The vascular Ca2+-sensing receptor regulates blood vessel tone and blood pressure

Am J Physiol Cell Physiol. 2016 Feb 1;310(3):C193-204. doi: 10.1152/ajpcell.00248.2015. Epub 2015 Nov 4.

Abstract

The extracellular calcium-sensing receptor CaSR is expressed in blood vessels where its role is not completely understood. In this study, we tested the hypothesis that the CaSR expressed in vascular smooth muscle cells (VSMC) is directly involved in regulation of blood pressure and blood vessel tone. Mice with targeted CaSR gene ablation from vascular smooth muscle cells (VSMC) were generated by breeding exon 7 LoxP-CaSR mice with animals in which Cre recombinase is driven by a SM22α promoter (SM22α-Cre). Wire myography performed on Cre-negative [wild-type (WT)] and Cre-positive (SM22α)CaSR(Δflox/Δflox) [knockout (KO)] mice showed an endothelium-independent reduction in aorta and mesenteric artery contractility of KO compared with WT mice in response to KCl and to phenylephrine. Increasing extracellular calcium ion (Ca(2+)) concentrations (1-5 mM) evoked contraction in WT but only relaxation in KO aortas. Accordingly, diastolic and mean arterial blood pressures of KO animals were significantly reduced compared with WT, as measured by both tail cuff and radiotelemetry. This hypotension was mostly pronounced during the animals' active phase and was not rescued by either nitric oxide-synthase inhibition with nitro-l-arginine methyl ester or by a high-salt-supplemented diet. KO animals also exhibited cardiac remodeling, bradycardia, and reduced spontaneous activity in isolated hearts and cardiomyocyte-like cells. Our findings demonstrate a role for CaSR in the cardiovascular system and suggest that physiologically relevant changes in extracellular Ca(2+) concentrations could contribute to setting blood vessel tone levels and heart rate by directly acting on the cardiovascular CaSR.

Keywords: CaSR; G protein-coupled receptor; blood pressure regulation; blood vessel tone regulation; calcium-sensing receptor; vascular smooth muscle cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Aorta / metabolism
  • Blood Pressure* / drug effects
  • Blood Pressure* / genetics
  • Bradycardia / genetics
  • Bradycardia / metabolism
  • Bradycardia / physiopathology
  • Calcium / metabolism*
  • Calcium Signaling* / drug effects
  • Calcium Signaling* / genetics
  • Dose-Response Relationship, Drug
  • Genetic Predisposition to Disease
  • Heart Rate
  • Hypotension / genetics
  • Hypotension / metabolism*
  • Hypotension / physiopathology
  • Mesenteric Arteries / metabolism
  • Mice, 129 Strain
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / metabolism*
  • Muscle, Smooth, Vascular / physiopathology
  • Myocytes, Cardiac / metabolism
  • Phenotype
  • Receptors, Calcium-Sensing
  • Receptors, G-Protein-Coupled / deficiency
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism*
  • Vasoconstriction* / drug effects
  • Vasoconstriction* / genetics
  • Vasoconstrictor Agents / pharmacology
  • Vasodilation* / drug effects
  • Vasodilation* / genetics
  • Vasodilator Agents / pharmacology
  • Ventricular Remodeling

Substances

  • CASR protein, mouse
  • Receptors, Calcium-Sensing
  • Receptors, G-Protein-Coupled
  • Vasoconstrictor Agents
  • Vasodilator Agents
  • Calcium