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The Effect of Antivascular Endothelial Growth Factor on the Development of Adhesion Formation in Laparotomized Rats: Experimental Study

Aims. This study determined the effects of a single dose of bevacizumab, an antiangiogenic recombinant monoclonal antibody that specifically targets vascular endothelial growth factor (VEGF), on adhesion formation in the rat cecal abrasion model. Methodology. Thirty female Wistar albino rats (200–22...

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Autores principales: Basbug, Murat, Bulbuller, Nurullah, Camci, Cemalettin, Ayten, Refik, Aygen, Erhan, Ozercan, Ibrahim Hanifi, Arikanoglu, Zulfu, Akbulut, Sami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3132490/
https://www.ncbi.nlm.nih.gov/pubmed/21760775
http://dx.doi.org/10.1155/2011/578691
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author Basbug, Murat
Bulbuller, Nurullah
Camci, Cemalettin
Ayten, Refik
Aygen, Erhan
Ozercan, Ibrahim Hanifi
Arikanoglu, Zulfu
Akbulut, Sami
author_facet Basbug, Murat
Bulbuller, Nurullah
Camci, Cemalettin
Ayten, Refik
Aygen, Erhan
Ozercan, Ibrahim Hanifi
Arikanoglu, Zulfu
Akbulut, Sami
author_sort Basbug, Murat
collection PubMed
description Aims. This study determined the effects of a single dose of bevacizumab, an antiangiogenic recombinant monoclonal antibody that specifically targets vascular endothelial growth factor (VEGF), on adhesion formation in the rat cecal abrasion model. Methodology. Thirty female Wistar albino rats (200–224 g) were divided into three groups. All rats underwent laparotomy at which time cecal wall abrasion and abdominal wall injuries were induced. Group I (control) underwent only the abrasion procedure; Groups II and III received saline or bevacizumab intraperitoneally, respectively, following the abrasion. The rats were killed on postoperative day 7, and the severity of adhesions was evaluated, together with histopathological fibrosis parameters and immunohistochemical staining to identify the VEGF receptor. Results. The mean adhesion severity score in Groups I–III was 2.5 ± 0.52, 2.4 ± 0.69, and 0.7 ± 0.82, respectively; the score in Group III was significantly lower than that in Groups I (P < 0.001) and II (P < 0.001). In the histopathological evaluation, the mean fibrosis score in Group III was significantly lower that the scores in Groups I (P < 0.001) and II (P < 0.001). VEGF staining of the adhesion areas in Group III was significantly lower than that in Groups I (P < 0.001) and II (P < 0.001). Conclusion. Bevacizumab decreases adhesion formation following laparotomy in rats by blocking VEGF receptor occupancy.
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spelling pubmed-31324902011-07-14 The Effect of Antivascular Endothelial Growth Factor on the Development of Adhesion Formation in Laparotomized Rats: Experimental Study Basbug, Murat Bulbuller, Nurullah Camci, Cemalettin Ayten, Refik Aygen, Erhan Ozercan, Ibrahim Hanifi Arikanoglu, Zulfu Akbulut, Sami Gastroenterol Res Pract Research Article Aims. This study determined the effects of a single dose of bevacizumab, an antiangiogenic recombinant monoclonal antibody that specifically targets vascular endothelial growth factor (VEGF), on adhesion formation in the rat cecal abrasion model. Methodology. Thirty female Wistar albino rats (200–224 g) were divided into three groups. All rats underwent laparotomy at which time cecal wall abrasion and abdominal wall injuries were induced. Group I (control) underwent only the abrasion procedure; Groups II and III received saline or bevacizumab intraperitoneally, respectively, following the abrasion. The rats were killed on postoperative day 7, and the severity of adhesions was evaluated, together with histopathological fibrosis parameters and immunohistochemical staining to identify the VEGF receptor. Results. The mean adhesion severity score in Groups I–III was 2.5 ± 0.52, 2.4 ± 0.69, and 0.7 ± 0.82, respectively; the score in Group III was significantly lower than that in Groups I (P < 0.001) and II (P < 0.001). In the histopathological evaluation, the mean fibrosis score in Group III was significantly lower that the scores in Groups I (P < 0.001) and II (P < 0.001). VEGF staining of the adhesion areas in Group III was significantly lower than that in Groups I (P < 0.001) and II (P < 0.001). Conclusion. Bevacizumab decreases adhesion formation following laparotomy in rats by blocking VEGF receptor occupancy. Hindawi Publishing Corporation 2011 2011-06-28 /pmc/articles/PMC3132490/ /pubmed/21760775 http://dx.doi.org/10.1155/2011/578691 Text en Copyright © 2011 Murat Basbug 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
Basbug, Murat
Bulbuller, Nurullah
Camci, Cemalettin
Ayten, Refik
Aygen, Erhan
Ozercan, Ibrahim Hanifi
Arikanoglu, Zulfu
Akbulut, Sami
The Effect of Antivascular Endothelial Growth Factor on the Development of Adhesion Formation in Laparotomized Rats: Experimental Study
title The Effect of Antivascular Endothelial Growth Factor on the Development of Adhesion Formation in Laparotomized Rats: Experimental Study
title_full The Effect of Antivascular Endothelial Growth Factor on the Development of Adhesion Formation in Laparotomized Rats: Experimental Study
title_fullStr The Effect of Antivascular Endothelial Growth Factor on the Development of Adhesion Formation in Laparotomized Rats: Experimental Study
title_full_unstemmed The Effect of Antivascular Endothelial Growth Factor on the Development of Adhesion Formation in Laparotomized Rats: Experimental Study
title_short The Effect of Antivascular Endothelial Growth Factor on the Development of Adhesion Formation in Laparotomized Rats: Experimental Study
title_sort effect of antivascular endothelial growth factor on the development of adhesion formation in laparotomized rats: experimental study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3132490/
https://www.ncbi.nlm.nih.gov/pubmed/21760775
http://dx.doi.org/10.1155/2011/578691
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