Antiviral activity of Aloe hijazensis against some haemagglutinating viruses infection and its phytoconstituents
Identifieur interne : 000F11 ( Istex/Corpus ); précédent : 000F10; suivant : 000F12Antiviral activity of Aloe hijazensis against some haemagglutinating viruses infection and its phytoconstituents
Auteurs : Howaida I. Abd-Alla ; Nagat S. Abu-Gabal ; Amal Z. Hassan ; Mounir M. El-Safty ; Nagwa M. M. ShalabySource :
- Archives of Pharmacal Research [ 0253-6269 ] ; 2012-08-01.
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Abstract
Abstract: Evaluation of the antiviral activities of flowers, flower-peduncles, leaves, and roots of Aloe hijazensis against haemagglutinating viruses of avian paramyxovirus type-1 (APMV-1), avian influenza virus type A (AI-H5N1), Newcastle disease virus (NDV), and egg-drop syndrome virus (EDSV) in specific pathogen free (SPF) chicken embryos were carried out. Extract of the flowers and leaves showed relatively higher activity than the extracts of other plant parts. Thirteen compounds were isolated from both the flowers and flower-peduncles of A. hijazensis. The isolated compounds were classified into: five anthraquinones; ziganein, ziganein-5-methyl ether, aloesaponarin I, chrysophanol, aloe-emodin, one dihydroisocoumarin; feralolide, four flavonoids; homoplantaginin, isoorientin, luteolin 7-glucuronopyranoside, isovitexin, one phenolic acid; p-coumaric acid, the anthrone; barbaloin together with aloenin. Eleven compounds were attributed to the flowers and seven to the flower-peduncles. Homoplantaginin and luteolin 7-glucuronopyranoside are reported here for the first time from Aloe spp. To the best of our knowledge, this is the first report on the chemical composition and biological activity of those plant parts.
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DOI: 10.1007/s12272-012-0804-5
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Extract of the flowers and leaves showed relatively higher activity than the extracts of other plant parts. Thirteen compounds were isolated from both the flowers and flower-peduncles of A. hijazensis. The isolated compounds were classified into: five anthraquinones; ziganein, ziganein-5-methyl ether, aloesaponarin I, chrysophanol, aloe-emodin, one dihydroisocoumarin; feralolide, four flavonoids; homoplantaginin, isoorientin, luteolin 7-glucuronopyranoside, isovitexin, one phenolic acid; p-coumaric acid, the anthrone; barbaloin together with aloenin. Eleven compounds were attributed to the flowers and seven to the flower-peduncles. Homoplantaginin and luteolin 7-glucuronopyranoside are reported here for the first time from Aloe spp. To the best of our knowledge, this is the first report on the chemical composition and biological activity of those plant parts.</div></front></TEI><istex><corpusName>springer-journals</corpusName><author><json:item><name>Howaida I. 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Extract of the flowers and leaves showed relatively higher activity than the extracts of other plant parts. Thirteen compounds were isolated from both the flowers and flower-peduncles of A. hijazensis. The isolated compounds were classified into: five anthraquinones; ziganein, ziganein-5-methyl ether, aloesaponarin I, chrysophanol, aloe-emodin, one dihydroisocoumarin; feralolide, four flavonoids; homoplantaginin, isoorientin, luteolin 7-glucuronopyranoside, isovitexin, one phenolic acid; p-coumaric acid, the anthrone; barbaloin together with aloenin. Eleven compounds were attributed to the flowers and seven to the flower-peduncles. 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Extract of the flowers and leaves showed relatively higher activity than the extracts of other plant parts. Thirteen compounds were isolated from both the flowers and flower-peduncles of A. hijazensis. The isolated compounds were classified into: five anthraquinones; ziganein, ziganein-5-methyl ether, aloesaponarin I, chrysophanol, aloe-emodin, one dihydroisocoumarin; feralolide, four flavonoids; homoplantaginin, isoorientin, luteolin 7-glucuronopyranoside, isovitexin, one phenolic acid; p-coumaric acid, the anthrone; barbaloin together with aloenin. Eleven compounds were attributed to the flowers and seven to the flower-peduncles. Homoplantaginin and luteolin 7-glucuronopyranoside are reported here for the first time from Aloe spp. To the best of our knowledge, this is the first report on the chemical composition and biological activity of those plant parts.