Maternal high salt diet altered Adenosine-mediated vasodilatation via PKA/BK channel pathway in offspring rats

Mol Nutr Food Res. 2017 Aug;61(8). doi: 10.1002/mnfr.201600963. Epub 2017 Mar 3.

Abstract

Scope: High salt (HS) diets are related to cardiovascular diseases, and prenatal HS was suggested to increase risks of coronary artery diseases in the offspring. This study tested the hypothesis that prenatal HS may influence Adenosine-induced vasodilatation via protein kinase A (PKA) pathway in coronary arteries.

Methods and results: Sprague-Dawley rats were fed with 8% salt diet for gestation, the control was fed with 0.3% salt diet. Coronary arteries from male adult offspring were tested for K+ channels and Adenosine signal pathways. Adenosine-mediated vasodilatation was reduced in coronary arteries in HS. There was no difference in gene expression of A2A receptors between the two groups. After pretreatment with PKA inhibitor, vasodilatation to Adenosine was decreased to a smaller extent in HS than that in control. Forskolin (activator of adenylate cyclase)-mediated vasodilatation was decreased in HS. Iberiotoxin (large-conductance Ca2+ -activated K+ channel [BK channel] inhibitor) attenuated Forskolin-induced vasodilatation in control, not in HS group. Currents of BK channels decreased in coronary artery smooth muscle cells, and PKA-modulated BK channel functions were declined. Protein levels of BK β1 and PKA C-subunits in coronary arteries of HS offspring were reduced.

Conclusions: Prenatal HS diets altered Adenosine-mediated coronary artery vasodilatation in the offspring, which was linked to downregulation of cAMP/PKA/BK channel pathway.

Keywords: Adenosine; Coronary arteries; Large-conductance Ca2+-activated K+ channel; Prenatal high salt; Vasodilatation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine / metabolism*
  • Adenosine / pharmacology
  • Animals
  • Animals, Newborn
  • Coronary Vessels / drug effects*
  • Coronary Vessels / metabolism
  • Cyclic AMP / metabolism
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Female
  • Large-Conductance Calcium-Activated Potassium Channels / metabolism
  • Male
  • Maternal Nutritional Physiological Phenomena
  • Muscle, Smooth, Vascular / cytology
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / metabolism
  • Pregnancy
  • Prenatal Exposure Delayed Effects
  • Rats, Sprague-Dawley
  • Receptor, Adenosine A2A / metabolism
  • Signal Transduction
  • Sodium Chloride, Dietary / pharmacology*
  • Vasodilation / drug effects*

Substances

  • Large-Conductance Calcium-Activated Potassium Channels
  • Receptor, Adenosine A2A
  • Sodium Chloride, Dietary
  • Cyclic AMP
  • Cyclic AMP-Dependent Protein Kinases
  • Adenosine