pH 7.4), gassed with 95% O 2 and 5% CO 2 in steady perfusion for 10 min. en, the dextrose in KH buffer was replaced with [U-13 C]Glc, following 2 min perfusion. e hearts were removed from the Langendorff perfusion system after completing the perfusion, and each compartment of the heart was separated at the saline cooling bath. Each compartment of the hearts was wrapped in an aluminum foil and stored in liquid nitrogen for further usage.

NMR Metabolomic Study and Data
Analysis. NMR spectra were acquired using a Bruker Avance III HD 600 MHz spectrometer operating at 600.13 MHz and equipped with a TXI CryoProbe at 300 K. Two types of 1 H NMR spectra were acquired: NOESY and Carr-Purcell-Meiboom-Gill (CPMG) pulse sequence. e analyzed aqueous metabolites were glucose, lactate, acetate, glutamine, and glutamate; the analyzed lipophilic metabolite was a long-chain lipid component (CH 2 ) n. Using the Bruker TopSpin 3.2 software and Chenomx Profiler 8.0, we integrated the NMR spectra for the HFD and control groups. e ratio of the metabolic concentrations of HFD and control groups at 18 and 32 weeks was determined, respectively. e metabolic levels of the NMR spectra were computed by the internal reference of sodium 3-trimethylsilyl-2,2,3,3-tetradeuteropropionate (TSP) in the aqueous phase and of tetramethylsilane (TMS) in the lipophilic phase. e sum of 13 C resonances at the 4th and 5th positions of glutamate was compared with the sum of 13 C resonances at the 1st, 2nd, and 3rd positions (Glu45/Glu123 ratio).

Western
Blotting. Myocardium lysates were analyzed by western blotting, as described previously [30]. e myocardium lysate protein was transferred onto Immun-Blot PVDF membranes (Bio-Rad, USA). PVDF membranes were . e membranes were then incubated with the anti-rabbit or anti-mouse secondary antibody (Sigma-Aldrich, Israel). Specific binding antibody-target protein interactions were rinsed with ECL (BioRad, USA) and detected under the chemiluminescence system (BioSpectrum UVP, CA, USA). Each blotting band was normalized with its loading control and quantitated utilizing ImageJ 1.49t.

Statistical Analysis.
Values are expressed as means ± SD (standard deviation). Statistical analyses were performed using Prism Software (version 6; GraphPad). Data were not normally distributed based on the Kolmogorov-Smirnov test.  Figure 2: Characterization of HFD-induced obesity model. Rats fed high-fat diet became significantly obese in the time course of body weight (a). Slightly increased glucose concentration in plasma in the HFD group after 10 weeks of high-fat diet feeding (b). Significantly increased insulin (c), HOMA-IR (d), triglyceride (e), and total cholesterol (f ) concentration in the HFD group after 10 weeks of high-fat diet feeding. Slightly decreased HDL-C in the HFD group after 10 weeks of high-fat diet feeding (g). Taken together, the HFD rats developed insulin resistance in 10 weeks after high-fat diet feeding. * P < 0.05; * * P < 0.01; * * * P < 0.001 versus control. erefore, the cardiac uptakes in the control and HFD groups were compared using Kruskal-Wallis analysis followed by the nonparametric Tukey test. In other experimental data, the comparison of control and HFD groups was done by Student's t-test with nonparametric Mann-Whitney test. A P value of 0.05 or less was considered statistically significant.

Physiological and Hemodynamics Remodeling in HFD-
Induced IR Hearts. After diet alteration for 10 weeks, rats fed HFD developed a phenotype of IR syndrome, which is characterized by hyperlipidemia and hyperinsulinemia and impaired fasting glucose and homeostasis model assessment-insulin resistance (HOMA-IR), as shown in Figure 2. e values of HOMA-IR were obtained by means of the HOMA2 calculator. e body weight, blood insulin concentration, HOMA-IR, triglyceride, and total cholesterol significantly increased in the HFD group (P < 0.05), as compared with the control group.

