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Vasoconstrictive effects of levobupivacaine on the basilar artery in the rabbit

INTRODUCTION: Spinal anesthesia is a widely used technique of the modern practice of anesthesia. Spinal cord ischemia is a rare but catastrophic complication of spinal anesthesia which may be caused by a direct vasoconstrictive effect of the local anesthetic. Although the vasoconstrictive effects of...

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Autores principales: Ergil, Julide, Kertmen, Hayri, Sayın, Murat, Gürer, Bora, Yılmaz, Erdal Reşit, Özkan, Derya, Arıkök, Ata Türker, Kanat, Mehmet Ali, Şekerci, Zeki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495161/
https://www.ncbi.nlm.nih.gov/pubmed/26170861
http://dx.doi.org/10.5114/aoms.2015.52372
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author Ergil, Julide
Kertmen, Hayri
Sayın, Murat
Gürer, Bora
Yılmaz, Erdal Reşit
Özkan, Derya
Arıkök, Ata Türker
Kanat, Mehmet Ali
Şekerci, Zeki
author_facet Ergil, Julide
Kertmen, Hayri
Sayın, Murat
Gürer, Bora
Yılmaz, Erdal Reşit
Özkan, Derya
Arıkök, Ata Türker
Kanat, Mehmet Ali
Şekerci, Zeki
author_sort Ergil, Julide
collection PubMed
description INTRODUCTION: Spinal anesthesia is a widely used technique of the modern practice of anesthesia. Spinal cord ischemia is a rare but catastrophic complication of spinal anesthesia which may be caused by a direct vasoconstrictive effect of the local anesthetic. Although the vasoconstrictive effects of levobupivacaine have been widely studied, the vasoconstrictive effects of this drug on the intradural arteries have never been studied. The aim of this study is to evaluate whether levobupivacaine has vasoconstrictive effects on the basilar artery in rabbits. MATERIAL AND METHODS: Thirty male New Zealand white rabbits were divided randomly into three groups of ten rabbits each: group 1 (control); group 2 (0.125% levobupivacaine); group 3 (0.25% levobupivacaine). The cisterna magna was punctured as described below, then 1 ml of saline or 0.125% or 0.25% levobupivacaine was injected into the cisterna magna in 10 min by an infusion pump in groups 1, 2 and 3 respectively. All animals were euthanized by perfusion-fixation 30 min after the procedure. The luminal area and the size of the cross-sectional area for each basilar artery were measured. RESULTS: Both 0.125% and 0.25% levobupivacaine infusion caused significant vasoconstriction. Vasoconstriction was more significant for the 0.125% concentration. CONCLUSIONS: The results of this study indicated that both 0.125% and 0.25% concentrations of levobupivacaine caused significant vasoconstriction of the basilar artery when administered into the subarachnoid space. This may constitute proof that subarachnoid administration of levobupivacaine may diminish the spinal cord blood flow, causing ischemia.
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spelling pubmed-44951612015-07-13 Vasoconstrictive effects of levobupivacaine on the basilar artery in the rabbit Ergil, Julide Kertmen, Hayri Sayın, Murat Gürer, Bora Yılmaz, Erdal Reşit Özkan, Derya Arıkök, Ata Türker Kanat, Mehmet Ali Şekerci, Zeki Arch Med Sci Experimental Research INTRODUCTION: Spinal anesthesia is a widely used technique of the modern practice of anesthesia. Spinal cord ischemia is a rare but catastrophic complication of spinal anesthesia which may be caused by a direct vasoconstrictive effect of the local anesthetic. Although the vasoconstrictive effects of levobupivacaine have been widely studied, the vasoconstrictive effects of this drug on the intradural arteries have never been studied. The aim of this study is to evaluate whether levobupivacaine has vasoconstrictive effects on the basilar artery in rabbits. MATERIAL AND METHODS: Thirty male New Zealand white rabbits were divided randomly into three groups of ten rabbits each: group 1 (control); group 2 (0.125% levobupivacaine); group 3 (0.25% levobupivacaine). The cisterna magna was punctured as described below, then 1 ml of saline or 0.125% or 0.25% levobupivacaine was injected into the cisterna magna in 10 min by an infusion pump in groups 1, 2 and 3 respectively. All animals were euthanized by perfusion-fixation 30 min after the procedure. The luminal area and the size of the cross-sectional area for each basilar artery were measured. RESULTS: Both 0.125% and 0.25% levobupivacaine infusion caused significant vasoconstriction. Vasoconstriction was more significant for the 0.125% concentration. CONCLUSIONS: The results of this study indicated that both 0.125% and 0.25% concentrations of levobupivacaine caused significant vasoconstriction of the basilar artery when administered into the subarachnoid space. This may constitute proof that subarachnoid administration of levobupivacaine may diminish the spinal cord blood flow, causing ischemia. Termedia Publishing House 2015-06-19 2015-06-19 /pmc/articles/PMC4495161/ /pubmed/26170861 http://dx.doi.org/10.5114/aoms.2015.52372 Text en Copyright © 2015 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Experimental Research
Ergil, Julide
Kertmen, Hayri
Sayın, Murat
Gürer, Bora
Yılmaz, Erdal Reşit
Özkan, Derya
Arıkök, Ata Türker
Kanat, Mehmet Ali
Şekerci, Zeki
Vasoconstrictive effects of levobupivacaine on the basilar artery in the rabbit
title Vasoconstrictive effects of levobupivacaine on the basilar artery in the rabbit
title_full Vasoconstrictive effects of levobupivacaine on the basilar artery in the rabbit
title_fullStr Vasoconstrictive effects of levobupivacaine on the basilar artery in the rabbit
title_full_unstemmed Vasoconstrictive effects of levobupivacaine on the basilar artery in the rabbit
title_short Vasoconstrictive effects of levobupivacaine on the basilar artery in the rabbit
title_sort vasoconstrictive effects of levobupivacaine on the basilar artery in the rabbit
topic Experimental Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495161/
https://www.ncbi.nlm.nih.gov/pubmed/26170861
http://dx.doi.org/10.5114/aoms.2015.52372
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