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Verapamil‐containing silicone gel reduces scar hypertrophy
A hypertrophic scar is a common dermal fibroproliferative lesion usually treated with topical silicone. Verapamil, a type of calcium channel blocker, is considered a candidate drug for the treatment of hypertrophic scars. Here, we report that the addition of verapamil to topical silicone gel enhance...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450805/ https://www.ncbi.nlm.nih.gov/pubmed/33733593 http://dx.doi.org/10.1111/iwj.13566 |
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author | Choi, Jangyoun Han, Yu Na Rha, Eun Young Kang, Hwi Ju Kim, Ki Joo Park, Il Kyu Kim, Hyun‐Jung Rhie, Jong Won |
author_facet | Choi, Jangyoun Han, Yu Na Rha, Eun Young Kang, Hwi Ju Kim, Ki Joo Park, Il Kyu Kim, Hyun‐Jung Rhie, Jong Won |
author_sort | Choi, Jangyoun |
collection | PubMed |
description | A hypertrophic scar is a common dermal fibroproliferative lesion usually treated with topical silicone. Verapamil, a type of calcium channel blocker, is considered a candidate drug for the treatment of hypertrophic scars. Here, we report that the addition of verapamil to topical silicone gel enhances treatment outcomes of hypertrophic scars. Upon creation of hypertrophic scars with the rabbit ear model, varying concentrations of verapamil‐added silicone gel (0.1, 1, and 10 mg/g) were applied daily for 28 days. After the animals were euthanised, microscopic measurement was performed for (a) scar elevation index (SEI), (b) fibroblast count, and (c) capillary count. On gross analysis, features of hypertrophic scars were significantly alleviated in the verapamil‐added groups. On histologic examination, verapamil‐added groups showed (a) reduced SEI (1.93 (1.79‐2.67) for control vs 1.34 (1.21‐1.51) for silicone only and 1.13 (1.01‐1.65) for verapamil‐added silicone), (b) fibroblast count 700.5 (599.5‐838.5) for control, 613.25 (461‐762.5) for silicone only, and 347.33 (182.5‐527) for verapamil‐added silicone), and (c) capillary formation (52 (35.5‐96.5) for control, 46 (28‐64.5) for silicone only, and 39.83(24‐70) for verapamil‐added silicone) (Kruskal‐Wallis test, P < .05). On western blot, expression levels of collagen I protein was lower in the 1 mg/g and 10 mg/g verapamil‐added silicone compared with control. Therefore, we suggest a therapeutic concentration of verapamil‐added silicone gel of at least over 1 mg/g. Further study regarding maximally effective concentration and deeper insight into the mechanism of action should follow. |
format | Online Article Text |
id | pubmed-8450805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-84508052021-09-27 Verapamil‐containing silicone gel reduces scar hypertrophy Choi, Jangyoun Han, Yu Na Rha, Eun Young Kang, Hwi Ju Kim, Ki Joo Park, Il Kyu Kim, Hyun‐Jung Rhie, Jong Won Int Wound J Original Articles A hypertrophic scar is a common dermal fibroproliferative lesion usually treated with topical silicone. Verapamil, a type of calcium channel blocker, is considered a candidate drug for the treatment of hypertrophic scars. Here, we report that the addition of verapamil to topical silicone gel enhances treatment outcomes of hypertrophic scars. Upon creation of hypertrophic scars with the rabbit ear model, varying concentrations of verapamil‐added silicone gel (0.1, 1, and 10 mg/g) were applied daily for 28 days. After the animals were euthanised, microscopic measurement was performed for (a) scar elevation index (SEI), (b) fibroblast count, and (c) capillary count. On gross analysis, features of hypertrophic scars were significantly alleviated in the verapamil‐added groups. On histologic examination, verapamil‐added groups showed (a) reduced SEI (1.93 (1.79‐2.67) for control vs 1.34 (1.21‐1.51) for silicone only and 1.13 (1.01‐1.65) for verapamil‐added silicone), (b) fibroblast count 700.5 (599.5‐838.5) for control, 613.25 (461‐762.5) for silicone only, and 347.33 (182.5‐527) for verapamil‐added silicone), and (c) capillary formation (52 (35.5‐96.5) for control, 46 (28‐64.5) for silicone only, and 39.83(24‐70) for verapamil‐added silicone) (Kruskal‐Wallis test, P < .05). On western blot, expression levels of collagen I protein was lower in the 1 mg/g and 10 mg/g verapamil‐added silicone compared with control. Therefore, we suggest a therapeutic concentration of verapamil‐added silicone gel of at least over 1 mg/g. Further study regarding maximally effective concentration and deeper insight into the mechanism of action should follow. Blackwell Publishing Ltd 2021-03-17 /pmc/articles/PMC8450805/ /pubmed/33733593 http://dx.doi.org/10.1111/iwj.13566 Text en © 2021 The Authors. International Wound Journal published by Medicalhelplines.com Inc (3M) and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Choi, Jangyoun Han, Yu Na Rha, Eun Young Kang, Hwi Ju Kim, Ki Joo Park, Il Kyu Kim, Hyun‐Jung Rhie, Jong Won Verapamil‐containing silicone gel reduces scar hypertrophy |
title | Verapamil‐containing silicone gel reduces scar hypertrophy |
title_full | Verapamil‐containing silicone gel reduces scar hypertrophy |
title_fullStr | Verapamil‐containing silicone gel reduces scar hypertrophy |
title_full_unstemmed | Verapamil‐containing silicone gel reduces scar hypertrophy |
title_short | Verapamil‐containing silicone gel reduces scar hypertrophy |
title_sort | verapamil‐containing silicone gel reduces scar hypertrophy |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450805/ https://www.ncbi.nlm.nih.gov/pubmed/33733593 http://dx.doi.org/10.1111/iwj.13566 |
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