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Endothelin-B Receptors and Left Ventricular Dysfunction after Regional versus Global Ischaemia-Reperfusion in Rat Hearts

Background. Endothelin-1 (ET-1) is implicated in left ventricular dysfunction after ischaemia-reperfusion. ETA and ETB receptors mediate diverse actions, but it is unknown whether these actions depend on ischaemia type and duration. We investigated the role of ETB receptors after four ischaemia-repe...

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Autores principales: Bibli, Sofia-Iris, Toli, Eleni V., Vilaeti, Agapi D., Varnavas, Varnavas C., Baltogiannis, Giannis G., Papalois, Apostolos, Kyriakides, Zenon S., Kolettis, Theofilos M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3403336/
https://www.ncbi.nlm.nih.gov/pubmed/22844633
http://dx.doi.org/10.1155/2012/986813
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author Bibli, Sofia-Iris
Toli, Eleni V.
Vilaeti, Agapi D.
Varnavas, Varnavas C.
Baltogiannis, Giannis G.
Papalois, Apostolos
Kyriakides, Zenon S.
Kolettis, Theofilos M.
author_facet Bibli, Sofia-Iris
Toli, Eleni V.
Vilaeti, Agapi D.
Varnavas, Varnavas C.
Baltogiannis, Giannis G.
Papalois, Apostolos
Kyriakides, Zenon S.
Kolettis, Theofilos M.
author_sort Bibli, Sofia-Iris
collection PubMed
description Background. Endothelin-1 (ET-1) is implicated in left ventricular dysfunction after ischaemia-reperfusion. ETA and ETB receptors mediate diverse actions, but it is unknown whether these actions depend on ischaemia type and duration. We investigated the role of ETB receptors after four ischaemia-reperfusion protocols in isolated rat hearts. Methods. Left ventricular haemodynamic variables were measured in the Langendorff-perfused model after 40- and 20-minute regional or global ischaemia, followed by 30-minute reperfusion. Wild-type (n = 39) and ETB-deficient (n = 41) rats were compared. Infarct size was measured using fluorescent microspheres after regional ischaemia-reperfusion. Results. Left ventricular dysfunction was more prominent in ETB-deficient rats, particularly after regional ischaemia. Infarct size was smaller (P = 0.006) in wild-type (31.5 ± 4.4%) than ETB-deficient (45.0 ± 7.3%) rats after 40 minutes of regional ischaemia-reperfusion. Although the recovery of left ventricular function was poorer after 40-minute ischaemia-reperfusion, end-diastolic pressure in ETB-deficient rats was higher after 20 than after 40 minutes of regional ischaemia-reperfusion. Conclusion. ETB receptors exert cytoprotective effects in the rat heart, mainly after regional ischaemia-reperfusion. Longer periods of ischaemia suppress the recovery of left ventricular function after reperfusion, but the role of ETB receptors may be more important during the early phases.
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spelling pubmed-34033362012-07-27 Endothelin-B Receptors and Left Ventricular Dysfunction after Regional versus Global Ischaemia-Reperfusion in Rat Hearts Bibli, Sofia-Iris Toli, Eleni V. Vilaeti, Agapi D. Varnavas, Varnavas C. Baltogiannis, Giannis G. Papalois, Apostolos Kyriakides, Zenon S. Kolettis, Theofilos M. Cardiol Res Pract Research Article Background. Endothelin-1 (ET-1) is implicated in left ventricular dysfunction after ischaemia-reperfusion. ETA and ETB receptors mediate diverse actions, but it is unknown whether these actions depend on ischaemia type and duration. We investigated the role of ETB receptors after four ischaemia-reperfusion protocols in isolated rat hearts. Methods. Left ventricular haemodynamic variables were measured in the Langendorff-perfused model after 40- and 20-minute regional or global ischaemia, followed by 30-minute reperfusion. Wild-type (n = 39) and ETB-deficient (n = 41) rats were compared. Infarct size was measured using fluorescent microspheres after regional ischaemia-reperfusion. Results. Left ventricular dysfunction was more prominent in ETB-deficient rats, particularly after regional ischaemia. Infarct size was smaller (P = 0.006) in wild-type (31.5 ± 4.4%) than ETB-deficient (45.0 ± 7.3%) rats after 40 minutes of regional ischaemia-reperfusion. Although the recovery of left ventricular function was poorer after 40-minute ischaemia-reperfusion, end-diastolic pressure in ETB-deficient rats was higher after 20 than after 40 minutes of regional ischaemia-reperfusion. Conclusion. ETB receptors exert cytoprotective effects in the rat heart, mainly after regional ischaemia-reperfusion. Longer periods of ischaemia suppress the recovery of left ventricular function after reperfusion, but the role of ETB receptors may be more important during the early phases. Hindawi Publishing Corporation 2012 2012-07-12 /pmc/articles/PMC3403336/ /pubmed/22844633 http://dx.doi.org/10.1155/2012/986813 Text en Copyright © 2012 Sofia-Iris Bibli et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bibli, Sofia-Iris
Toli, Eleni V.
Vilaeti, Agapi D.
Varnavas, Varnavas C.
Baltogiannis, Giannis G.
Papalois, Apostolos
Kyriakides, Zenon S.
Kolettis, Theofilos M.
Endothelin-B Receptors and Left Ventricular Dysfunction after Regional versus Global Ischaemia-Reperfusion in Rat Hearts
title Endothelin-B Receptors and Left Ventricular Dysfunction after Regional versus Global Ischaemia-Reperfusion in Rat Hearts
title_full Endothelin-B Receptors and Left Ventricular Dysfunction after Regional versus Global Ischaemia-Reperfusion in Rat Hearts
title_fullStr Endothelin-B Receptors and Left Ventricular Dysfunction after Regional versus Global Ischaemia-Reperfusion in Rat Hearts
title_full_unstemmed Endothelin-B Receptors and Left Ventricular Dysfunction after Regional versus Global Ischaemia-Reperfusion in Rat Hearts
title_short Endothelin-B Receptors and Left Ventricular Dysfunction after Regional versus Global Ischaemia-Reperfusion in Rat Hearts
title_sort endothelin-b receptors and left ventricular dysfunction after regional versus global ischaemia-reperfusion in rat hearts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3403336/
https://www.ncbi.nlm.nih.gov/pubmed/22844633
http://dx.doi.org/10.1155/2012/986813
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