Increased activation of stromal interaction molecule-1/Orai-1 in aorta from hypertensive rats: a novel insight into vascular dysfunction

Hypertension. 2009 Feb;53(2):409-16. doi: 10.1161/HYPERTENSIONAHA.108.124404. Epub 2008 Dec 15.

Abstract

Disturbances in the regulation of cytosolic calcium (Ca(2+)) concentration play a key role in the vascular dysfunction associated with arterial hypertension. Stromal interaction molecules (STIMs) and Orai proteins represent a novel mechanism to control store-operated Ca(2+) entry. Although STIMs act as Ca(2+) sensors for the intracellular Ca(2+) stores, Orai is the putative pore-forming component of Ca(2+) release-activated Ca(2+) channels at the plasma membrane. We hypothesized that augmented activation of Ca(2+) release-activated Ca(2+)/Orai-1, through enhanced activity of STIM-1, plays a role in increased basal tonus and vascular reactivity in hypertensive animals. Endothelium-denuded aortic rings from Wistar-Kyoto and stroke-prone spontaneously hypertensive rats were used to evaluate contractions because of Ca(2+) influx. Depletion of intracellular Ca(2+) stores, which induces Ca(2+) release-activated Ca(2+) activation, was performed by placing arteries in Ca(2+) free-EGTA buffer. The addition of the Ca(2+) regular buffer produced greater contractions in aortas from stroke-prone spontaneously hypertensive rats versus Wistar-Kyoto rats. Thapsigargin (10 micromol/L), an inhibitor of the sarcoplasmic reticulum Ca(2+) ATPase, further increased these contractions, especially in stroke-prone spontaneously hypertensive rat aorta. Addition of the Ca(2+) release-activated Ca(2+) channel inhibitors 2-aminoethoxydiphenyl borate (100 micromol/L) or gadolinium (100 micromol/L), as well as neutralizing antibodies to STIM-1 or Orai-1, abolished thapsigargin-increased contraction and the differences in spontaneous tone between the groups. Expression of Orai-1 and STIM-1 proteins was increased in aorta from stroke-prone spontaneously hypertensive rats when compared with Wistar-Kyoto rats. These results support the hypothesis that both Orai-1 and STIM-1 contribute to abnormal vascular function in hypertension. Augmented activation of STIM-1/Orai-1 may represent the mechanism that leads to impaired control of intracellular Ca(2+) levels in hypertension.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aorta / drug effects
  • Aorta / metabolism*
  • Aorta / physiopathology
  • Blood Pressure / physiology
  • Body Weight / physiology
  • Calcium / metabolism*
  • Calcium Channels / metabolism*
  • Cytosol / metabolism
  • Disease Models, Animal
  • Enzyme Inhibitors / pharmacology
  • Homeostasis / physiology
  • Hypertension / metabolism*
  • Male
  • Membrane Glycoproteins / metabolism*
  • Muscle Contraction / drug effects
  • ORAI1 Protein
  • Rats
  • Rats, Inbred SHR
  • Rats, Inbred WKY
  • Stromal Interaction Molecule 1
  • Thapsigargin / pharmacology

Substances

  • Calcium Channels
  • Enzyme Inhibitors
  • Membrane Glycoproteins
  • ORAI1 Protein
  • Orai1 protein, rat
  • Stim1 protein, rat
  • Stromal Interaction Molecule 1
  • Thapsigargin
  • Calcium