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Bromelain Protects Critically Perfused Musculocutaneous Flap Tissue from Necrosis

Bromelain has previously been shown to prevent ischemia-induced necrosis in different types of tissues. In the present study, we, therefore, evaluated for the first time, the tissue-protective effects of bromelain in musculocutaneous flaps in mice. Adult C57BL/6N mice were randomly assigned to a bro...

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Autores principales: Weinzierl, Andrea, Harder, Yves, Schmauss, Daniel, Menger, Michael D., Laschke, Matthias W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9220030/
https://www.ncbi.nlm.nih.gov/pubmed/35740469
http://dx.doi.org/10.3390/biomedicines10061449
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author Weinzierl, Andrea
Harder, Yves
Schmauss, Daniel
Menger, Michael D.
Laschke, Matthias W.
author_facet Weinzierl, Andrea
Harder, Yves
Schmauss, Daniel
Menger, Michael D.
Laschke, Matthias W.
author_sort Weinzierl, Andrea
collection PubMed
description Bromelain has previously been shown to prevent ischemia-induced necrosis in different types of tissues. In the present study, we, therefore, evaluated for the first time, the tissue-protective effects of bromelain in musculocutaneous flaps in mice. Adult C57BL/6N mice were randomly assigned to a bromelain treatment group and a control group. The animals were treated daily with intraperitoneal injections of 20 mg/kg bromelain or saline (control), starting 1 h before the flap elevation throughout a 10-day observation period. The random-pattern musculocutaneous flaps were raised on the backs of the animals and mounted into a dorsal skinfold chamber. Angiogenesis, nutritive blood perfusion and flap necrosis were quantitatively analyzed by means of repeated intravital fluorescence microscopy over 10 days after surgery. After the last microscopy, the flaps were harvested for additional histological and immunohistochemical analyses. Bromelain reduced necrosis of the critically perfused flap tissue by ~25%. The bromelain-treated flaps also exhibited a significantly higher functional microvessel density and an elevated formation of newly developed microvessels in the transition zone between the vital and necrotic tissues when compared to the controls. Immunohistochemical analyses demonstrated a markedly lower invasion of the myeloperoxidase-positive neutrophilic granulocytes and a significantly reduced number of cleaved caspase 3-positive apoptotic cells in the transition zone of bromelain-treated musculocutaneous flaps. These findings indicate that bromelain prevents flap necrosis by maintaining nutritive tissue perfusion and by suppressing ischemia-induced inflammation and apoptosis. Hence, bromelain may represent a promising compound to prevent ischemia-induced flap necrosis in clinical practice.
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spelling pubmed-92200302022-06-24 Bromelain Protects Critically Perfused Musculocutaneous Flap Tissue from Necrosis Weinzierl, Andrea Harder, Yves Schmauss, Daniel Menger, Michael D. Laschke, Matthias W. Biomedicines Article Bromelain has previously been shown to prevent ischemia-induced necrosis in different types of tissues. In the present study, we, therefore, evaluated for the first time, the tissue-protective effects of bromelain in musculocutaneous flaps in mice. Adult C57BL/6N mice were randomly assigned to a bromelain treatment group and a control group. The animals were treated daily with intraperitoneal injections of 20 mg/kg bromelain or saline (control), starting 1 h before the flap elevation throughout a 10-day observation period. The random-pattern musculocutaneous flaps were raised on the backs of the animals and mounted into a dorsal skinfold chamber. Angiogenesis, nutritive blood perfusion and flap necrosis were quantitatively analyzed by means of repeated intravital fluorescence microscopy over 10 days after surgery. After the last microscopy, the flaps were harvested for additional histological and immunohistochemical analyses. Bromelain reduced necrosis of the critically perfused flap tissue by ~25%. The bromelain-treated flaps also exhibited a significantly higher functional microvessel density and an elevated formation of newly developed microvessels in the transition zone between the vital and necrotic tissues when compared to the controls. Immunohistochemical analyses demonstrated a markedly lower invasion of the myeloperoxidase-positive neutrophilic granulocytes and a significantly reduced number of cleaved caspase 3-positive apoptotic cells in the transition zone of bromelain-treated musculocutaneous flaps. These findings indicate that bromelain prevents flap necrosis by maintaining nutritive tissue perfusion and by suppressing ischemia-induced inflammation and apoptosis. Hence, bromelain may represent a promising compound to prevent ischemia-induced flap necrosis in clinical practice. MDPI 2022-06-19 /pmc/articles/PMC9220030/ /pubmed/35740469 http://dx.doi.org/10.3390/biomedicines10061449 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Weinzierl, Andrea
Harder, Yves
Schmauss, Daniel
Menger, Michael D.
Laschke, Matthias W.
Bromelain Protects Critically Perfused Musculocutaneous Flap Tissue from Necrosis
title Bromelain Protects Critically Perfused Musculocutaneous Flap Tissue from Necrosis
title_full Bromelain Protects Critically Perfused Musculocutaneous Flap Tissue from Necrosis
title_fullStr Bromelain Protects Critically Perfused Musculocutaneous Flap Tissue from Necrosis
title_full_unstemmed Bromelain Protects Critically Perfused Musculocutaneous Flap Tissue from Necrosis
title_short Bromelain Protects Critically Perfused Musculocutaneous Flap Tissue from Necrosis
title_sort bromelain protects critically perfused musculocutaneous flap tissue from necrosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9220030/
https://www.ncbi.nlm.nih.gov/pubmed/35740469
http://dx.doi.org/10.3390/biomedicines10061449
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