Abstract

Despite epidemiological evidence showing that diets rich in whole grains reduce the risk of chronic life-style related diseases, biological mechanisms for these positive effects are mostly unknown. Increased 5-aminovaleric acid betaine (5-AVAB) levels in plasma and metabolically active tissues such as heart have been associated with consumption of diets rich in whole grains. However, biological effects of 5-AVAB are poorly understood. We evaluated 5-AVAB concentrations in human and mouse heart tissue (3–22 µM and 38–78 µM, respectively) using mass spectrometry. We show that 5-AVAB, at physiological concentration range, dose-dependently inhibits oxygen consumption due to β-oxidation of fatty acids, but does not otherwise compromise mitochondrial respiration, as measured with oxygen consumption rate in cultured mouse primary cardiomyocytes. We also demonstrate that this effect is caused by 5-AVAB induced reduction of cellular L-carnitine. Reduced L-carnitine levels are at least partly mediated by the inhibition of cell membrane carnitine transporter (OCTN2) as evaluated by in silico docking, and by siRNA mediated silencing of OCTN2 in cultured cardiomyocytes. 5-AVAB caused inhibition of β-oxidation of fatty acids is a novel mechanism on how diets rich in whole grains may regulate energy metabolism in the body. Elucidating potentially beneficial effects of 5-AVAB e.g. on cardiac physiology will require further in vivo investigations.

Highlights

  • Epidemiological evidence shows that diets rich in whole grains reduce the risk of chronic life-style related diseases, including cardiovascular disorders[1,2,3,4]

  • In order to define physiological concentrations of 5-aminovaleric acid betaine (5-AVAB), we examined human and mouse heart tissue with the targeted mass spectrometry method

  • We noticed that when cells exposed to 5-AVAB for 24 h were supplemented with medium containing palmitate as a sole energy source prior to the Seahorse assay, the oxygen consumption rate (OCR) decreased during the assay, whereas in vehicle treated cells OCR remained constant (Fig. 1)

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Summary

Introduction

Epidemiological evidence shows that diets rich in whole grains reduce the risk of chronic life-style related diseases, including cardiovascular disorders[1,2,3,4]. 5-AVAB has similar molecular structure with meldonium (mildronate), a drug that inhibits β-oxidation of fatty acids and has been associated with improved cardiac mitochondrial function after ischemia[6]. Our hypothesis was that 5-AVAB, like meldonium, reduces β-oxidation of fatty acid by blocking OCTN2.

Results
Conclusion

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