Antimicrobial activity of flavonoids
Flavonoids are ubiquitous in photosynthesising cells and are commonly found in fruit, vegetables, nuts, seeds, stems, flowers, tea, wine, propolis and honey. For centuries, preparations containing these compounds as the principal physiologically active constituents have been used to treat human dise...
Gespeichert in:
Veröffentlicht in: | International journal of antimicrobial agents 2005-11, Vol.26 (5), p.343-356 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 356 |
---|---|
container_issue | 5 |
container_start_page | 343 |
container_title | International journal of antimicrobial agents |
container_volume | 26 |
creator | Cushnie, T.P. Tim Lamb, Andrew J. |
description | Flavonoids are ubiquitous in photosynthesising cells and are commonly found in fruit, vegetables, nuts, seeds, stems, flowers, tea, wine, propolis and honey. For centuries, preparations containing these compounds as the principal physiologically active constituents have been used to treat human diseases. Increasingly, this class of natural products is becoming the subject of anti-infective research, and many groups have isolated and identified the structures of flavonoids possessing antifungal, antiviral and antibacterial activity. Moreover, several groups have demonstrated synergy between active flavonoids as well as between flavonoids and existing chemotherapeutics. Reports of activity in the field of antibacterial flavonoid research are widely conflicting, probably owing to inter- and intra-assay variation in susceptibility testing. However, several high-quality investigations have examined the relationship between flavonoid structure and antibacterial activity and these are in close agreement. In addition, numerous research groups have sought to elucidate the antibacterial mechanisms of action of selected flavonoids. The activity of quercetin, for example, has been at least partially attributed to inhibition of DNA gyrase. It has also been proposed that sophoraflavone G and (−)-epigallocatechin gallate inhibit cytoplasmic membrane function, and that licochalcones A and C inhibit energy metabolism. Other flavonoids whose mechanisms of action have been investigated include robinetin, myricetin, apigenin, rutin, galangin, 2,4,2′-trihydroxy-5′-methylchalcone and lonchocarpol A. These compounds represent novel leads, and future studies may allow the development of a pharmacologically acceptable antimicrobial agent or class of agents. |
doi_str_mv | 10.1016/j.ijantimicag.2005.09.002 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7127073</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0924857905002554</els_id><sourcerecordid>68854359</sourcerecordid><originalsourceid>FETCH-LOGICAL-c455t-83ffeaa19c48b1d3aca38c39b04919aac7738242d6819d5840a1878248af06673</originalsourceid><addsrcrecordid>eNqNkE1LAzEURYMoWqt_QSqouxnzOUk2ghS_oOBG1-E1k6kp00lNpgX_vSktVneuAsl5N_cdhC4JLgkm1e289HPoer_wFmYlxViUWJcY0wM0IErSQmrCDtEAa8oLJaQ-QacpzTEmgnFxjE5IxSijlR6gq_ttTgxTD-0IbO_Xvv8ahWbUtLAOXfB1OkNHDbTJne_OIXp_fHgbPxeT16eX8f2ksFyIvlCsaRwA0ZarKakZWGDKMj3FXBMNYKVkinJaV4roWiiOIbfNNwoaXFWSDdHdNne5mi5cbV3XR2jNMvoFxC8TwJu_L53_MLOwNpJQiSXLATe7gBg-Vy71ZuGTdW0LnQurZCqlBGdCZ1Bvwbx4StE1P58QbDaOzdz8cmw2jg3WJjvOsxe_W-4nd1IzcL0DIFlomwid9WnPScoUVyJz4y3nstO1d9Ek611nXe2js72pg_9HnW-qF6Bn</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>68854359</pqid></control><display><type>article</type><title>Antimicrobial activity of flavonoids</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Cushnie, T.P. Tim ; Lamb, Andrew J.</creator><creatorcontrib>Cushnie, T.P. Tim ; Lamb, Andrew J.