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Phytohustil(®) and root extract of Althaea officinalis L. exert anti-inflammatory and anti-oxidative properties and improve the migratory capacity of endothelial cells in vitro

Introduction: Althaea officinalis L.'s root extract (REA) has been used as a medicinal plant since ancient times to treat a cough. Applying REA leads to a protective film that induces a faster regeneration of the lesioned laryngopharyngeal mucosa caused by dry coughs. The buccopharyngeal mucosa...

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Autores principales: Bonaterra, Gabriel A., Schmitt, Johanna, Schneider, Kim, Schwarzbach, Hans, Aziz-Kalbhenn, Heba, Kelber, Olaf, Müller, Jürgen, Kinscherf, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773075/
https://www.ncbi.nlm.nih.gov/pubmed/36569306
http://dx.doi.org/10.3389/fphar.2022.948248
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author Bonaterra, Gabriel A.
Schmitt, Johanna
Schneider, Kim
Schwarzbach, Hans
Aziz-Kalbhenn, Heba
Kelber, Olaf
Müller, Jürgen
Kinscherf, Ralf
author_facet Bonaterra, Gabriel A.
Schmitt, Johanna
Schneider, Kim
Schwarzbach, Hans
Aziz-Kalbhenn, Heba
Kelber, Olaf
Müller, Jürgen
Kinscherf, Ralf
author_sort Bonaterra, Gabriel A.
collection PubMed
description Introduction: Althaea officinalis L.'s root extract (REA) has been used as a medicinal plant since ancient times to treat a cough. Applying REA leads to a protective film that induces a faster regeneration of the lesioned laryngopharyngeal mucosa caused by dry coughs. The buccopharyngeal mucosa is a highly vascularized tissue. In this regard, anti-inflammatory/-oxidant phytochemicals that improve the repair of the lesion site, e.g., neovascularization in the wound, are critical for promoting healing. For this reason, it is essential to investigate the effects of Phytohustil(®) and REA on different cellular components of the mucosa under conditions similar to those found in the injured mucosa. Thus, this in vitro study investigated the anti-inflammatory/oxidative and pro-migratory properties of Phytohustil(®) cough syrup on vascular endothelial cells. Methods: Human umbilical vein endothelial cells (HUVEC) were pretreated (24 h) with Phytohustil(®), its excipients, or REA, followed by incubation with hydrogen peroxide (H(2)O(2); 1 h; pro-oxidative) or with lipopolysaccharides (LPS; 3 h; pro-inflammatory). Viability and cytotoxicity were measured by PrestoBlue(®) assay. Intracellular reactive oxygen species (ROS) were quantified with 20-70-dichlorofluorescein diacetate (DCFDA). The release of interleukin 6 (IL6) was determined by enzyme-linked immunosorbent assay (ELISA). The migratory capacity of HUVEC was measured using a scratch assay. Results: Our results show that Phytohustil(®), its excipients and REA were not cytotoxic. Pretreatment of HUVEC (24 h) with Phytohustil(®) or REA inhibited the LPS-activated IL6 release. Phytohustil(®) or REA inhibited the H(2)O(2)-induced cytotoxicity and intracellular ROS production. Phytohustil(®) and REA significantly stimulated wound closure compared to the control. Conclusion: Our data show that Phytohustil(®) and REA have anti-inflammatory/-oxidant properties and improve the migratory capacity of vascular endothelial cells. These properties may contribute to the healing characteristics of Phytohustil(®) and support the benefit of Phytohustil(®) in patient’s treatment of irritated oral mucosa.
