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Potential anti-inflammatory, antioxidant and antimicrobial activities of Sambucus australis

Context: Sambucus australis Cham. & Schltdl. (Adoxaceae) is used in Brazilian folk medicine to treat inflammatory disorders. Objective: To evaluate the in vitro anti-inflammatory, antioxidant and antimicrobial properties of S. australis. Materials and methods: The anti-inflammatory activity of et...

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Published in:Pharmaceutical biology 2017-01, Vol.55 (1), p.991-997
Main Authors: Benevides Bahiense, Jhéssica, Marques, Franciane Martins, Figueira, Mariana Moreira, Vargas, Thais Souza, Kondratyuk, Tamara P., Endringer, Denise Coutinho, Scherer, Rodrigo, Fronza, Marcio
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cited_by cdi_FETCH-LOGICAL-c562t-88fc4011214cd388f8129f462eef86c5d269f65527ddc7e5dc420ce3b2ea104c3
cites cdi_FETCH-LOGICAL-c562t-88fc4011214cd388f8129f462eef86c5d269f65527ddc7e5dc420ce3b2ea104c3
container_end_page 997
container_issue 1
container_start_page 991
container_title Pharmaceutical biology
container_volume 55
creator Benevides Bahiense, Jhéssica
Marques, Franciane Martins
Figueira, Mariana Moreira
Vargas, Thais Souza
Kondratyuk, Tamara P.
Endringer, Denise Coutinho
Scherer, Rodrigo
Fronza, Marcio
description Context: Sambucus australis Cham. & Schltdl. (Adoxaceae) is used in Brazilian folk medicine to treat inflammatory disorders. Objective: To evaluate the in vitro anti-inflammatory, antioxidant and antimicrobial properties of S. australis. Materials and methods: The anti-inflammatory activity of ethanol extracts of the leaf and bark of S. australis (1-100 μg/mL) were studied in lipopolysaccharide/interferon γ stimulated murine macrophages RAW 264.7 cells (24 h incubation) by investigating the release of nitric oxide (NO) and tumour necrosis factor-alpha (TNF-α) and in the TNF-α-induced nuclear factor kappa (NF-κB) assay. Minimum inhibitory concentration (MIC) was determined by the microdilution test (24 h incubation). Antioxidant activity was determined by 2,2-diphenyl-1-picrylhydrazyl (DPPH), ferric reducing antioxidant power (FRAP) and the NO scavenging assays. Chemical composition was assessed by LC-MS/MS. Results: Antioxidant activities in the DPPH (IC 50 43.5 and 66.2 μg/mL), FRAP (IC 50 312.6 and 568.3 μg/mL) and NO radical scavenging assays (IC 50 285.0 and 972.6 μg/mL) were observed in the leaf and bark ethanol extracts, respectively. Solely the leaf extract showed significant inhibition of NO and TNF-α production in RAW264.7 cells at concentrations of 2 and 100 μg/mL, respectively, and suppression of TNF-α inhibition of NF-κB by 12.8 and 20.4% at concentrations of 50 and 100 μg/mL, respectively. The extract also exhibited antibacterial activity against Salmonella typhimurium (MIC 250 μg/mL) and Klebsiella pneumoniae (MIC 250 μg/mL). LC-MS/MS revealed the presence of chlorogenic acid and rutin as major compounds. Discussion and conclusion: The results indicate that the ethanol leaf extract of S. australis exhibit prominent anti-inflammatory effects.