</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>Key words</head><item><term>Aloe hijazensis</term></item><item><term>Haemagglutinating viruses</term></item><item><term>Phytochemical constituents</term></item></list></keywords></textClass><textClass><keywords scheme="Journal-Subject-Collection"><list><label>Medicine</label><item><term>SC11</term></item></list></keywords></textClass><textClass><keywords scheme="Journal Subject"><list><head>Pharmacy</head><item><term>Pharmacology/Toxicology</term></item><item><term>Pharmacy</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2011-08-26">Created</change><change when="2012-08-01">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/VQC-0RQK9GTV-B/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="corpus springer-journals not found" wicri:toSee="no header"><istex:xmlDeclaration>version="1.0" encoding="UTF-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//Springer-Verlag//DTD A++ V2.4//EN" URI="http://devel.springer.de/A++/V2.4/DTD/A++V2.4.dtd" name="istex:docType"></istex:docType><istex:document><Publisher><PublisherInfo><PublisherName>Pharmaceutical Society of Korea</PublisherName><PublisherLocation>Heidelberg</PublisherLocation></PublisherInfo><Journal OutputMedium="All"><JournalInfo JournalProductType="ArchiveJournal" NumberingStyle="Unnumbered"><JournalID>12272</JournalID><JournalPrintISSN>0253-6269</JournalPrintISSN><JournalElectronicISSN>1976-3786</JournalElectronicISSN><JournalTitle>Archives of Pharmacal Research</JournalTitle><JournalAbbreviatedTitle>Arch. 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Res.</JournalAbbreviatedTitle><JournalSubjectGroup><JournalSubject Type="Primary">Pharmacy</JournalSubject><JournalSubject Type="Secondary">Pharmacology/Toxicology</JournalSubject><JournalSubject Type="Secondary">Pharmacy</JournalSubject><SubjectCollection Code="Medicine">SC11</SubjectCollection></JournalSubjectGroup></JournalInfo><Volume OutputMedium="All"><VolumeInfo TocLevels="0" VolumeType="Regular"><VolumeIDStart>35</VolumeIDStart><VolumeIDEnd>35</VolumeIDEnd><VolumeIssueCount>12</VolumeIssueCount></VolumeInfo><Issue IssueType="Regular" OutputMedium="All"><IssueInfo IssueType="Regular" TocLevels="0"><IssueIDStart>8</IssueIDStart><IssueIDEnd>8</IssueIDEnd><IssueArticleCount>21</IssueArticleCount><IssueHistory><OnlineDate><Year>2012</Year><Month>9</Month><Day>1</Day></OnlineDate><CoverDate><Year>2012</Year><Month>8</Month></CoverDate><PricelistYear>2012</PricelistYear></IssueHistory><IssueCopyright><CopyrightHolderName>The Pharmaceutical Society of Korea and Springer Netherlands</CopyrightHolderName><CopyrightYear>2012</CopyrightYear></IssueCopyright></IssueInfo><Article ID="s12272-012-0804-5" OutputMedium="All"><ArticleInfo ArticleType="OriginalPaper" ContainsESM="No" Language="En" NumberingStyle="Unnumbered" TocLevels="0"><ArticleID>804</ArticleID><ArticleDOI>10.1007/s12272-012-0804-5</ArticleDOI><ArticleSequenceNumber>5</ArticleSequenceNumber><ArticleTitle Language="En">Antiviral activity of <Emphasis Type="Italic">Aloe hijazensis</Emphasis> against some haemagglutinating viruses infection and its phytoconstituents</ArticleTitle><ArticleFirstPage>1347</ArticleFirstPage><ArticleLastPage>1354</ArticleLastPage><ArticleHistory><RegistrationDate><Year>2012</Year><Month>8</Month><Day>30</Day></RegistrationDate><Received><Year>2011</Year><Month>8</Month><Day>26</Day></Received><Revised><Year>2011</Year><Month>11</Month><Day>16</Day></Revised><Accepted><Year>2011</Year><Month>11</Month><Day>22</Day></Accepted><OnlineDate><Year>2012</Year><Month>9</Month><Day>1</Day></OnlineDate></ArticleHistory><ArticleCopyright><CopyrightHolderName>The Pharmaceutical Society of Korea and Springer Netherlands</CopyrightHolderName><CopyrightYear>2012</CopyrightYear></ArticleCopyright><ArticleGrants Type="Regular"><MetadataGrant Grant="OpenAccess"></MetadataGrant><AbstractGrant Grant="OpenAccess"></AbstractGrant><BodyPDFGrant Grant="Restricted"></BodyPDFGrant><BodyHTMLGrant Grant="Restricted"></BodyHTMLGrant><BibliographyGrant Grant="Restricted"></BibliographyGrant><ESMGrant Grant="Restricted"></ESMGrant></ArticleGrants></ArticleInfo><ArticleHeader><AuthorGroup><Author AffiliationIDS="Aff1" CorrespondingAffiliationID="Aff1"><AuthorName DisplayOrder="Western"><GivenName>Howaida</GivenName><GivenName>I.