Accelerated healing by topical administration of Salvia officinalis essential oil on Pseudomonas aeruginosa and Staphylococcus aureus infected wound model

Accelerative effect of SOO on infected wound healing; (A) by inhibition in bacteria colonization and growth, (B) by up-regulating the expression of IL-1β, IL-6 and TNF-α as pro-inflammatory cytokines and modulating tissue inflammation. (C) by raising the TAC level and reduced MDA content. (D) by up-...

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Veröffentlicht in:Biomedicine & pharmacotherapy 2020-08, Vol.128, p.110120-110120, Article 110120
Hauptverfasser: Farahpour, Mohammad Reza, Pirkhezr, Ehsan, Ashrafian, Ali, Sonboli, Ali
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Pirkhezr, Ehsan
Ashrafian, Ali
Sonboli, Ali
description Accelerative effect of SOO on infected wound healing; (A) by inhibition in bacteria colonization and growth, (B) by up-regulating the expression of IL-1β, IL-6 and TNF-α as pro-inflammatory cytokines and modulating tissue inflammation. (C) by raising the TAC level and reduced MDA content. (D) by up-regulating the VEGF and FGF-2 expression improves the angiogenesis and fibroblasts migrating, respectively. All these alterations resulted in improved collagen biosynthesis and re-epithelialization. [Display omitted] •SOO inhibited bacteria colonization and growth at wound tissue.•SOO enhanced VEGF expression and improved the angiogenesis.•SOO enhanced FGF-2 expression and improved fibroblasts migration.•SOO accelerated collagen biosynthesis and re-epithelialization.•SOO up-regulates the cyclin D1 and Bcl-2 expressions and accelerated cell prolifration. Salvia officinalis L. (Lamiaceae) is known to have antibacterial properties possibly conducive to the healing process of infected wounds. The present study aimed to evaluate the effects of an ointment containing Salvia officinalis essential oil (SOO) on an infected wound model. Essential oil hydrodistillated from the dried leaves of the plant was analyzed by GC-FID and GC–MS. After creating two full-thickness cutaneous wounds, mice were classified into four groups, control, and animals treated with 2 % mupirocin® (standard positive drug), and 2 % and 4 % (w/w) of SOO. In order to evaluate the effects of SOO on the wound healing phases, the expression levels of interleukin-6 (IL-6), interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), cyclin-D1, Bcl-2, fibroblast growth factor-2 (FGF-2) and vascular endothelial growth factors (VEGF) were analyzed using qRT-PCR. Immunohistochemistry analysis, tissue total antioxidant capacity (TAC) and malondialdehyde (MDA) were further assessed in all groups. Concerning essential oil, the main compounds were found to be cis-thujone (26.8 %), camphor (16.4 %), trans-thujone (14.1 %) and 1,8-cineole (10.8 %). Our findings showed that the topical application of SOO was able to shorten the inflammatory phase and accelerate the cellular proliferation, re-vascularization, collagen deposition and re-epithelialization in comparison to the control group (p 
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(C) by raising the TAC level and reduced MDA content. (D) by up-regulating the VEGF and FGF-2 expression improves the angiogenesis and fibroblasts migrating, respectively. All these alterations resulted in improved collagen biosynthesis and re-epithelialization. [Display omitted] •SOO inhibited bacteria colonization and growth at wound tissue.•SOO enhanced VEGF expression and improved the angiogenesis.•SOO enhanced FGF-2 expression and improved fibroblasts migration.•SOO accelerated collagen biosynthesis and re-epithelialization.•SOO up-regulates the cyclin D1 and Bcl-2 expressions and accelerated cell prolifration. Salvia officinalis L. (Lamiaceae) is known to have antibacterial properties possibly conducive to the healing process of infected wounds. The present study aimed to evaluate the effects of an ointment containing Salvia officinalis essential oil (SOO) on an infected wound model. Essential oil hydrodistillated from the dried leaves of the plant was analyzed by GC-FID and GC–MS. After creating two full-thickness cutaneous wounds, mice were classified into four groups, control, and animals treated with 2 % mupirocin® (standard positive drug), and 2 % and 4 % (w/w) of SOO. In order to evaluate the effects of SOO on the wound healing phases, the expression levels of interleukin-6 (IL-6), interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), cyclin-D1, Bcl-2, fibroblast growth factor-2 (FGF-2) and vascular endothelial growth factors (VEGF) were analyzed using qRT-PCR. Immunohistochemistry analysis, tissue total antioxidant capacity (TAC) and malondialdehyde (MDA) were further assessed in all groups. Concerning essential oil, the main compounds