doi_str_mv 10.1080/13880209.2017.1285324
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(Adoxaceae) is used in Brazilian folk medicine to treat inflammatory disorders. Objective: To evaluate the in vitro anti-inflammatory, antioxidant and antimicrobial properties of S. australis. Materials and methods: The anti-inflammatory activity of ethanol extracts of the leaf and bark of S. australis (1-100 μg/mL) were studied in lipopolysaccharide/interferon γ stimulated murine macrophages RAW 264.7 cells (24 h incubation) by investigating the release of nitric oxide (NO) and tumour necrosis factor-alpha (TNF-α) and in the TNF-α-induced nuclear factor kappa (NF-κB) assay. Minimum inhibitory concentration (MIC) was determined by the microdilution test (24 h incubation). Antioxidant activity was determined by 2,2-diphenyl-1-picrylhydrazyl (DPPH), ferric reducing antioxidant power (FRAP) and the NO scavenging assays. Chemical composition was assessed by LC-MS/MS. Results: Antioxidant activities in the DPPH (IC 50 43.5 and 66.2 μg/mL), FRAP (IC 50 312.6 and 568.3 μg/mL) and NO radical scavenging assays (IC 50 285.0 and 972.6 μg/mL) were observed in the leaf and bark ethanol extracts, respectively. Solely the leaf extract showed significant inhibition of NO and TNF-α production in RAW264.7 cells at concentrations of 2 and 100 μg/mL, respectively, and suppression of TNF-α inhibition of NF-κB by 12.8 and 20.4% at concentrations of 50 and 100 μg/mL, respectively. The extract also exhibited antibacterial activity against Salmonella typhimurium (MIC 250 μg/mL) and Klebsiella pneumoniae (MIC 250 μg/mL). LC-MS/MS revealed the presence of chlorogenic acid and rutin as major compounds. 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Published by Informa UK Limited, trading as Taylor &amp; Francis Group. 2017</rights><rights>2017 The Author(s). Published by Informa UK Limited, trading as Taylor &amp; Francis Group. This work is licensed under the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2017 The Author(s). 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(Adoxaceae) is used in Brazilian folk medicine to treat inflammatory disorders. Objective: To evaluate the in vitro anti-inflammatory, antioxidant and antimicrobial properties of S. australis. Materials and methods: The anti-inflammatory activity of ethanol extracts of the leaf and bark of S. australis (1-100 μg/mL) were studied in lipopolysaccharide/interferon γ stimulated murine macrophages RAW 264.7 cells (24 h incubation) by investigating the release of nitric oxide (NO) and tumour necrosis factor-alpha (TNF-α) and in the TNF-α-induced nuclear factor kappa (NF-κB) assay. Minimum inhibitory concentration (MIC) was determined by the microdilution test (24 h incubation). Antioxidant activity was determined by 2,2-diphenyl-1-picrylhydrazyl (DPPH), ferric reducing antioxidant power (FRAP) and the NO scavenging assays. Chemical composition was assessed by LC-MS/MS. Results: Antioxidant activities in the DPPH (IC 50 43.5 and 66.2 μg/mL), FRAP (IC 50 312.6 and 568.3 μg/mL) and NO radical scavenging assays (IC 50 285.0 and 972.6 μg/mL) were observed in the leaf and bark ethanol extracts, respectively. Solely the leaf extract showed significant inhibition of NO and TNF-α production in RAW264.7 cells at concentrations of 2 and 100 μg/mL, respectively, and suppression of TNF-α inhibition of NF-κB by 12.8 and 20.4% at concentrations of 50 and 100 μg/mL, respectively. The extract also exhibited antibacterial activity against Salmonella typhimurium (MIC 250 μg/mL) and Klebsiella pneumoniae (MIC 250 μg/mL). LC-MS/MS revealed the presence of chlorogenic acid and rutin as major compounds. 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purification</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Leaves</topic><topic>Plants, Medicinal</topic><topic>RAW 264.7 Cells</topic><topic>Rutin</topic><topic>Rutin - isolation &amp; purification</topic><topic>Rutin - pharmacology</topic><topic>Salmonella typhimurium - drug effects</topic><topic>Salmonella typhimurium - growth &amp; development</topic><topic>Sambucus</topic><topic>Sambucus - chemistry</topic><topic>Solvents - chemistry</topic><topic>Swiss 3T3 Cells</topic><topic>Transfection</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumor necrosis factor-α</topic><topic>Tumors</topic><topic>γ-Interferon</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Benevides Bahiense, Jhéssica</creatorcontrib><creatorcontrib>Marques, Franciane Martins</creatorcontrib><creatorcontrib>Figueira, Mariana Moreira</creatorcontrib><creatorcontrib>Vargas, Thais Souza</creatorcontrib><creatorcontrib>Kondratyuk, Tamara P.