Olive oil-induced reduction of oxidative damage and inflammation promotes wound healing of pressure ulcers in mice

[Display omitted] •Olive oil accelerated ROS and NO synthesis in mice pressure ulcers.•Olive oil decreased inflammatory response and oxidative damage in pressure ulcers.•Olive oil improved re-epithelialization loss in pressure ulcers.•Olive oil accelerated dermal reconstruction and wound closure in...

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Published inJournal of dermatological science Vol. 83; no. 1; pp. 60 - 69
Main Authors Donato-Trancoso, Aline, Monte-Alto-Costa, Andréa, Romana-Souza, Bruna
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ireland Ltd 01.07.2016
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Abstract [Display omitted] •Olive oil accelerated ROS and NO synthesis in mice pressure ulcers.•Olive oil decreased inflammatory response and oxidative damage in pressure ulcers.•Olive oil improved re-epithelialization loss in pressure ulcers.•Olive oil accelerated dermal reconstruction and wound closure in pressure ulcers.•Olive oil improved the wound healing process pressure ulcers, in mice. The overproduction of reactive oxygen species (ROS) and exacerbated inflammatory response are the main events that impair healing of pressure ulcers. Therefore, olive oil may be a good alternative to improve the healing of these chronic lesions due to its anti-inflammatory and antioxidant properties. This study investigated the effect of olive oil administration on wound healing of pressure ulcers in mice. Male Swiss mice were daily treated with olive oil or water until euthanasia. One day after the beginning of treatment, two cycles of ischemia-reperfusion by external application of two magnetic plates were performed in skin to induced pressure ulcer formation. The olive oil administration accelerated ROS and nitric oxide (NO) synthesis and reduced oxidative damage in proteins and lipids when compared to water group. The inflammatory cell infiltration, gene tumor necrosis factor-α (TNF-α) expression and protein neutrophil elastase expression were reduced by olive oil administration when compared to water group. The re-epithelialization and blood vessel number were higher in the olive oil group than in the water group. The olive oil administration accelerated protein expression of TNF-α, active transforming growth factor-β1 and vascular endothelial growth factor-A when compared to water group. The collagen deposition, myofibroblastic differentiation and wound contraction were accelerated by olive oil administration when compared to water group. Olive oil administration improves cutaneous wound healing of pressure ulcers in mice through the acceleration of the ROS and NO synthesis, which reduces oxidative damage and inflammation and promotes dermal reconstruction and wound closure.
AbstractList The overproduction of reactive oxygen species (ROS) and exacerbated inflammatory response are the main events that impair healing of pressure ulcers. Therefore, olive oil may be a good alternative to improve the healing of these chronic lesions due to its anti-inflammatory and antioxidant properties. This study investigated the effect of olive oil administration on wound healing of pressure ulcers in mice. Male Swiss mice were daily treated with olive oil or water until euthanasia. One day after the beginning of treatment, two cycles of ischemia-reperfusion by external application of two magnetic plates were performed in skin to induced pressure ulcer formation. The olive oil administration accelerated ROS and nitric oxide (NO) synthesis and reduced oxidative damage in proteins and lipids when compared to water group. The inflammatory cell infiltration, gene tumor necrosis factor-α (TNF-α) expression and protein neutrophil elastase expression were reduced by olive oil administration when compared to water group. The re-epithelialization and blood vessel number were higher in the olive oil group than in the water group. The olive oil administration accelerated protein expression of TNF-α, active transforming growth factor-β1 and vascular endothelial growth factor-A when compared to water group. The collagen deposition, myofibroblastic differentiation and wound contraction were accelerated by olive oil administration when compared to water group. Olive oil administration improves cutaneous wound healing of pressure ulcers in mice through the acceleration of the ROS and NO synthesis, which reduces oxidative damage and inflammation and promotes dermal reconstruction and wound closure.
The overproduction of reactive oxygen species (ROS) and exacerbated inflammatory response are the main events that impair healing of pressure ulcers. Therefore, olive oil may be a good alternative to improve the healing of these chronic lesions due to its anti-inflammatory and antioxidant properties.BACKGROUNDThe overproduction of reactive oxygen species (ROS) and exacerbated inflammatory response are the main events that impair healing of pressure ulcers. Therefore, olive oil may be a good alternative to improve the healing of these chronic lesions due to its anti-inflammatory and antioxidant properties.This study investigated the effect of olive oil administration on wound healing of pressure ulcers in mice.OBJECTIVEThis study investigated the effect of olive oil administration on wound healing of pressure ulcers in mice.Male Swiss mice were daily treated with olive oil or water until euthanasia. One day after the beginning of treatment, two cycles of ischemia-reperfusion by external application of two magnetic plates were performed in skin to induced pressure ulcer formation.METHODSMale Swiss mice were daily treated with olive oil or water until euthanasia. One day after the beginning of treatment, two cycles of ischemia-reperfusion by external application of two magnetic plates were performed in skin to induced pressure ulcer formation.The olive oil administration accelerated ROS and nitric oxide (NO) synthesis and reduced oxidative damage in proteins and lipids when compared to water group. The inflammatory cell infiltration, gene tumor necrosis factor-α (TNF-α) expression and protein neutrophil elastase expression were reduced by olive oil administration when compared to water group. The re-epithelialization and blood vessel number were higher in the olive oil group than in the water group. The olive oil administration accelerated protein expression of TNF-α, active transforming growth factor-β1 and vascular endothelial growth factor-A when compared to water group. The collagen deposition, myofibroblastic differentiation and wound contraction were accelerated by olive oil administration when compared to water group.RESULTSThe olive oil administration accelerated ROS and nitric oxide (NO) synthesis and reduced oxidative damage in proteins and lipids when compared to water group. The inflammatory cell infiltration, gene tumor necrosis factor-α (TNF-α) expression and protein neutrophil elastase expression were reduced by olive oil administration when compared to water group. The re-epithelialization and blood vessel number were higher in the olive oil group than in the water group. The olive oil administration accelerated protein expression of TNF-α, active transforming growth factor-β1 and vascular endothelial growth factor-A when compared to water group. The collagen deposition, myofibroblastic differentiation and wound contraction were accelerated by olive oil administration when compared to water group.Olive oil administration improves cutaneous wound healing of pressure ulcers in mice through the acceleration of the ROS and NO synthesis, which reduces oxidative damage and inflammation and promotes dermal reconstruction and wound closure.CONCLUSIONOlive oil administration improves cutaneous wound healing of pressure ulcers in mice through the acceleration of the ROS and NO synthesis, which reduces oxidative damage and inflammation and promotes dermal reconstruction and wound closure.
