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 study investigated the anti-inflammatory/oxidative and pro-migratory properties of Phytohustil cough syrup on vascular endothelial cells. Human umbilical vein endothelial cells (HUVEC) were pretreated (24 h) with Phytohustil, its excipients, or REA, followed by incubation with hydrogen peroxide (HO; 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. 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 HO-induced cytotoxicity and intracellular ROS production. Phytohustil and REA significantly stimulated wound closure compared to the control. 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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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773075PMC
http://dx.doi.org/10.3389/fphar.2022.948248DOI Listing

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