Vasorelaxant Effect of 5'-Methylthioadenosine Obtained from Candida utilis Yeast Extract through the Suppression of Intracellular Ca(2+) Concentration in Isolated Rat Aorta

J Agric Food Chem. 2016 May 4;64(17):3362-70. doi: 10.1021/acs.jafc.6b00679. Epub 2016 Apr 20.

Abstract

Our study is the first to demonstrate the vasorelaxant effect of Candida utilis yeast extract on rat aorta (EC50 of 7.2 ± 3.2 mg/mL). Among five identified compounds, 5'-methylthioadenosine (MTA) exhibited comparable vasorelaxant effect (EC50 of 190 ± 40 μM) with adenosine, a known vasodilator, on 1 μM phenylephrine (PE)-contracted Sprague-Dawley rat aortic rings. MTA induced vasorelaxation in an endothelium-independent manner and independent of the adenosine receptors. MTA reduced a CaCl2-induced vasocontraction stimulated by 1 μM PE, whereas the effect was abolished in a 60 mM KCl-induced vasocontraction. This indicates that MTA was not involved in the suppression of extracellular Ca(2+) influx. MTA significantly (P < 0.01) attenuated the PE-induced activation of calmodulin-dependent kinase II (CaMK II) in aortic rings and inhibited the phosphorylation of L-type Ca(2+) channel (VDCC). In conclusion, the underlying mechanism(s) of MTA-induced vasorelaxation involves the inhibition of Ca(2+)/CaMK II/VDCC phosphorylation pathway, resulting in the suppression of intracellular Ca(2+) concentration in aortic rings.

Keywords: 5′-methylthioadenosine; Ca2+ channel; calmodulin-dependent kinase II; vasorelaxation; yeast extract.

MeSH terms

  • Animals
  • Aorta / drug effects*
  • Aorta / metabolism
  • Calcium / metabolism*
  • Candida / chemistry*
  • Chromatography, High Pressure Liquid
  • Deoxyadenosines / pharmacology*
  • In Vitro Techniques
  • Male
  • Mass Spectrometry
  • Rats
  • Rats, Sprague-Dawley
  • Thionucleosides / pharmacology*
  • Vasodilator Agents / pharmacology*

Substances

  • Deoxyadenosines
  • Thionucleosides
  • Vasodilator Agents
  • 5'-methylthioadenosine
  • Calcium