Lysophosphatidic acid causes endothelial dysfunction in porcine coronary arteries and human coronary artery endothelial cells

Atherosclerosis. 2012 May;222(1):74-83. doi: 10.1016/j.atherosclerosis.2012.02.010. Epub 2012 Feb 13.

Abstract

Aim: The objective of this study was to determine the effects of lysophosphatidic acid (LPA) on endothelial functions and molecular alternations in both porcine coronary arteries and human coronary artery endothelial cells (HCAECs).

Methods and results: The vessel rings and HCAECs were treated with clinically relevant concentrations of LPA for different times. Vasomotor reactivity was studied with a myograph tension system. LPA (10 and 50 μM) treatment for the vessel rings significantly reduced endothelium-dependent vasorelaxation in response to bradykinin (×10(-5)M) by 32% and 49%, respectively, compared with the control (P<0.05). LPA decreased endothelial nitric oxide synthase (eNOS) mRNA and immunoreactivity levels in the vessel rings. In HCAECs, LPA reduced eNOS mRNA, phospho-eNOS and total eNOS protein levels. In addition, superoxide anion levels in LPA-treated vessel rings and HCAECs were significantly increased by lucegenin-enhanced chemiluminescence assay and dihydroethidium staining, respectively. Mitochondrial membrane potential and ATP content in LPA-treated HCAECs were substantially decreased. The mRNA levels of reactive oxygen species generating enzymes NOX4 and p40(phox) were increased, while endogenous antioxidant enzyme superoxide dismutase 1 was decreased in response to LPA treatment in HCAECs. Furthermore, exogenous antioxidant molecule selenomethionine (SeMet) effectively reversed these LPA-induced effects in both porcine coronary arteries and HCAECs.

Conclusions: LPA causes endothelial dysfunction by a mechanism associated with decreased eNOS expression and increased oxidative stress in porcine coronary arteries and HCAECs.

Publication types

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

MeSH terms

  • Animals
  • Atherosclerosis / physiopathology*
  • Bradykinin / pharmacology
  • Coronary Vessels / drug effects*
  • Down-Regulation
  • Endothelium, Vascular / drug effects
  • Humans
  • Lysophospholipids / pharmacology*
  • Membrane Potential, Mitochondrial / drug effects
  • Nitric Oxide Synthase Type III / biosynthesis
  • Oxidative Stress / drug effects
  • Selenomethionine / pharmacology
  • Superoxide Dismutase / metabolism
  • Superoxide Dismutase-1
  • Superoxides / metabolism
  • Swine
  • Vasodilation / drug effects*

Substances

  • Lysophospholipids
  • SOD1 protein, human
  • Superoxides
  • Selenomethionine
  • Nitric Oxide Synthase Type III
  • Superoxide Dismutase
  • Superoxide Dismutase-1
  • lysophosphatidic acid
  • Bradykinin