Effect of endothelin-3 on cytosolic calcium level in vascular endothelium and on smooth muscle contraction

Sri Agus Sudjarwo, Masatoshi Hori, Hideaki Karaki

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39 Citations (Scopus)


In isolated rat aorta, endothelin (ET)-3 increased cytosolic Ca2+ ([Ca2+]i) in the endothelium at a concentration (100 nM) which had little effect on muscle resting tone. In the absence of external Ca2+, ET-3 still transiently increased endothelial [Ca2+]i. Verapamil (10 μM) did not change the effects of ET-3. In aortas stimulated with 100 nM norepinephrine, 100 nM ET-3 relaxed the muscle with an increase in endothelial [Ca2+]i. An inhibitor of nitric oxide synthase, 100 μM NG-monomethyl-L-arginine, inhibited the relaxant effect of ET-3 but not the increase in endothelial [Ca2+]i. In the absence of the endothelium or in the presence of an antagonist of ETB receptors, 3 μM IRL 1038, the ET-3-induced increase in endothelial [Ca2+]i and relaxation of norepinephrine-induced contraction were inhibited. Under these conditions, ET-3 increased smooth muscle [Ca2+]i and induced contraction, both of which were inhibited by an inhibitor of ETA receptors, 3 μM BQ123. These results suggest that ET-3 acts on ETB receptors in the vascular endothelium to increase [Ca2+]i by releasing Ca2+ from storage sites and by opening non-L type Ca2+ channels, activates nitric oxide synthase, releases nitric oxide and relaxes vascular smooth muscle. Although ET-3 also activates ETA receptors in smooth muscle to induce contraction, this effect is overcome by the relaxant effect mediated by ETB receptors.

Original languageEnglish
Pages (from-to)137-142
Number of pages6
JournalEuropean Journal of Pharmacology
Issue number2-3
Publication statusPublished - 15 Dec 1992
Externally publishedYes


  • (Relaxation)
  • (rat aorta)
  • Ca levels (cytosolic)
  • ET receptors
  • Endothelin-3
  • Endothelium-dependent relaxation
  • Vascular


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