Oregano (Origanum vulgare L.) essential oil provides anti-inflammatory activity and facilitates wound healing in a human keratinocytes cell model.
8-Hydroxy-2'-Deoxyguanosine
/ metabolism
Anti-Inflammatory Agents
/ pharmacology
Cyclooxygenase 2
/ metabolism
Histamine
/ metabolism
Humans
Intercellular Adhesion Molecule-1
/ metabolism
Interferon-gamma
/ metabolism
Keratinocytes
/ drug effects
Matrix Metalloproteinases
/ metabolism
Models, Biological
Nitric Oxide Synthase Type II
/ metabolism
Oils, Volatile
/ pharmacology
Origanum
/ chemistry
Reactive Oxygen Species
/ metabolism
Wound Healing
/ drug effects
Healing
In vitro experiments
Keratinocyte
OEO
Oregano
Skin protective activity
Journal
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association
ISSN: 1873-6351
Titre abrégé: Food Chem Toxicol
Pays: England
ID NLM: 8207483
Informations de publication
Date de publication:
Oct 2020
Oct 2020
Historique:
received:
21
05
2020
revised:
15
06
2020
accepted:
06
07
2020
pubmed:
18
7
2020
medline:
22
5
2021
entrez:
18
7
2020
Statut:
ppublish
Résumé
Skin acts as a protective barrier between the body and the external environment. Skin wounds are a common inflammatory disorder for the solution of which plants and essential oils have been applied as a medical option for centuries. Origanum vulgare essential oil (OEO) is largely used in folk medicine, but its molecular mechanisms of action are not fully known. In this study, we evaluated the anti-inflammatory/antioxidant activity as well as wound healing capacity of a well-characterized OEO on human keratinocytes NCTC 2544 treated with interferon-gamma (IFN-γ) and histamine (H) or subjected to a scratch test. The expression of pro-inflammatory mediators such as reactive oxygen species (ROS), inter-cellular adhesion molecule (ICAM)-1, inducible nitric oxide synthase (iNOS), and cyclooxygenase (COX)-2 were verified. The DNA damage was shown by the formation of 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-OHdG) and activation of proliferating cell nuclear antigen (PCNA). Moreover, the abnormal modification of extracellular matrix components (ECM) was examined by determining matrix metalloproteinase (MMP)-1, and -12. Compared to untreated control, OEO showed efficacy in supporting and enhancing the cell motility. In IFN-γ and H treated cells, OEO displayed a significant reduction of ROS, ICAM-1, iNOS, COX-2, 8-OHdG, MMP-1, and MMP-12. OEO proved useful to treat inflammation and support cell motility during wound healing.
Identifiants
pubmed: 32679285
pii: S0278-6915(20)30476-2
doi: 10.1016/j.fct.2020.111586
pii:
doi:
Substances chimiques
Anti-Inflammatory Agents
0
ICAM1 protein, human
0
Oils, Volatile
0
Reactive Oxygen Species
0
Intercellular Adhesion Molecule-1
126547-89-5
Histamine
820484N8I3
Interferon-gamma
82115-62-6
8-Hydroxy-2'-Deoxyguanosine
88847-89-6
NOS2 protein, human
EC 1.14.13.39
Nitric Oxide Synthase Type II
EC 1.14.13.39
Cyclooxygenase 2
EC 1.14.99.1
Matrix Metalloproteinases
EC 3.4.24.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
111586Informations de copyright
Copyright © 2020 Elsevier Ltd. All rights reserved.