</creatorcontrib><description>Flavonoids are ubiquitous in photosynthesising cells and are commonly found in fruit, vegetables, nuts, seeds, stems, flowers, tea, wine, propolis and honey. For centuries, preparations containing these compounds as the principal physiologically active constituents have been used to treat human diseases. Increasingly, this class of natural products is becoming the subject of anti-infective research, and many groups have isolated and identified the structures of flavonoids possessing antifungal, antiviral and antibacterial activity. Moreover, several groups have demonstrated synergy between active flavonoids as well as between flavonoids and existing chemotherapeutics. Reports of activity in the field of antibacterial flavonoid research are widely conflicting, probably owing to inter- and intra-assay variation in susceptibility testing. However, several high-quality investigations have examined the relationship between flavonoid structure and antibacterial activity and these are in close agreement. In addition, numerous research groups have sought to elucidate the antibacterial mechanisms of action of selected flavonoids. The activity of quercetin, for example, has been at least partially attributed to inhibition of DNA gyrase. It has also been proposed that sophoraflavone G and (−)-epigallocatechin gallate inhibit cytoplasmic membrane function, and that licochalcones A and C inhibit energy metabolism. Other flavonoids whose mechanisms of action have been investigated include robinetin, myricetin, apigenin, rutin, galangin, 2,4,2′-trihydroxy-5′-methylchalcone and lonchocarpol A. These compounds represent novel leads, and future studies may allow the development of a pharmacologically acceptable antimicrobial agent or class of agents.</description><identifier>ISSN: 0924-8579</identifier><identifier>EISSN: 1872-7913</identifier><identifier>DOI: 10.1016/j.ijantimicag.2005.09.002</identifier><identifier>PMID: 16323269</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - pharmacology ; Anti-Infective Agents - chemistry ; Anti-Infective Agents - pharmacology ; Antibacterial ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antifungal ; Antifungal Agents - chemistry ; Antifungal Agents - pharmacology ; Antiviral ; Antiviral Agents - chemistry ; Antiviral Agents - pharmacology ; Biological and medical sciences ; Energy Metabolism - drug effects ; Flavonoids ; Flavonoids - chemistry ; Flavonoids - pharmacology ; Humans ; Mechanism of action ; Medical sciences ; Nucleic Acid Synthesis Inhibitors - chemistry ; Nucleic Acid Synthesis Inhibitors - pharmacology ; Pharmacology. Drug treatments ; Review ; Structure-Activity Relationship ; Structure–activity ; Terminology as Topic</subject><ispartof>International journal of antimicrobial agents, 2005-11, Vol.26 (5), p.343-356</ispartof><rights>2005 Elsevier B.V. and the International Society of Chemotherapy</rights><rights>2005 INIST-CNRS</rights><rights>Copyright © 2005 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved. 2005 Elsevier B.V. and the International Society of Chemotherapy</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c455t-83ffeaa19c48b1d3aca38c39b04919aac7738242d6819d5840a1878248af06673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijantimicag.2005.09.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17238485$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16323269$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cushnie, T.P. Tim</creatorcontrib><creatorcontrib>Lamb, Andrew J.</creatorcontrib><title>Antimicrobial activity of flavonoids</title><title>International journal of antimicrobial agents</title><addtitle>Int J Antimicrob Agents</addtitle><description>Flavonoids are ubiquitous in photosynthesising cells and are commonly found in fruit, vegetables, nuts, seeds, stems, flowers, tea, wine, propolis and honey. For centuries, preparations containing these compounds as the principal physiologically active constituents have been used to treat human diseases. Increasingly, this class of natural products is becoming the subject of anti-infective research, and many groups have isolated and identified the structures of flavonoids possessing antifungal, antiviral and antibacterial activity. Moreover, several groups have demonstrated synergy between active flavonoids as well as between flavonoids and existing chemotherapeutics. Reports of activity in the field of antibacterial flavonoid research are widely conflicting, probably owing to inter- and intra-assay variation in susceptibility testing. However, several high-quality investigations have examined the