</GivenName><FamilyName>Abd-Alla</FamilyName></AuthorName><Contact><Fax>2-02-3337-0931</Fax><Email>howaida_nrc@yahoo.com</Email></Contact></Author><Author AffiliationIDS="Aff2"><AuthorName DisplayOrder="Western"><GivenName>Nagat</GivenName><GivenName>S.</GivenName><FamilyName>Abu-Gabal</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff1"><AuthorName DisplayOrder="Western"><GivenName>Amal</GivenName><GivenName>Z.</GivenName><FamilyName>Hassan</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff3"><AuthorName DisplayOrder="Western"><GivenName>Mounir</GivenName><GivenName>M.</GivenName><FamilyName>El-Safty</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff2"><AuthorName DisplayOrder="Western"><GivenName>Nagwa</GivenName><GivenName>M.</GivenName><GivenName>M.</GivenName><FamilyName>Shalaby</FamilyName></AuthorName></Author><Affiliation ID="Aff1"><OrgDivision>Department of Natural Compounds Chemistry</OrgDivision><OrgName>National Research Centre</OrgName><OrgAddress><City>Dokki</City><Postcode>12622</Postcode><Country Code="EG">Giza, Egypt</Country></OrgAddress></Affiliation><Affiliation ID="Aff2"><OrgDivision>Faculty of Science, Branch of Girls</OrgDivision><OrgName>King Abdul-Aziz University</OrgName><OrgAddress><City>Jeddah</City><Country Code="SA">Saudi Arabia</Country></OrgAddress></Affiliation><Affiliation ID="Aff3"><OrgName>Central Laboratory for Evaluation of Veterinary Biologics</OrgName><OrgAddress><City>Abbassia</City><Postcode>13181</Postcode><Country Code="EG">Cairo, Egypt</Country></OrgAddress></Affiliation></AuthorGroup><Abstract ID="Abs1" Language="En"><Heading>Abstract</Heading><Para>Evaluation of the antiviral activities of flowers, flower-peduncles, leaves, and roots of <Emphasis Type="Italic">Aloe hijazensis</Emphasis> against haemagglutinating viruses of avian paramyxovirus type-1 (APMV-1), avian influenza virus type A (AI-H5N1), Newcastle disease virus (NDV), and egg-drop syndrome virus (EDSV) in specific pathogen free (SPF) chicken embryos were carried out. Extract of the flowers and leaves showed relatively higher activity than the extracts of other plant parts. Thirteen compounds were isolated from both the flowers and flower-peduncles of <Emphasis Type="Italic">A. hijazensis</Emphasis>. The isolated compounds were classified into: five anthraquinones; ziganein, ziganein-5-methyl ether, aloesaponarin I, chrysophanol, aloe-emodin, one dihydroisocoumarin; feralolide, four flavonoids; homoplantaginin, isoorientin, luteolin 7-glucuronopyranoside, isovitexin, one phenolic acid; <Emphasis Type="Italic">p</Emphasis>-coumaric acid, the anthrone; barbaloin together with aloenin. Eleven compounds were attributed to the flowers and seven to the flower-peduncles. Homoplantaginin and luteolin 7-glucuronopyranoside are reported here for the first time from <Emphasis Type="Italic">Aloe</Emphasis> spp. To the best of our knowledge, this is the first report on the chemical composition and biological activity of those plant parts.</Para></Abstract><KeywordGroup Language="En"><Heading>Key words</Heading><Keyword><Emphasis Type="Italic">Aloe hijazensis</Emphasis></Keyword><Keyword>Haemagglutinating viruses</Keyword><Keyword>Phytochemical constituents</Keyword></KeywordGroup></ArticleHeader><NoBody></NoBody></Article></Issue></Volume></Journal></Publisher></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Antiviral activity of Aloe hijazensis against some haemagglutinating viruses infection and its phytoconstituents</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Antiviral activity of Aloe hijazensis against some haemagglutinating viruses infection and its phytoconstituents</title></titleInfo><name type="personal" displayLabel="corresp"><namePart type="given">Howaida</namePart><namePart type="given">I.</namePart><namePart type="family">Abd-Alla</namePart><affiliation>Department of Natural Compounds Chemistry, National Research Centre, 12622, Dokki, Giza, Egypt</affiliation><affiliation>E-mail: howaida_nrc@yahoo.com</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Nagat</namePart><namePart type="given">S.</namePart><namePart type="family">Abu-Gabal</namePart><affiliation>Faculty of Science, Branch of Girls, King Abdul-Aziz University, Jeddah, Saudi Arabia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Amal</namePart><namePart type="given">Z.