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spelling pubmed-97730752022-12-23 Phytohustil(®) and root extract of Althaea officinalis L. exert anti-inflammatory and anti-oxidative properties and improve the migratory capacity of endothelial cells in vitro Bonaterra, Gabriel A. Schmitt, Johanna Schneider, Kim Schwarzbach, Hans Aziz-Kalbhenn, Heba Kelber, Olaf Müller, Jürgen Kinscherf, Ralf Front Pharmacol Pharmacology Introduction: Althaea officinalis L.'s root extract (REA) has been used as a medicinal plant since ancient times to treat a cough. Applying REA leads to a protective film that induces a faster regeneration of the lesioned laryngopharyngeal mucosa caused by dry coughs. The buccopharyngeal mucosa is a highly vascularized tissue. In this regard, anti-inflammatory/-oxidant phytochemicals that improve the repair of the lesion site, e.g., neovascularization in the wound, are critical for promoting healing. For this reason, it is essential to investigate the effects of Phytohustil(®) and REA on different cellular components of the mucosa under conditions similar to those found in the injured mucosa. Thus, this in vitro study investigated the anti-inflammatory/oxidative and pro-migratory properties of Phytohustil(®) cough syrup on vascular endothelial cells. Methods: Human umbilical vein endothelial cells (HUVEC) were pretreated (24 h) with Phytohustil(®), its excipients, or REA, followed by incubation with hydrogen peroxide (H(2)O(2); 1 h; pro-oxidative) or with lipopolysaccharides (LPS; 3 h; pro-inflammatory). Viability and cytotoxicity were measured by PrestoBlue(®) assay. Intracellular reactive oxygen species (ROS) were quantified with 20-70-dichlorofluorescein diacetate (DCFDA). The release of interleukin 6 (IL6) was determined by enzyme-linked immunosorbent assay (ELISA). The migratory capacity of HUVEC was measured using a scratch assay. Results: Our results show that Phytohustil(®), its excipients and REA were not cytotoxic. Pretreatment of HUVEC (24 h) with Phytohustil(®) or REA inhibited the LPS-activated IL6 release. Phytohustil(®) or REA inhibited the H(2)O(2)-induced cytotoxicity and intracellular ROS production. Phytohustil(®) and REA significantly stimulated wound closure compared to the control. Conclusion: Our data show that Phytohustil(®) and REA have anti-inflammatory/-oxidant properties and improve the migratory capacity of vascular endothelial cells. These properties may contribute to the healing characteristics of Phytohustil(®) and support the benefit of Phytohustil(®) in patient’s treatment of irritated oral mucosa. Frontiers Media S.A. 2022-12-08 /pmc/articles/PMC9773075/ /pubmed/36569306 http://dx.doi.org/10.3389/fphar.2022.948248 Text en Copyright © 2022 Bonaterra, Schmitt, Schneider, Schwarzbach, Aziz-Kalbhenn, Kelber, Müller and Kinscherf. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Bonaterra, Gabriel A.
Schmitt, Johanna
Schneider, Kim
Schwarzbach, Hans
Aziz-Kalbhenn, Heba
Kelber, Olaf
Müller, Jürgen
Kinscherf, Ralf
Phytohustil(®) and root extract of Althaea officinalis L. exert anti-inflammatory and anti-oxidative properties and improve the migratory capacity of endothelial cells in vitro
title Phytohustil(®) and root extract of Althaea officinalis L. exert anti-inflammatory and anti-oxidative properties and improve the migratory capacity of endothelial cells in vitro
title_full Phytohustil(®) and root extract of Althaea officinalis L. exert anti-inflammatory and anti-oxidative properties and improve the migratory capacity of endothelial cells in vitro
title_fullStr Phytohustil(®) and root extract of Althaea officinalis L. exert anti-inflammatory and anti-oxidative properties and improve the migratory capacity of endothelial cells in vitro
title_full_unstemmed Phytohustil(®) and root extract of Althaea officinalis L. exert anti-inflammatory and anti-oxidative properties and improve the migratory capacity of endothelial cells in vitro
title_short Phytohustil(®) and root extract of Althaea officinalis L. exert anti-inflammatory and anti-oxidative properties and improve the migratory capacity of endothelial cells in vitro
title_sort phytohustil(®) and root extract of althaea officinalis l. exert anti-inflammatory and anti-oxidative properties and improve the migratory capacity of endothelial cells in vitro
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773075/
https://www.ncbi.nlm.nih.gov/pubmed/36569306
http://dx.doi.org/10.3389/fphar.2022.948248
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