Cardiac metabolic modulation upon low-carbohydrate low-protein ketogenic diet in diabetic rats studied in vivo using hyperpolarized 13 C pyruvate, butyrate and acetoacetate probes

Diabetes Obes Metab. 2019 Apr;21(4):949-960. doi: 10.1111/dom.13608. Epub 2019 Jan 13.

Abstract

Aim: To investigate the effects of long-term low-carbohydrate low-protein ketogenic diet (KD) on cardiac metabolism and diabetic cardiomyopathy status in lean diabetic Goto-Kakizaki (GK) rats.

Materials and methods: Diabetic GK rats were fed with KD for 62 weeks. Cardiac function and metabolism were assessed using magnetic resonance imaging and 13 C magnetic resonance spectroscopy (13 C-MRS), at rest and under dobutamine stress. 13 C-MRS was performed following injection of hyperpolarized [3-13 C]acetoacetate, [1-13 C]butyrate or [1-13 C]pyruvate to assess ketone body, short-chain fatty acid or glucose utilization, respectively. Protein expression and cardiomyocyte structure were determined via Western blotting and histology, respectively.

Results: KD lowered blood glucose, triglyceride and insulin levels while increasing blood ketone body levels. In KD-fed diabetic rats, myocardial ketone body and glucose oxidation were lower than in chow-fed diabetic rats, while myocardial glycolysis and short-chain fatty acid oxidation were unaltered. Dobutamine stress revealed an increased cardiac preload and reduced cardiac compliance in KD-fed diabetic rats. Dobutamine-induced stimulation of myocardial glycolysis was more enhanced in KD-fed diabetic rats than in chow-fed diabetic rats, which was potentially facilitated via an upregulation in basal expression of proteins involved in glucose transport and glycolysis in the hearts of KD-fed rats. The metabolic profile induced by KD was accompanied by cardiac hypertrophy, a trend for increased myocardial lipid and collagen content, and an increased marker of oxidative stress.

Conclusion: KD seems to exacerbate diabetic cardiomyopathy in GK rats, which may be associated with maladaptive cardiac metabolic modulation and lipotoxicity.

Keywords: 13C magnetic resonance spectroscopy; diabetes; hyperpolarized 13C substrates; ketogenic diet; myocardial substrate metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetoacetates
  • Animals
  • Blood Glucose / metabolism
  • Butyrates
  • Carbon-13 Magnetic Resonance Spectroscopy
  • Cardiotonic Agents
  • Diabetes Mellitus / metabolism*
  • Diabetic Cardiomyopathies / metabolism
  • Diabetic Cardiomyopathies / pathology
  • Diet, Carbohydrate-Restricted
  • Diet, Ketogenic*
  • Diet, Protein-Restricted*
  • Dobutamine
  • Fatty Acids, Volatile / metabolism
  • Glucose / metabolism*
  • Glycolysis
  • Insulin / metabolism
  • Ketone Bodies / metabolism*
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Myocytes, Cardiac / metabolism*
  • Myocytes, Cardiac / pathology
  • Pyruvic Acid
  • Rats
  • Triglycerides / metabolism

Substances

  • Acetoacetates
  • Blood Glucose
  • Butyrates
  • Cardiotonic Agents
  • Fatty Acids, Volatile
  • Insulin
  • Ketone Bodies
  • Triglycerides
  • Dobutamine
  • acetoacetic acid
  • Pyruvic Acid
  • Glucose