Mitochondrial Fission Inhibitors Suppress Endothelin-1-Induced Artery Constriction

Cell Physiol Biochem. 2017;42(5):1802-1811. doi: 10.1159/000479536. Epub 2017 Jul 27.

Abstract

Background/aims: Endothelin-1 is implicated in the pathogenesis of hypertension, but the underlying mechanisms remained elusive. Our previous study found that inhibition of mitochondrial fission of smooth muscle cells suppressed phenylephrine- and high K+-induced artery constriction. Here, we studied the effects of mitochondrial fission inhibitors on endothelin-1-induced vasoconstriction.

Methods: The tension of rat mesenteric arteries and thoracic aorta was measured by using a multi-wire myograph system. Mitochondrial morphology of aortic smooth muscle cells was observed by using transmission electron microscopy.

Results: Dynamin-related protein-1 selective inhibitor mdivi-1 relaxed endothelin-1-induced constriction, and mdivi-1 pre-treatment prevented endothelin-1-induced constriction of rat mesenteric arteries with intact and denuded endothelium. Mdivi-1 had a similar inhibitory effect on rat thoracic aorta. Another mitochondrial fission inhibitor dynasore showed similar effects as mdivi-1 in rat mesenteric arteries. Mdivi-1 inhibited endothelin-1-induced increase of mitochondrial fission in smooth muscle cells of rat aorta. Rho-associated protein kinase inhibitor Y-27632 which relaxed endothelin-1-induced vasoconstriction inhibited endothelin-1-induced mitochondrial fission in smooth muscle cells of rat aorta.

Conclusion: Endothelin-1 increases mitochondrial fission in vascular smooth muscle cells, and mitochondrial fission inhibitors suppress endothelin-1-induced vasoconstriction.

Keywords: Endothelin-1; Mdivi-1; Mitochondrial fission; Vascular smooth muscle.

MeSH terms

  • Amides / pharmacology
  • Animals
  • Aorta, Thoracic / cytology
  • Aorta, Thoracic / drug effects
  • Aorta, Thoracic / physiology*
  • Dynamins / antagonists & inhibitors
  • Dynamins / metabolism
  • Endothelin-1 / antagonists & inhibitors
  • Endothelin-1 / metabolism*
  • Hydrazones / pharmacology
  • Male
  • Mesenteric Arteries / drug effects
  • Mesenteric Arteries / physiology*
  • Microscopy, Electron, Transmission
  • Mitochondria / pathology
  • Mitochondrial Dynamics / drug effects*
  • Myocytes, Smooth Muscle / drug effects
  • Myocytes, Smooth Muscle / metabolism
  • Pyridines / pharmacology
  • Quinazolinones / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species / metabolism
  • Vasoconstriction / drug effects

Substances

  • 3-(2,4-dichloro-5-methoxyphenyl)-2-sulfanyl-4(3H)-quinazolinone
  • Amides
  • Endothelin-1
  • Hydrazones
  • N'-(3,4-dihydroxybenzylidene)-3-hydroxy-2-naphthahydrazide
  • Pyridines
  • Quinazolinones
  • Reactive Oxygen Species
  • Y 27632
  • Dnm1l protein, rat
  • Dynamins