relationship between flavonoid structure and antibacterial activity and these are in close agreement. In addition, numerous research groups have sought to elucidate the antibacterial mechanisms of action of selected flavonoids. The activity of quercetin, for example, has been at least partially attributed to inhibition of DNA gyrase. It has also been proposed that sophoraflavone G and (−)-epigallocatechin gallate inhibit cytoplasmic membrane function, and that licochalcones A and C inhibit energy metabolism. Other flavonoids whose mechanisms of action have been investigated include robinetin, myricetin, apigenin, rutin, galangin, 2,4,2′-trihydroxy-5′-methylchalcone and lonchocarpol A. These compounds represent novel leads, and future studies may allow the development of a pharmacologically acceptable antimicrobial agent or class of agents.</description><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Anti-Infective Agents - chemistry</subject><subject>Anti-Infective Agents - pharmacology</subject><subject>Antibacterial</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antifungal</subject><subject>Antifungal Agents - chemistry</subject><subject>Antifungal Agents - pharmacology</subject><subject>Antiviral</subject><subject>Antiviral Agents - chemistry</subject><subject>Antiviral Agents - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Energy Metabolism - drug effects</subject><subject>Flavonoids</subject><subject>Flavonoids - chemistry</subject><subject>Flavonoids - pharmacology</subject><subject>Humans</subject><subject>Mechanism of action</subject><subject>Medical sciences</subject><subject>Nucleic Acid Synthesis Inhibitors - chemistry</subject><subject>Nucleic Acid Synthesis Inhibitors - pharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Review</subject><subject>Structure-Activity Relationship</subject><subject>Structure–activity</subject><subject>Terminology as Topic</subject><issn>0924-8579</issn><issn>1872-7913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1LAzEURYMoWqt_QSqouxnzOUk2ghS_oOBG1-E1k6kp00lNpgX_vSktVneuAsl5N_cdhC4JLgkm1e289HPoer_wFmYlxViUWJcY0wM0IErSQmrCDtEAa8oLJaQ-QacpzTEmgnFxjE5IxSijlR6gq_ttTgxTD-0IbO_Xvv8ahWbUtLAOXfB1OkNHDbTJne_OIXp_fHgbPxeT16eX8f2ksFyIvlCsaRwA0ZarKakZWGDKMj3FXBMNYKVkinJaV4roWiiOIbfNNwoaXFWSDdHdNne5mi5cbV3XR2jNMvoFxC8TwJu_L53_MLOwNpJQiSXLATe7gBg-Vy71ZuGTdW0LnQurZCqlBGdCZ1Bvwbx4StE1P58QbDaOzdz8cmw2jg3WJjvOsxe_W-4nd1IzcL0DIFlomwid9WnPScoUVyJz4y3nstO1d9Ek611nXe2js72pg_9HnW-qF6Bn</recordid><startdate>20051101</startdate><enddate>20051101</enddate><creator>Cushnie, T.P. Tim</creator><creator>Lamb, Andrew J.</creator><general>Elsevier B.V</general><general>Elsevier</general><general>Elsevier B.V. and the International Society of Chemotherapy</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20051101</creationdate><title>Antimicrobial activity of flavonoids</title><author>Cushnie, T.P. Tim ; Lamb, Andrew J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-83ffeaa19c48b1d3aca38c39b04919aac7738242d6819d5840a1878248af06673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Anti-Bacterial Agents - chemistry</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Anti-Infective Agents - chemistry</topic><topic>Anti-Infective Agents - pharmacology</topic><topic>Antibacterial</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Antifungal</topic><topic>Antifungal Agents - chemistry</topic><topic>Antifungal Agents - pharmacology</topic><topic>Antiviral</topic><topic>Antiviral Agents - chemistry</topic><topic>Antiviral Agents - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Energy Metabolism - drug effects</topic><topic>Flavonoids</topic><topic>Flavonoids - chemistry</topic><topic>Flavonoids - pharmacology</topic><topic>Humans</topic><topic>Mechanism of action</topic><topic>Medical sciences</topic><topic>Nucleic Acid Synthesis Inhibitors - chemistry</topic><topic>Nucleic Acid Synthesis Inhibitors - pharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Review</topic><topic>Structure-Activity Relationship</topic><topic>Structure–activity</topic><topic>Terminology as