Mitochondrial Function and Diabetes: Consequences for Skeletal and Cardiac Muscle Metabolism

Vera B. Schrauwen-Hinderling*, Eline Kooi, Patrick Schrauwen

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

SIGNIFICANCE: An early hallmark in the development of type 2 diabetes is the resistance to the effect of insulin in skeletal muscle and in the heart. Since mitochondrial function was found to be diminished in patients with type 2 diabetes, it was suggested that this defect might be involved in the etiology of insulin resistance. Although several hypotheses were suggested, yet unclear is the mechanistic link between these two phenomena. Recent advances: Herein, we review the evidence for disturbances in mitochondrial function in skeletal muscle and the heart in the diabetic state. Also the mechanisms involved in improving mitochondrial function are considered and, whenever possible, human data is cited. Reported evidence shows that interventions that improve skeletal muscle mitochondrial function also improve insulin sensitivity in humans. In the heart, available data from animal studies suggests that enhancement of mitochondrial function can reverse aging-induced changes in heart function, and can be protective against cardiomyopathy and heart failure. FUTURE DIRECTIONS: Mitochondria and their functions can be targeted with the aim of improving skeletal muscle insulin sensitivity and cardiac function. However, human clinical intervention studies are needed to fully substantiate the potential of mitochondria as a target to prevent cardiometabolic disease.
Original languageEnglish
Pages (from-to)39-51
Number of pages13
JournalAntioxidants & Redox Signaling
Volume24
Issue number1
DOIs
Publication statusPublished - 1 Jan 2016

Keywords

  • INTRAMYOCELLULAR LIPID-CONTENT
  • FOXO TRANSCRIPTION FACTORS
  • SATURATED FATTY-ACIDS
  • PROTEIN-KINASE-C
  • CALORIE RESTRICTION
  • IN-VIVO
  • INSULIN-RESISTANCE
  • ENERGY-METABOLISM
  • PHYSICAL-ACTIVITY
  • PHOSPHOCREATINE RESYNTHESIS

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