Morphological Effect of HFD on CMR.
e representative short axis of CMR images in end-systolic and end-diastolic phases in the control and the HFD rats at 16 weeks of age is demonstrated in Figure 3. In vivo cardiac function of control and HFD groups was summarized by CMR with QMass analysis and pool analysis comparison in Table 1. Rats with HFD have a higher ejection fraction, smaller left ventricular end-systolic volume (LVESV), and thicker end-systolic wall thickness than the control group (P < 0.05). 18 F-FDG PET. HFD rats have altered in vivo myocardial 18 F-FDG uptakes. e SUV max of the left ventricular myocardium was significantly increased in the HFD group than that in the control group over time periods. (SUV max , 1.71 ± 0.36 versus 1.22 ± 0.16 at week 1; 2.18 ± 0.39 versus 0.92 ± 0.05 at week 4, P � 0.0049; 2.00 ± 0.93 versus 1.10 ± 0.08 at week 7), as shown in Figure 4. 18 F-FDG can be taken up by glycolytic cells and phosphorylated by hexokinase but was trapped in the cells in its phosphorylated form, due to lacks of a 2′ hydroxyl group needed for subsequent metabolism [31]. erefore, we used [U-13 C] Glc NMR to further study the downstream metabolism of myocardium glucose utilization.

High-Resolution NMR Analysis of [U-13 C]Glc Perfused Myocardium.
ere is a list of the steady-state aqueous metabolites associated with the glucose metabolic pathway of the HFD and control rat hearts by 1 H NMR spectrum analyses in Supplementary Material 1. e majority of myocardial metabolites maintained stable as compared with controls, except levels of acetate, butyrate, glutamine, O-acetylcarnitine, propionate, taurine, and uridine significantly decreased in the HFD groups compared to the control group (P < 0.05). ose altered levels of metabolites such as acetate, butyrate, and glutamine were associated with the pathways of glucose metabolism. Other altered levels of metabolites, O-acetylcarnitine, propionate, taurine, and uridine were related to the pathway of fatty acid metabolism. To further interrogate the increased glucose uptake demonstrated on 18 F-FDG PET, glucose tracers labeled at each carbon position [U-13 C]Glc was infused into the Langendorff perfusion system, to analyze the glucose utility of the HFD. Figure 5 reveals the glucose metabolic network identified by the [U-13 C]Glc NMR system. In myocardium glucose utilization, the 13 C-carbon of glucose was metabolized to glycine (Gly), lactate, and pyruvate as well as acetyl-CoA. e 13 Ccarbon from acetyl-CoA was contained in citrate, isocitrate, and α-ketoglutarate (αKG), which synthesizes glutamic acid and glutamine (Gln). e 13 C-carbon at the 4th and 5th positions of glutamine indicates the utility of [U-13 C]Glc undergoing oxidative phosphorylation via the TCA cycle. e Glu45/Glu123 ratio of labeled 13 C-carbon in glucose metabolic substances of HFD groups is significantly higher than that of control groups (18 weeks of age: 0.38 ± 0.03 versus 0.33 ± 0.01; 32 weeks of age: 1.06 ± 0.28 versus 0.39 ± 0.07, P � 0.017).

Myocardial Overexpression of Glut4, PARP, and LC3B in HFD-Induced IR.
Interestingly, we found the protein expression of Glut4 increased in accordance with the change on the 18 F-FDG PET (P < 0.05). e mRNA levels for Glut4 (Slc2a4 gene) were also altered (P < 0.05). e different trends in mRNA and protein expression might indicate a complex feedback mechanism and warrant further study. e AceCS1 protein and ACSS2 mRNA expression were not significantly changed during both the early and late HFD feeding. However, in 18 weeks of age rat myocardium, the PARP expression was significantly increased as compared with the control (P < 0.05), following to 32 weeks of age, the PARP expression was decreased (early versus late, P < 0.05).

Contrast Media & Molecular Imaging
Notably, the expression of LC3B, an autophagy activation protein, was higher in the 32 weeks of age HFD group compared with the control (P < 0.05) ( Figure 6).