were found to be cis-thujone (26.8 %), camphor (16.4 %), trans-thujone (14.1 %) and 1,8-cineole (10.8 %). Our findings showed that the topical application of SOO was able to shorten the inflammatory phase and accelerate the cellular proliferation, re-vascularization, collagen deposition and re-epithelialization in comparison to the control group (p &lt; 0.05). Moreover, increased mRNA levels of FGF-2 and VEGF, and up-regulation of cyclin-D1 and Bcl-2 were observed following the topical application of SOO compared to the control group (p &lt; 0.05). The expression levels of IL-6, IL-1β and TNF-α were reduced in animals treated with SOO on days 3, 7 and 14 (p &lt; 0.05). Administration of SOO increased the TAC level and reduced the MDA content and levels of IL-1β and TNF-α. 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(C) by raising the TAC level and reduced MDA content. (D) by up-regulating the VEGF and FGF-2 expression improves the angiogenesis and fibroblasts migrating, respectively. All these alterations resulted in improved collagen biosynthesis and re-epithelialization. [Display omitted] •SOO inhibited bacteria colonization and growth at wound tissue.•SOO enhanced VEGF expression and improved the angiogenesis.•SOO enhanced FGF-2 expression and improved fibroblasts migration.•SOO accelerated collagen biosynthesis and re-epithelialization.•SOO up-regulates the cyclin D1 and Bcl-2 expressions and accelerated cell prolifration. Salvia officinalis L. (Lamiaceae) is known to have antibacterial properties possibly conducive to the healing process of infected wounds. The present study aimed to evaluate the effects of an ointment containing Salvia officinalis essential oil (SOO) on an infected wound model. Essential oil hydrodistillated from the dried leaves of the plant was analyzed by GC-FID and GC–MS. After creating two full-thickness cutaneous wounds, mice were classified into four groups, control, and animals treated with 2 % mupirocin® (standard positive drug), and 2 % and 4 % (w/w) of SOO. In order to evaluate the effects of SOO on the wound healing phases, the expression levels of interleukin-6 (IL-6), interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), cyclin-D1, Bcl-2, fibroblast growth factor-2 (FGF-2) and vascular endothelial growth factors (VEGF) were analyzed using qRT-PCR. Immunohistochemistry analysis, tissue total antioxidant capacity (TAC) and malondialdehyde (MDA) were further assessed in all groups. Concerning essential oil, the main compounds were found to be cis-thujone (26.8 %), camphor (16.4 %), trans-thujone (14.1 %) and 1,8-cineole (10.8 %). Our findings showed that the topical application of SOO was able to shorten the inflammatory phase and accelerate the cellular proliferation, re-vascularization, collagen deposition and re-epithelialization in comparison to the control group (p &lt; 0.05). Moreover, increased mRNA levels of FGF-2 and VEGF, and up-regulation of cyclin-D1 and Bcl-2 were observed following the topical application of SOO compared to the control group (p &lt; 0.05). The expression levels of IL-6, IL-1β and TNF-α were reduced in animals treated with SOO on days 3, 7 and 14 (p &lt; 0.05). Administration of SOO increased the TAC level and reduced the MDA content and levels of IL-1β and TNF-α. 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Pirkhezr, Ehsan ; Ashrafian, Ali ; Sonboli, Ali</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-b42c89789e01d3d75dabe497b3bf66674eca9b4a2a8e432fe53bc97a238eb1b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Administration, Cutaneous</topic><topic>Angiogenesis</topic><topic>Animals</topic><topic>Anti-Bacterial Agents - administration &amp; dosage</topic><topic>Anti-Bacterial Agents - isolation &amp; purification</topic><topic>Collagen deposition</topic><topic>Cyclin D1 - genetics</topic><topic>Cyclin D1 - metabolism</topic><topic>Cytokines - genetics</topic><topic>Cytokines - metabolism</topic><topic>Disease Models, Animal</topic><topic>Fibroblast Growth Factor 2 - genetics</topic><topic>Fibroblast Growth Factor 2 - metabolism</topic><topic>Infected wound healing</topic><topic>Inflammation</topic><topic>Inflammation Mediators - metabolism</topic><topic>Male</topic><topic>Mice, Inbred BALB C</topic><topic>Oils, Volatile - administration &amp; 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pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Farahpour, Mohammad Reza</au><au>Pirkhezr, Ehsan</au><au>Ashrafian, Ali</au><au>Sonboli, Ali</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Accelerated healing by topical administration of Salvia officinalis essential oil on Pseudomonas aeruginosa and Staphylococcus aureus infected wound model</atitle><jtitle>Biomedicine &amp; pharmacotherapy</jtitle><addtitle>Biomed