Title of article :
An in vitro ethnopharmacological study on Prangos ferulacea: a wound healing agent
Author/Authors :
Fathiazad Fatemeh Drug Applied Research Center - Tabriz University of Medical Sciences - Tabriz, Iran , Yousefi Keyvan Drug Applied Research Center - Tabriz University of Medical Sciences - Tabriz, Iran , Hodaei Darya Drug Applied Research Center - Tabriz University of Medical Sciences - Tabriz, Iran , Hamedeyazdan Sanaz Faculty of Pharmacy - Tabriz University of Medical Sciences - Tabriz, Iran , Lotfipour Farzaneh Department of Drug and Food Control - Faculty of Pharmacy - Tabriz University of Medical Sciences - Tabriz, Iran , Baradaran Behzad Immunology Research Center - Tabriz University of Medical Sciences - Tabriz, Iran , Orangi Mona Immunology Research Center - Tabriz University of Medical Sciences - Tabriz, Iran
Abstract :
Traditionally Prangos ferulacea root
is being used as an effective wound healing agent
especially for pus-filled wounds both in human
and stocks in the western north of Iran. Regarding
the subject we decided to study P. ferulacea roots
essential oil (PFE) for its antimicrobial and wound
healing activities.
Methods: The in vitro wound healing activity of PFE
was evaluated in the mouse fibroblast cell line L929
using MTT assay of cell viability and cytotoxicity
indices. Scratch assay as an in vitro model of wound
healing assay was also conducted in this study. Moreover, the type I collagen content was used as
an indicator of progress in wound healing process using Sircol collagen assay. Besides, PFE was
subjected to GC/MS to identify the chemical constituents, and antimicrobical property was also
evaluated against S. aureus, S. epidermidis, E. coli, P. aeruginosa, S. paratyphi and C. albicans using
agar dilution method.
Results: GC/MS analysis showed that the monoterpene hydrocarbones dominated in PFE,
amounting to a total percentage of 95.1% with the major constituents: β-Phellandrene (32.1%),
m-Tolualdehyde (26.2%), and δ-3-carene (25.8%). PFE inhibited the growth of S. aureus and P.
aeruginusa with the MIC value of 20 μg/mL. In addition, at the second day of treatment, PFE at
concentrations of 4 and 16 μg/mL significantly (P<0.001) enhanced the migration rate of L929
cells by 87.05±2.4 and 63.5±0.08 %, respectively. Moreover, the collagen production by L929 cells
was increased greatly (P<0.001).
Conclusion: It is proposed that the excellent antimicrobial activity along with the significant
increase of migration rate and collagen production by fibroblast cells might be associated with
the high content and synergistic effect of the monoterpens, corroborating the traditional usage of
this plant as a wound healing agent.
Keywords :
Prangos ferulacea , Essential oil , MTT assay , Scratch assay , Sircol collagen assay , Mouse fibroblast cell line
Journal title :
Bioimpacts