</creatorcontrib><creatorcontrib>Endringer, Denise Coutinho</creatorcontrib><creatorcontrib>Scherer, Rodrigo</creatorcontrib><creatorcontrib>Fronza, Marcio</creatorcontrib><collection>Taylor &amp; 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Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Pharmaceutical biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Benevides Bahiense, Jhéssica</au><au>Marques, Franciane Martins</au><au>Figueira, Mariana Moreira</au><au>Vargas, Thais Souza</au><au>Kondratyuk, Tamara P.</au><au>Endringer, Denise Coutinho</au><au>Scherer, Rodrigo</au><au>Fronza, Marcio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Potential anti-inflammatory, antioxidant and antimicrobial activities of Sambucus australis</atitle><jtitle>Pharmaceutical biology</jtitle><addtitle>Pharm Biol</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>55</volume><issue>1</issue><spage>991</spage><epage>997</epage><pages>991-997</pages><issn>1388-0209</issn><eissn>1744-5116</eissn><abstract>Context: Sambucus australis Cham. &amp; Schltdl. (Adoxaceae) is used in Brazilian folk medicine to treat inflammatory disorders. Objective: To evaluate the in vitro anti-inflammatory, antioxidant and antimicrobial properties of S. australis. Materials and methods: The anti-inflammatory activity of ethanol extracts of the leaf and bark of S. australis (1-100 μg/mL) were studied in lipopolysaccharide/interferon γ stimulated murine macrophages RAW 264.7 cells (24 h incubation) by investigating the release of nitric oxide (NO) and tumour necrosis factor-alpha (TNF-α) and in the TNF-α-induced nuclear factor kappa (NF-κB) assay. Minimum inhibitory concentration (MIC) was determined by the microdilution test (24 h incubation). Antioxidant activity was determined by 2,2-diphenyl-1-picrylhydrazyl (DPPH), ferric reducing antioxidant power (FRAP) and the NO scavenging assays. Chemical composition was assessed by LC-MS/MS. Results: Antioxidant activities in the DPPH (IC 50 43.5 and 66.2 μg/mL), FRAP (IC 50 312.6 and 568.3 μg/mL) and NO radical scavenging assays (IC 50 285.0 and 972.6 μg/mL) were observed in the leaf and bark ethanol extracts, respectively. Solely the leaf extract showed significant inhibition of NO and TNF-α production in RAW264.7 cells at concentrations of 2 and 100 μg/mL, respectively, and suppression of TNF-α inhibition of NF-κB by 12.8 and 20.4% at concentrations of 50 and 100 μg/mL, respectively. The extract also exhibited antibacterial activity against Salmonella typhimurium (MIC 250 μg/mL) and Klebsiella pneumoniae (MIC 250 μg/mL). LC-MS/MS revealed the presence of chlorogenic acid and rutin as major compounds. Discussion and conclusion: The results indicate that the ethanol leaf extract of S. australis exhibit prominent anti-inflammatory effects.</abstract><cop>England</cop><pub>Taylor &amp; Francis</pub><pmid>28166708</pmid><doi>10.1080/13880209.2017.1285324</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-9396-2097</orcidid><orcidid>https://orcid.org/0000-0001-7656-0248</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1388-0209
ispartof Pharmaceutical biology, 2017-01, Vol.55 (1), p.991-997
issn 1388-0209
1744-5116
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6130686
source Taylor & Francis Open Access; PubMed Central
subjects Animals
Anti-Infective Agents - chemistry
Anti-Infective Agents - isolation & purification
Anti-Infective Agents - pharmacology
Anti-Inflammatory Agents - chemistry
Anti-Inflammatory Agents - isolation & purification
Anti-Inflammatory Agents - pharmacology
Antibacterial activity
Antimicrobial agents
Antioxidants
Antioxidants - chemistry
Antioxidants - isolation & purification
Antioxidants - pharmacology
Bark
Biphenyl Compounds - chemistry
Chlorides - chemistry
Chlorogenic acid
Chlorogenic Acid - isolation & purification
Chlorogenic Acid - pharmacology
cytokines
Dose-Response Relationship, Drug
Ethanol
Ethanol - chemistry
Ferric Compounds - chemistry
HEK293 Cells
Humans
Inflammation Mediators - metabolism
Inflammatory diseases
Klebsiella pneumoniae - drug effects
Klebsiella pneumoniae - growth & development
Leaves
Lipopolysaccharides
Lipopolysaccharides - pharmacology
Macrophages
Macrophages - drug effects
Macrophages - metabolism
Mice
Microbial Sensitivity Tests
Minimum inhibitory concentration
Natural products
NF-kappa B - genetics
NF-kappa B - metabolism
NF-κB protein
Nitric oxide
Nitric Oxide - metabolism
nuclear factor-κB
Oxidation-Reduction
phenolic compounds
Phytotherapy
Picrates - chemistry
Plant Bark
Plant extracts
Plant Extracts - chemistry
Plant Extracts - isolation & purification
Plant Extracts - pharmacology
Plant Leaves
Plants, Medicinal
RAW 264.7 Cells
Rutin
Rutin - isolation & purification
Rutin - pharmacology
Salmonella typhimurium - drug effects
Salmonella typhimurium - growth & development
Sambucus
Sambucus - chemistry
Solvents - chemistry
Swiss 3T3 Cells
Transfection
Tumor Necrosis Factor-alpha - metabolism
Tumor necrosis factor-TNF
Tumor necrosis factor-α
Tumors
γ-Interferon
title Potential anti-inflammatory, antioxidant and antimicrobial activities of Sambucus australis
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