Pharmacother</addtitle><date>2020-08</date><risdate>2020</risdate><volume>128</volume><spage>110120</spage><epage>110120</epage><pages>110120-110120</pages><artnum>110120</artnum><issn>0753-3322</issn><eissn>1950-6007</eissn><abstract>Accelerative effect of SOO on infected wound healing; (A) by inhibition in bacteria colonization and growth, (B) by up-regulating the expression of IL-1β, IL-6 and TNF-α as pro-inflammatory cytokines and modulating tissue inflammation. (C) by raising the TAC level and reduced MDA content. (D) by up-regulating the VEGF and FGF-2 expression improves the angiogenesis and fibroblasts migrating, respectively. All these alterations resulted in improved collagen biosynthesis and re-epithelialization. [Display omitted] •SOO inhibited bacteria colonization and growth at wound tissue.•SOO enhanced VEGF expression and improved the angiogenesis.•SOO enhanced FGF-2 expression and improved fibroblasts migration.•SOO accelerated collagen biosynthesis and re-epithelialization.•SOO up-regulates the cyclin D1 and Bcl-2 expressions and accelerated cell prolifration. Salvia officinalis L. (Lamiaceae) is known to have antibacterial properties possibly conducive to the healing process of infected wounds. The present study aimed to evaluate the effects of an ointment containing Salvia officinalis essential oil (SOO) on an infected wound model. Essential oil hydrodistillated from the dried leaves of the plant was analyzed by GC-FID and GC–MS. After creating two full-thickness cutaneous wounds, mice were classified into four groups, control, and animals treated with 2 % mupirocin® (standard positive drug), and 2 % and 4 % (w/w) of SOO. In order to evaluate the effects of SOO on the wound healing phases, the expression levels of interleukin-6 (IL-6), interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), cyclin-D1, Bcl-2, fibroblast growth factor-2 (FGF-2) and vascular endothelial growth factors (VEGF) were analyzed using qRT-PCR. Immunohistochemistry analysis, tissue total antioxidant capacity (TAC) and malondialdehyde (MDA) were further assessed in all groups. Concerning essential oil, the main compounds were found to be cis-thujone (26.8 %), camphor (16.4 %), trans-thujone (14.1 %) and 1,8-cineole (10.8 %). Our findings showed that the topical application of SOO was able to shorten the inflammatory phase and accelerate the cellular proliferation, re-vascularization, collagen deposition and re-epithelialization in comparison to the control group (p &lt; 0.05). Moreover, increased mRNA levels of FGF-2 and VEGF, and up-regulation of cyclin-D1 and Bcl-2 were observed following the topical application of SOO compared to the control group (p &lt; 0.05). The expression levels of IL-6, IL-1β and TNF-α were reduced in animals treated with SOO on days 3, 7 and 14 (p &lt; 0.05). Administration of SOO increased the TAC level and reduced the MDA content and levels of IL-1β and TNF-α. It is concluded that SOO is able to accelerate the wound healing process by regulating the expression of pro-inflammatory cytokines, growth factors, and antioxidant properties.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>32460189</pmid><doi>10.1016/j.biopha.2020.110120</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Administration, Cutaneous
Angiogenesis
Animals
Anti-Bacterial Agents - administration & dosage
Anti-Bacterial Agents - isolation & purification
Collagen deposition
Cyclin D1 - genetics
Cyclin D1 - metabolism
Cytokines - genetics
Cytokines - metabolism
Disease Models, Animal
Fibroblast Growth Factor 2 - genetics
Fibroblast Growth Factor 2 - metabolism
Infected wound healing
Inflammation
Inflammation Mediators - metabolism
Male
Mice, Inbred BALB C
Oils, Volatile - administration & dosage
Oils, Volatile - isolation & purification
Plant Oils - administration & dosage
Plant Oils - isolation & purification
Proto-Oncogene Proteins c-bcl-2 - genetics
Proto-Oncogene Proteins c-bcl-2 - metabolism
Pseudomonas Infections - drug therapy
Pseudomonas Infections - metabolism
Pseudomonas Infections - microbiology
Pseudomonas Infections - pathology
Re-epithelialization
Salvia officinalis - chemistry
Salvia officinalis essential oil
Staphylococcal Infections - drug therapy
Staphylococcal Infections - metabolism
Staphylococcal Infections - microbiology
Staphylococcal Infections - pathology
Time Factors
Vascular Endothelial Growth Factor A - genetics
Vascular Endothelial Growth Factor A - metabolism
Wound Healing - drug effects
Wound Infection - drug therapy
Wound Infection - metabolism
Wound Infection - microbiology
Wound Infection - pathology
title Accelerated healing by topical administration of Salvia officinalis essential oil on Pseudomonas aeruginosa and Staphylococcus aureus infected wound model
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