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Effect of 1α-25-dihydroxyvitamin D(3) on intimal hyperplasia developing in vascular anastomoses: a rabbit model

INTRODUCTION: A common problem encountered in routine daily practice of cardiovascular surgery is migration of smooth muscle cells leading to intimal hyperplasia developing at vascular anastomosis sites which then causes luminal narrowing. The aim of this study was to investigate the antiproliferati...

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Autores principales: Yurekli, Ismail, Gokalp, Orhan, Kiray, Muge, Bademci, Mehmet, Yetkin, Ufuk, Ergunes, Kazim, Yilmaz, Osman, Bayrak, Serdar, Gurbuz, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701962/
https://www.ncbi.nlm.nih.gov/pubmed/23847659
http://dx.doi.org/10.5114/aoms.2012.30786
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author Yurekli, Ismail
Gokalp, Orhan
Kiray, Muge
Bademci, Mehmet
Yetkin, Ufuk
Ergunes, Kazim
Yilmaz, Osman
Bayrak, Serdar
Gurbuz, Ali
author_facet Yurekli, Ismail
Gokalp, Orhan
Kiray, Muge
Bademci, Mehmet
Yetkin, Ufuk
Ergunes, Kazim
Yilmaz, Osman
Bayrak, Serdar
Gurbuz, Ali
author_sort Yurekli, Ismail
collection PubMed
description INTRODUCTION: A common problem encountered in routine daily practice of cardiovascular surgery is migration of smooth muscle cells leading to intimal hyperplasia developing at vascular anastomosis sites which then causes luminal narrowing. The aim of this study was to investigate the antiproliferative effect of 1,25 (OH)(2)D(3) on intimal hyperplasia. MATERIAL AND METHODS: Twenty-one male white New Zealand rabbits weighing 2-3 kg were selected. There were 3 groups of animals each consisting of 7 rabbits. Group 1 was the control group. Group 2 was the sham group and group 3 consisted of rabbits receiving 1,25 (OH)(2)D(3). The right carotid arteries of the subjects in groups 2 and 3 were transected and re-anastomosed. A daily dose of 25 ng 1,25 (OH)(2)D(3) per 100 g body weight was administered for 14 days to rabbits in group 3. Rabbits in group 2 were not subject to any pharmaceutical agent. All the subjects were sacrificed at the end of the 28(th) postoperative day. Their right carotid arteries were resected and then investigated histopathologically. RESULTS: Intimal thickness and intimal area were measured as significantly lower in group 1 when compared with the other groups (p = 0.004). In group 3, the ratios of thickness of tunica intima/thickness of tunica media and area of tunica intima/area of tunica media were significantly lower than those of group 2 (p = 0.015, p = 0.003). CONCLUSIONS: 1,25 (OH)(2)D(3), the active metabolite of vitamin D, reduces the intimal hyperplasia developing after vascular anastomoses.
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spelling pubmed-37019622013-07-11 Effect of 1α-25-dihydroxyvitamin D(3) on intimal hyperplasia developing in vascular anastomoses: a rabbit model Yurekli, Ismail Gokalp, Orhan Kiray, Muge Bademci, Mehmet Yetkin, Ufuk Ergunes, Kazim Yilmaz, Osman Bayrak, Serdar Gurbuz, Ali Arch Med Sci Experimental Research INTRODUCTION: A common problem encountered in routine daily practice of cardiovascular surgery is migration of smooth muscle cells leading to intimal hyperplasia developing at vascular anastomosis sites which then causes luminal narrowing. The aim of this study was to investigate the antiproliferative effect of 1,25 (OH)(2)D(3) on intimal hyperplasia. MATERIAL AND METHODS: Twenty-one male white New Zealand rabbits weighing 2-3 kg were selected. There were 3 groups of animals each consisting of 7 rabbits. Group 1 was the control group. Group 2 was the sham group and group 3 consisted of rabbits receiving 1,25 (OH)(2)D(3). The right carotid arteries of the subjects in groups 2 and 3 were transected and re-anastomosed. A daily dose of 25 ng 1,25 (OH)(2)D(3) per 100 g body weight was administered for 14 days to rabbits in group 3. Rabbits in group 2 were not subject to any pharmaceutical agent. All the subjects were sacrificed at the end of the 28(th) postoperative day. Their right carotid arteries were resected and then investigated histopathologically. RESULTS: Intimal thickness and intimal area were measured as significantly lower in group 1 when compared with the other groups (p = 0.004). In group 3, the ratios of thickness of tunica intima/thickness of tunica media and area of tunica intima/area of tunica media were significantly lower than those of group 2 (p = 0.015, p = 0.003). CONCLUSIONS: 1,25 (OH)(2)D(3), the active metabolite of vitamin D, reduces the intimal hyperplasia developing after vascular anastomoses. Termedia Publishing House 2012-10-08 2013-06-20 /pmc/articles/PMC3701962/ /pubmed/23847659 http://dx.doi.org/10.5114/aoms.2012.30786 Text en Copyright © 2013 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
Yurekli, Ismail
Gokalp, Orhan
Kiray, Muge
Bademci, Mehmet
Yetkin, Ufuk
Ergunes, Kazim
Yilmaz, Osman
Bayrak, Serdar
Gurbuz, Ali
Effect of 1α-25-dihydroxyvitamin D(3) on intimal hyperplasia developing in vascular anastomoses: a rabbit model
title Effect of 1α-25-dihydroxyvitamin D(3) on intimal hyperplasia developing in vascular anastomoses: a rabbit model
title_full Effect of 1α-25-dihydroxyvitamin D(3) on intimal hyperplasia developing in vascular anastomoses: a rabbit model
title_fullStr Effect of 1α-25-dihydroxyvitamin D(3) on intimal hyperplasia developing in vascular anastomoses: a rabbit model
title_full_unstemmed Effect of 1α-25-dihydroxyvitamin D(3) on intimal hyperplasia developing in vascular anastomoses: a rabbit model
title_short Effect of 1α-25-dihydroxyvitamin D(3) on intimal hyperplasia developing in vascular anastomoses: a rabbit model
title_sort effect of 1α-25-dihydroxyvitamin d(3) on intimal hyperplasia developing in vascular anastomoses: a rabbit model
topic Experimental Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701962/
https://www.ncbi.nlm.nih.gov/pubmed/23847659
http://dx.doi.org/10.5114/aoms.2012.30786
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