Discussion
In the present study, we found the HFD rats in 10 weeks high-fat diet feeding results in mild hyperglycemia, hypercholesterolemia, hyperinsulinemia, and homeostasis model assessment-IR (HOMA-IR), as determined by the biochemical and physiological analysis, with a significant increase in body weight. e significantly increased EF and decreased LVEDV was measured in the HFD rats, indicating that the ten-week HFD fed rats might develop the myocardial hypertrophy, observed as the thicker myocardium wall by CMR. Corresponding to 18 F-FDG PET study, the myocardium walls of the HFD rats show significant 18 F-FDG uptake among seven weeks, implying that the HFD rats need amounts of glucose to acquire the energy to support the hypertrophic myocardium activities under glucose utilization in the early stage. Also, with increased glucose metabolite, for example, glutamine and glutamate, and Glut4 expression in late stage, the highly increased myocardium glucose utilization in HFD rats should fully be demonstrated as taking the results together.
We noticed that blood glucose levels between control and high-fat diet groups did not different significantly, Values are expressed as mean ± SD. e cardiac function of the control and HFD rats was measured from CMR images and QMass Software; * P < 0.05 and * * P < 0.01 versus control; LV � left ventricle; ED � end-diastolic volume; ES � end-systolic volume. which might be attributed to our fasting procedure that is not strict. Even though we removed their food from cages, rats still could eat the bedding materials, fests, and food debris remaining in the cages. Our observations were in line with reports showing no significant difference in glucose levels between control and high-fat diet feeding rats for 9 weeks [32] and 16 weeks [33]. Our results detailed how the Randel cycle replenishes the intermediates of the citric acid cycle. e hemodynamic stress of HFD-induced myocardium overrides fatty acid inhibition of glucose metabolism, which is presumably associated with activation of AMP-activated protein kinase (AMPK), an immediate metabolic adaption and protects the heart from ischemic stress [34]. Interestingly, some previous studies reported that myocardial IR induced by HFD feeding preserves the cardiac contractile function in mild to moderate heart failure rats [35]. Histopathological analysis of the crosssectional area of myocardium showed significantly increased thickness in HFD rats [24]. We showed that the myocardial hypertrophy induced by HFD needs to consume more energy to support its activity and function by glycose utilization. In line with our results, the increase in myocardial glucose utilization rate compensates the poor fatty acid uptake in the rats with spontaneously hypertension or myocardial infarction [36,37]. Due to the disturbance in cardiac metabolism, the HFD results in the hyperinsulinemia and hemodynamics remodeling in the pre-T2DM rat model. On the contrary, the cardiomyocytes cross-sectional area increased in the long-term HFD feeding mice [38]. In another mice study with a prolonged HFD for 20 weeks, there was a 40% increase in fatty acid oxidation in the myocardium, whereas glucose oxidation was decreased to 30% of the control [39]. Contrary to our pre-T2DM rat model, the diabetic mouse model appears to be a different metabolic phenotype of cardiopathology.
Some previous reports have demonstrated the alteration of myocardial metabolism in the various diabetic rat models [11]. Shoghi et al. found the decreased myocardial glucose uptake rate in PET images and lower expression of glucose transporters (Glut1 and Glut4) in 20-week-old Zucker Diabetic Fatty (ZDF) rats (fa/fa) but did not show significant difference in morphological changes in the echocardiography measurements [40]. Feeding Wistar rats with high-fat and high-fructose diet for 16 weeks with a small dose of streptozotocin, Menard et al. reported altered myocardium energy metabolism as well as increased myocardial nonesterified fatty acid uptake in the 14 (R, S)-18 F-fluoro-6-thiaheptadecanoic acid ( 18 F-FTHA) micro-PET images [41]. e above evidence supports the metabolic alterations in the myocardium during the development of T2DM. 18 F-FDG PET demonstrated an early alternation of myocardium glucose utilization in 4-week HFD, whereas the myocardium dysfunction of HFD rats was detected by CMR after 18-week HFD. It seems to be reasonable that the perturbation of myocardium metabolism is followed by the myocardium dysfunction over the progression of the insulin-induced cardiopathological diseases. We have shown the myocardium glucose utilization by in vivo glucose analogs PET tracer and ex vivo labeling [U-13 C]Glc NMR. More recent reports suggested the glutamine as a vital biomarker of metabolic syndromes and insulin-resistant phenotypes [42,43]. e mice fed oral supplementation of glutamine leading to reduced glucose concentration, indicating glutamine, may play a critical role in the metabolic disease pathways. In our study, we showed that the ratio of labeled C4-5 to C1-3 in glutamine in HFD mice hearts increases, implying either increased Glu 45 or decreased Glu 123 . Glu 45 is from [U-13 C]Glc; Glu 123 can be from glutamine uptake, which did not occur in our study. e increased glutamine concentration in HFD mice myocardium could be a positive feedback mechanism as the myocardium suffers from the metabolic problem. e further mechanism of glutamine feedback warrants validations in the future. Furthermore, the myocardium fatty acid is considered to predominate the metabolism in the diabetic heart diseases prevailing, which has not been discussed in our study. Even so, several published literature have investigated the myocardium energy utilization by PET radiopharmaceuticals such as carbohydrate metabolism ( 18 F-FDG, 11 C-acetate, and 11 C-glucose) and fatty acid metabolism ( 11 C-palmitate and fatty acid analogs) [44]. e multiple metabolic substrates PET tracers could be our further study direction to investigate the myocardium energy utilization and metabolism.
Cardiac health relies on the heart's ability to utilize different substrates to support overall oxidative metabolism to generate ATP. We demonstrated overexpressed Glut4 and associated changes in mRNA levels in the HFD group, which linked to an increased autophagy activity protein that might intent to generate the additional ATP to support the excessed myocardium activities from the cardiac hypertrophy of HFD rats. e switch from glucose to fatty acid oxidation leads to a less-efficient oxidative phosphorylation because more electrons transported to complex 2 rather than complex 1 in the mitochondrial respiratory chain, hence increasing the production of ROS. Our study represented the early metabolic adaptation of myocardium induced by HFD. e identification of the metabolic phenotypes of chronic diseases including diabetics and heart failure in an early period facilitates the improvement of therapeutic impact [34]. e presence of pre-DM IR associated with a higher reliance on myocardial glucose metabolism. e perturbations in myocardial metabolism may precede an eventual decline of the left ventricular function. Future research should explore the influence of pre-DM status on clinical cardiac 18 F-FDG PET imaging to better stratify patients for suitable therapeutic intervention.

