Oregano (Origanum vulgare L.) essential oil provides anti-inflammatory activity and facilitates wound healing in a human keratinocytes cell model.


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
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

111586

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Rosanna Avola (R)

Department of Biomedical and Biotechnological Sciences - Section of Physiology, University of Catania, Via Santa Sofia, 97, 95123, Catania, Italy; Institute of Biomolecular Chemistry, National Research Council (C.N.R.), Via Gaifami, 18, 95026, Catania, Italy.

Giuseppe Granata (G)

Institute of Biomolecular Chemistry, National Research Council (C.N.R.), Via Gaifami, 18, 95026, Catania, Italy.

Corrada Geraci (C)

Institute of Biomolecular Chemistry, National Research Council (C.N.R.), Via Gaifami, 18, 95026, Catania, Italy. Electronic address: corrada.geraci@icb.cnr.it.

Edoardo Napoli (E)

Institute of Biomolecular Chemistry, National Research Council (C.N.R.), Via Gaifami, 18, 95026, Catania, Italy.

Adriana Carol Eleonora Graziano (ACE)

Department of Biomedical and Biotechnological Sciences - Section of Physiology, University of Catania, Via Santa Sofia, 97, 95123, Catania, Italy.

Venera Cardile (V)

Department of Biomedical and Biotechnological Sciences - Section of Physiology, University of Catania, Via Santa Sofia, 97, 95123, Catania, Italy. Electronic address: cardile@unict.it.

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Classifications MeSH