[Display omitted] •Olive oil accelerated ROS and NO synthesis in mice pressure ulcers.•Olive oil decreased inflammatory response and oxidative damage in pressure ulcers.•Olive oil improved re-epithelialization loss in pressure ulcers.•Olive oil accelerated dermal reconstruction and wound closure in pressure ulcers.•Olive oil improved the wound healing process pressure ulcers, in mice. The overproduction of reactive oxygen species (ROS) and exacerbated inflammatory response are the main events that impair healing of pressure ulcers. Therefore, olive oil may be a good alternative to improve the healing of these chronic lesions due to its anti-inflammatory and antioxidant properties. This study investigated the effect of olive oil administration on wound healing of pressure ulcers in mice. Male Swiss mice were daily treated with olive oil or water until euthanasia. One day after the beginning of treatment, two cycles of ischemia-reperfusion by external application of two magnetic plates were performed in skin to induced pressure ulcer formation. The olive oil administration accelerated ROS and nitric oxide (NO) synthesis and reduced oxidative damage in proteins and lipids when compared to water group. The inflammatory cell infiltration, gene tumor necrosis factor-α (TNF-α) expression and protein neutrophil elastase expression were reduced by olive oil administration when compared to water group. The re-epithelialization and blood vessel number were higher in the olive oil group than in the water group. The olive oil administration accelerated protein expression of TNF-α, active transforming growth factor-β1 and vascular endothelial growth factor-A when compared to water group. The collagen deposition, myofibroblastic differentiation and wound contraction were accelerated by olive oil administration when compared to water group. Olive oil administration improves cutaneous wound healing of pressure ulcers in mice through the acceleration of the ROS and NO synthesis, which reduces oxidative damage and inflammation and promotes dermal reconstruction and wound closure.
Graphical abstract
Author Romana-Souza, Bruna
Monte-Alto-Costa, Andréa
Donato-Trancoso, Aline
Author_xml – sequence: 1
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  surname: Romana-Souza
  fullname: Romana-Souza, Bruna
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/27091748$$D View this record in MEDLINE/PubMed
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Issue 1
Keywords NO
MCP-1
Oxidative damage
Pressure ulcer
IR
mRNA
Inflammation
Olive oil
VEGF-A
Cutaneous wound healing
α-SMA
TNF-α
MMP-1
ROS
TGF-β1
cDNA
qPCR
Mice
RFL-10
α-smooth muscle actin
monocyte chemoattractant protein-1
vascular endothelial growth factor-A
complementary DNA
ribosomal protein L 10
messenger RNA
reactive oxygen species
TGF-β 1
transforming growth factor-β1
matrixmetalloproteinase-1
nitric oxide
quantitative polymerase chain reaction
tumor necrosis factor-α
Ischemia-Reperfusion
Language English
License Copyright © 2016 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.
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Snippet [Display omitted] •Olive oil accelerated ROS and NO synthesis in mice pressure ulcers.•Olive oil decreased inflammatory response and oxidative damage in...
Graphical abstract
The overproduction of reactive oxygen species (ROS) and exacerbated inflammatory response are the main events that impair healing of pressure ulcers....
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SubjectTerms Administration, Cutaneous
Animals
Collagen - metabolism
Cutaneous wound healing
Dermatology
Disease Models, Animal
Humans
Inflammation
Inflammation - drug therapy
Male
Mice
Nitric Oxide - metabolism
Olive oil
Olive Oil - administration & dosage
Olive Oil - therapeutic use
Oxidative damage
Pressure ulcer
Pressure Ulcer - drug therapy
Re-Epithelialization - drug effects
Reactive Oxygen Species - metabolism
Skin - blood supply
Skin - drug effects
Skin - metabolism
Transforming Growth Factor beta1 - metabolism
Tumor Necrosis Factor-alpha - metabolism
Vascular Endothelial Growth Factor A - metabolism
Wound Healing - drug effects
Title Olive oil-induced reduction of oxidative damage and inflammation promotes wound healing of pressure ulcers in mice
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https://dx.doi.org/10.1016/j.jdermsci.2016.03.012
https://www.ncbi.nlm.nih.gov/pubmed/27091748
https://www.proquest.com/docview/1795865528
Volume 83
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