Limitations
ere are limitations to this study. First, the obese and T2DM heart is less adaptable to myocardial substrate metabolism under anesthesia, known as anesthesia-induced cardioprotection [45]. Anesthesia is unavoidable during in vivo imaging study, and the impact to experimental results still under debate [45,46]. erefore, a minimum dose of anesthesia was considered as a concession in our study. Instead of using a continuous dynamic scan, our micro-PET study was acquired 30 min as a static scan, not only keeping conscious during the uptake period but also less time-consuming to adapt clinical situation. For this purpose, we had decided to omit the metabolic rate of glucose with 18 F-FDG derived from dynamic PET scan and Patlak analysis. Nevertheless, we used a clinical standard quantitative SUV of the myocardium to reflect analog glucose uptake in the regional organs [28]. e glucose utilization is increased in the early HFDinduced myocardial adaptation in the pre-T2DM model, in contrast to the glucose metabolism transit to fatty acid metabolism for energy utility in the myocardium in the late T2DM. Although the preliminary report demonstrated the potential to quantify the myocardial triglyceride content using CMR spectroscopy [47], CMR spectroscopy suffered from the limited sensitivity to detect the glycolysis pathway and was not chosen in this study. 18 F-FDG, although being transported into the myocardium and phosphorylated by hexokinase as the first step toward glycolysis, is trapped intracellularly as 18 F-FDG-6phosphate, thus cannot track down the downstream glycolytic pathway. erefore, we applied a combination approach of 18 F-FDG and [U-13 C]Glc NMR metabolomic analysis trying to understand the whole metabolic landscape. Nevertheless, it is the first time that the downstream metabolic products of pyruvate can be monitored by imaging the augmented form of CMR-hyperpolarized [1-13 C] pyruvate in real time, and hopefully, these promising results found in this study will have clinical applications in the near future [48].

Conclusions
In conclusion, HFD-induced IR induces cardiac morphological changes, with a higher ejection fraction, smaller  Figure 6: Western blotting and mRNA analysis of myocardium: AceCS1, Glut4, PARP, and LC3B protein expression and Slc2a4 and Acss2 gene expression in the perfusion hearts in HFD and control rats in 18 weeks and 36 weeks after high-fat diet feeding. AceCS1 protein expression and Acss2 gene expression did not show a significant difference between control and HFD in early and late stages. However, mRNA levels change in Glut4, albeit different in trend. Nonetheless, the protein expression of Glut4 increases in accordance with the 18 F-FDG PET/CT. Decreased cleaved/prototype PARP and increased LC3B-autophagy activation in the myocardium of the HFD rats are noted.
LVESV, and thicker end-systolic wall thickness than the control group. e prediabetic myocardium increased glucose utility undergoing oxidative phosphorylation via the TCA cycle, supported by overexpression of glucose tranporters and acetyl-CoA synthase. Noninvasive imaging biomarker has potentials in detecting the metabolic perturbations prior to the decline of the left ventricular function.

Data Availability
e NMR, western blot, and mRNA data used to support the findings of this study are available from the corresponding author upon reasonable request. e CMR and PET scan images data used to support the findings of this study are available from Yi-Hsiu Chung upon reasonable request.

Conflicts of Interest
e authors declare that there are no conflicts of interest regarding the publication of this article.