Endothelial ETB limits vascular remodelling and development of pulmonary hypertension during hypoxia

N. F. Kelland, A. J. Bagnall, I. Morecroft, F. H. Gulliver-Sloan, Y. Dempsie, M. Nilsen, Masashi Yanagisawa, M. R. MacLean, Y. V. Kotelevtsev, D. J. Webb

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Background: We hypothesised that the potential protective effects of endothelial ETB are important in limiting pulmonary vascular muscularisation, vasoconstriction and the development of pulmonary arterial hypertension in response to hypoxia. Methods: EC-specific ETB knockout mice (EC ETB -/-) and control mice (ET B f/f) were subjected to hypobaric hypoxic (10% FiO 2) or normoxic conditions for 14 days before assessment of right ventricular pressure and pulmonary vascular morphology and function. Results: During normoxia, no difference in right ventricular pressure was detected between EC ETB -/- (23.7 ± 1.7 mm Hg) and ET B f/f mice (20.2 ± 1.5 mm Hg). Hypoxia induced an exaggerated increase in right ventricular pressure in EC ETB -/- mice (34.4 ± 1.2 mm Hg vs. 24.6 ± 1.4 mm Hg), accompanied by an increase in right ventricular mass. No effect was observed in ETB f/f mice. Endothelin-1 constricted pulmonary arteries from both groups, although maximum response was similar irrespective of inspired oxygen or genotype. Hypoxia increased the percentage of muscularised vessels in both groups of mice, but the percentage increase was significantly greater in EC ETB -/- mice. Conclusions: The potential protective effects of endothelial ETB are important in limiting pulmonary vascular muscularisation and the development of pulmonary arterial hypertension in response to hypoxia.

Original languageEnglish (US)
Pages (from-to)16-22
Number of pages7
JournalJournal of Vascular Research
Volume47
Issue number1
DOIs
StatePublished - Jan 2009

Fingerprint

Pulmonary Hypertension
Ventricular Pressure
Blood Vessels
Lung
Endothelin-1
Vasoconstriction
Knockout Mice
Pulmonary Artery
Vascular Remodeling
Hypoxia
Genotype
Oxygen

Keywords

  • Endothelin
  • ET receptor
  • Knockout
  • Pulmonary hypertension

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Kelland, N. F., Bagnall, A. J., Morecroft, I., Gulliver-Sloan, F. H., Dempsie, Y., Nilsen, M., ... Webb, D. J. (2009). Endothelial ETB limits vascular remodelling and development of pulmonary hypertension during hypoxia. Journal of Vascular Research, 47(1), 16-22. https://doi.org/10.1159/000231717

Endothelial ETB limits vascular remodelling and development of pulmonary hypertension during hypoxia. / Kelland, N. F.; Bagnall, A. J.; Morecroft, I.; Gulliver-Sloan, F. H.; Dempsie, Y.; Nilsen, M.; Yanagisawa, Masashi; MacLean, M. R.; Kotelevtsev, Y. V.; Webb, D. J.

In: Journal of Vascular Research, Vol. 47, No. 1, 01.2009, p. 16-22.

Research output: Contribution to journalArticle

Kelland, NF, Bagnall, AJ, Morecroft, I, Gulliver-Sloan, FH, Dempsie, Y, Nilsen, M, Yanagisawa, M, MacLean, MR, Kotelevtsev, YV & Webb, DJ 2009, 'Endothelial ETB limits vascular remodelling and development of pulmonary hypertension during hypoxia', Journal of Vascular Research, vol. 47, no. 1, pp. 16-22. https://doi.org/10.1159/000231717
Kelland NF, Bagnall AJ, Morecroft I, Gulliver-Sloan FH, Dempsie Y, Nilsen M et al. Endothelial ETB limits vascular remodelling and development of pulmonary hypertension during hypoxia. Journal of Vascular Research. 2009 Jan;47(1):16-22. https://doi.org/10.1159/000231717
Kelland, N. F. ; Bagnall, A. J. ; Morecroft, I. ; Gulliver-Sloan, F. H. ; Dempsie, Y. ; Nilsen, M. ; Yanagisawa, Masashi ; MacLean, M. R. ; Kotelevtsev, Y. V. ; Webb, D. J. / Endothelial ETB limits vascular remodelling and development of pulmonary hypertension during hypoxia. In: Journal of Vascular Research. 2009 ; Vol. 47, No. 1. pp. 16-22.
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abstract = "Background: We hypothesised that the potential protective effects of endothelial ETB are important in limiting pulmonary vascular muscularisation, vasoconstriction and the development of pulmonary arterial hypertension in response to hypoxia. Methods: EC-specific ETB knockout mice (EC ETB -/-) and control mice (ET B f/f) were subjected to hypobaric hypoxic (10{\%} FiO 2) or normoxic conditions for 14 days before assessment of right ventricular pressure and pulmonary vascular morphology and function. Results: During normoxia, no difference in right ventricular pressure was detected between EC ETB -/- (23.7 ± 1.7 mm Hg) and ET B f/f mice (20.2 ± 1.5 mm Hg). Hypoxia induced an exaggerated increase in right ventricular pressure in EC ETB -/- mice (34.4 ± 1.2 mm Hg vs. 24.6 ± 1.4 mm Hg), accompanied by an increase in right ventricular mass. No effect was observed in ETB f/f mice. Endothelin-1 constricted pulmonary arteries from both groups, although maximum response was similar irrespective of inspired oxygen or genotype. Hypoxia increased the percentage of muscularised vessels in both groups of mice, but the percentage increase was significantly greater in EC ETB -/- mice. Conclusions: The potential protective effects of endothelial ETB are important in limiting pulmonary vascular muscularisation and the development of pulmonary arterial hypertension in response to hypoxia.",
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AU - Dempsie, Y.

AU - Nilsen, M.

AU - Yanagisawa, Masashi

AU - MacLean, M. R.

AU - Kotelevtsev, Y. V.

AU - Webb, D. J.

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