Topic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cushnie, T.P. Tim</creatorcontrib><creatorcontrib>Lamb, Andrew J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of antimicrobial agents</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cushnie, T.P. Tim</au><au>Lamb, Andrew J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antimicrobial activity of flavonoids</atitle><jtitle>International journal of antimicrobial agents</jtitle><addtitle>Int J Antimicrob Agents</addtitle><date>2005-11-01</date><risdate>2005</risdate><volume>26</volume><issue>5</issue><spage>343</spage><epage>356</epage><pages>343-356</pages><issn>0924-8579</issn><eissn>1872-7913</eissn><abstract>Flavonoids are ubiquitous in photosynthesising cells and are commonly found in fruit, vegetables, nuts, seeds, stems, flowers, tea, wine, propolis and honey. For centuries, preparations containing these compounds as the principal physiologically active constituents have been used to treat human diseases. Increasingly, this class of natural products is becoming the subject of anti-infective research, and many groups have isolated and identified the structures of flavonoids possessing antifungal, antiviral and antibacterial activity. Moreover, several groups have demonstrated synergy between active flavonoids as well as between flavonoids and existing chemotherapeutics. Reports of activity in the field of antibacterial flavonoid research are widely conflicting, probably owing to inter- and intra-assay variation in susceptibility testing. However, several high-quality investigations have examined the relationship between flavonoid structure and antibacterial activity and these are in close agreement. In addition, numerous research groups have sought to elucidate the antibacterial mechanisms of action of selected flavonoids. The activity of quercetin, for example, has been at least partially attributed to inhibition of DNA gyrase. It has also been proposed that sophoraflavone G and (−)-epigallocatechin gallate inhibit cytoplasmic membrane function, and that licochalcones A and C inhibit energy metabolism. Other flavonoids whose mechanisms of action have been investigated include robinetin, myricetin, apigenin, rutin, galangin, 2,4,2′-trihydroxy-5′-methylchalcone and lonchocarpol A. These compounds represent novel leads, and future studies may allow the development of a pharmacologically acceptable antimicrobial agent or class of agents.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>16323269</pmid><doi>10.1016/j.ijantimicag.2005.09.002</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0924-8579 |
ispartof | International journal of antimicrobial agents, 2005-11, Vol.26 (5), p.343-356 |
issn | 0924-8579 1872-7913 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7127073 |
source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology Anti-Infective Agents - chemistry Anti-Infective Agents - pharmacology Antibacterial Antibiotics. Antiinfectious agents. Antiparasitic agents Antifungal Antifungal Agents - chemistry Antifungal Agents - pharmacology Antiviral Antiviral Agents - chemistry Antiviral Agents - pharmacology Biological and medical sciences Energy Metabolism - drug effects Flavonoids Flavonoids - chemistry Flavonoids - pharmacology Humans Mechanism of action Medical sciences Nucleic Acid Synthesis Inhibitors - chemistry Nucleic Acid Synthesis Inhibitors - pharmacology Pharmacology. Drug treatments Review Structure-Activity Relationship Structure–activity Terminology as Topic |
title | Antimicrobial activity of flavonoids |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T13%3A53%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Antimicrobial%20activity%20of%20flavonoids&rft.jtitle=International%20journal%20of%20antimicrobial%20agents&rft.au=Cushnie,%20T.P.%20Tim&rft.date=2005-11-01&rft.volume=26&rft.issue=5&rft.spage=343&rft.epage=356&rft.pages=343-356&rft.issn=0924-8579&rft.eissn=1872-7913&rft_id=info:doi/10.1016/j.ijantimicag.2005.09.002&rft_dat=%3Cproquest_pubme%3E68854359%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=68854359&rft_id=info:pmid/16323269&rft_els_id=S0924857905002554&rfr_iscdi=true |