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Effects of sildenafil and tadalafil on skin flap viability
Vascular complication is one of the causes of skin flap healing failure. Sildenafil and tadalafil, a type-5 phosphodiesterase inhibitor, can improve flap viability, however, the action mechanisms involved in this process are still unclear. To assess the effects of orally administered sildenafil and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850220/ https://www.ncbi.nlm.nih.gov/pubmed/33715076 http://dx.doi.org/10.1007/s00403-021-02196-0 |
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author | Souza, Rafael A. C. Martinelli-Kläy, Carla Patrícia d’Acampora, Armando J. Bernardes, Geraldo J. S. Sgrott, Sandro M. Souza, Laila A. C. Lombardi, Tommaso Sudbrack, Thaís R. |
author_facet | Souza, Rafael A. C. Martinelli-Kläy, Carla Patrícia d’Acampora, Armando J. Bernardes, Geraldo J. S. Sgrott, Sandro M. Souza, Laila A. C. Lombardi, Tommaso Sudbrack, Thaís R. |
author_sort | Souza, Rafael A. C. |
collection | PubMed |
description | Vascular complication is one of the causes of skin flap healing failure. Sildenafil and tadalafil, a type-5 phosphodiesterase inhibitor, can improve flap viability, however, the action mechanisms involved in this process are still unclear. To assess the effects of orally administered sildenafil and tadalafil on the healing kinetics and skin flap viability, sixty-two Wistar rats were divided into three groups: control (n = 22), sildenafil (n = 20), and tadalafil (n = 20). The solutions were administered orally (dose: 10 mg/kg) immediately after the surgical procedure and then every 24 h. At postoperative days 7 and 14, the skin flap samples were collected, submitted to histological processing and evaluated under optical microscopy. In experimental groups (sildenafil and tadalafil), we found an increased vascularization (p < 0.05) on the 7th and 14th day associated with the ulcer size decrease on the 14th day, although it was not significant. There was a higher influx of neutrophils and a decrease of mononuclear population on the 7th day (p < 0.05). On the 14th day, these differences were observed only in the tadalafil group (p < 0.05). This study suggested positive results with the use of sildenafil and tadalafil as adjuvant drugs in skin flap viability. |
format | Online Article Text |
id | pubmed-8850220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-88502202022-02-23 Effects of sildenafil and tadalafil on skin flap viability Souza, Rafael A. C. Martinelli-Kläy, Carla Patrícia d’Acampora, Armando J. Bernardes, Geraldo J. S. Sgrott, Sandro M. Souza, Laila A. C. Lombardi, Tommaso Sudbrack, Thaís R. Arch Dermatol Res Original Paper Vascular complication is one of the causes of skin flap healing failure. Sildenafil and tadalafil, a type-5 phosphodiesterase inhibitor, can improve flap viability, however, the action mechanisms involved in this process are still unclear. To assess the effects of orally administered sildenafil and tadalafil on the healing kinetics and skin flap viability, sixty-two Wistar rats were divided into three groups: control (n = 22), sildenafil (n = 20), and tadalafil (n = 20). The solutions were administered orally (dose: 10 mg/kg) immediately after the surgical procedure and then every 24 h. At postoperative days 7 and 14, the skin flap samples were collected, submitted to histological processing and evaluated under optical microscopy. In experimental groups (sildenafil and tadalafil), we found an increased vascularization (p < 0.05) on the 7th and 14th day associated with the ulcer size decrease on the 14th day, although it was not significant. There was a higher influx of neutrophils and a decrease of mononuclear population on the 7th day (p < 0.05). On the 14th day, these differences were observed only in the tadalafil group (p < 0.05). This study suggested positive results with the use of sildenafil and tadalafil as adjuvant drugs in skin flap viability. Springer Berlin Heidelberg 2021-03-14 2022 /pmc/articles/PMC8850220/ /pubmed/33715076 http://dx.doi.org/10.1007/s00403-021-02196-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Souza, Rafael A. C. Martinelli-Kläy, Carla Patrícia d’Acampora, Armando J. Bernardes, Geraldo J. S. Sgrott, Sandro M. Souza, Laila A. C. Lombardi, Tommaso Sudbrack, Thaís R. Effects of sildenafil and tadalafil on skin flap viability |
title | Effects of sildenafil and tadalafil on skin flap viability |
title_full | Effects of sildenafil and tadalafil on skin flap viability |
title_fullStr | Effects of sildenafil and tadalafil on skin flap viability |
title_full_unstemmed | Effects of sildenafil and tadalafil on skin flap viability |
title_short | Effects of sildenafil and tadalafil on skin flap viability |
title_sort | effects of sildenafil and tadalafil on skin flap viability |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850220/ https://www.ncbi.nlm.nih.gov/pubmed/33715076 http://dx.doi.org/10.1007/s00403-021-02196-0 |
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