</namePart><namePart type="family">Hassan</namePart><affiliation>Department of Natural Compounds Chemistry, National Research Centre, 12622, Dokki, Giza, Egypt</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Mounir</namePart><namePart type="given">M.</namePart><namePart type="family">El-Safty</namePart><affiliation>Central Laboratory for Evaluation of Veterinary Biologics, 13181, Abbassia, Cairo, Egypt</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Nagwa</namePart><namePart type="given">M.</namePart><namePart type="given">M.</namePart><namePart type="family">Shalaby</namePart><affiliation>Faculty of Science, Branch of Girls, King Abdul-Aziz University, Jeddah, Saudi Arabia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="OriginalPaper" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>Pharmaceutical Society of Korea</publisher><place><placeTerm type="text">Heidelberg</placeTerm></place><dateCreated encoding="w3cdtf">2011-08-26</dateCreated><dateIssued encoding="w3cdtf">2012-08-01</dateIssued><copyrightDate encoding="w3cdtf">2012</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><abstract lang="en">Abstract: Evaluation of the antiviral activities of flowers, flower-peduncles, leaves, and roots of Aloe hijazensis against haemagglutinating viruses of avian paramyxovirus type-1 (APMV-1), avian influenza virus type A (AI-H5N1), Newcastle disease virus (NDV), and egg-drop syndrome virus (EDSV) in specific pathogen free (SPF) chicken embryos were carried out. Extract of the flowers and leaves showed relatively higher activity than the extracts of other plant parts. Thirteen compounds were isolated from both the flowers and flower-peduncles of A. hijazensis. The isolated compounds were classified into: five anthraquinones; ziganein, ziganein-5-methyl ether, aloesaponarin I, chrysophanol, aloe-emodin, one dihydroisocoumarin; feralolide, four flavonoids; homoplantaginin, isoorientin, luteolin 7-glucuronopyranoside, isovitexin, one phenolic acid; p-coumaric acid, the anthrone; barbaloin together with aloenin. Eleven compounds were attributed to the flowers and seven to the flower-peduncles. Homoplantaginin and luteolin 7-glucuronopyranoside are reported here for the first time from Aloe spp. To the best of our knowledge, this is the first report on the chemical composition and biological activity of those plant parts.</abstract><subject lang="en"><genre>Key words</genre><topic>Aloe hijazensis</topic><topic>Haemagglutinating viruses</topic><topic>Phytochemical constituents</topic></subject><relatedItem type="host"><titleInfo><title>Archives of Pharmacal Research</title></titleInfo><titleInfo type="abbreviated"><title>Arch. Pharm. Res.</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><originInfo><publisher>Springer</publisher><dateIssued encoding="w3cdtf">2012-09-01</dateIssued><copyrightDate encoding="w3cdtf">2012</copyrightDate></originInfo><subject><genre>Journal-Subject-Collection</genre><topic authority="SpringerSubjectCodes" authorityURI="Medicine">SC11</topic></subject><subject><genre>Pharmacy</genre><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic></subject><identifier type="ISSN">0253-6269</identifier><identifier type="eISSN">1976-3786</identifier><identifier type="JournalID">12272</identifier><identifier type="IssueArticleCount">21</identifier><identifier type="VolumeIssueCount">12</identifier><part><date>2012</date><detail type="volume"><number>35</number><caption>vol.</caption></detail><detail type="issue"><number>8</number><caption>no.</caption></detail><extent unit="pages"><start>1347</start><end>1354</end></extent></part><recordInfo><recordOrigin>The Pharmaceutical Society of Korea and Springer Netherlands, 2012</recordOrigin></recordInfo></relatedItem><identifier type="istex">A424EB56D8AC34C4C6C1912296D02B2BC07554AC</identifier><identifier type="ark">ark:/67375/VQC-0RQK9GTV-B</identifier><identifier type="DOI">10.1007/s12272-012-0804-5</identifier><identifier type="ArticleID">804</identifier><identifier type="ArticleID">s12272-012-0804-5</identifier><accessCondition type="use and reproduction" contentType="copyright">The Pharmaceutical Society of Korea and Springer Netherlands, 2012</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-3XSW68JL-F">springer</recordContentSource><recordOrigin>The Pharmaceutical Society of Korea and Springer Netherlands, 2012</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/VQC-0RQK9GTV-B/record.json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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