DC FieldValueLanguage
dc.contributor.authorda Silva Napoleão, Sarah Maria-
dc.contributor.authorBernardes, João Paulo Romualdo Alarcão-
dc.contributor.authorTenório, Bernardo Guerra-
dc.contributor.authorMoreno Cardenas, Calisto-
dc.contributor.authorDallago, Bruno Stéfano Lima-
dc.contributor.authorÇiçek, Serhat Sezai-
dc.contributor.authorBezerra, Roberto Messias-
dc.contributor.authorSegovia, Jorge Federico Orellana-
dc.contributor.authorGomes da Mata Kanzaki, Elida Cleyse-
dc.contributor.authorKanzaki, Isamu-
dc.date.accessioned2026-02-09T16:10:23Z-
dc.date.available2026-02-09T16:10:23Z-
dc.date.issued2024-12-03-
dc.identifier.urihttps://hdl.handle.net/20.500.12738/18667-
dc.description.abstractBackground Novel antiretroviral drugs are in constant need for HIV/AIDS patients to face the continuous emerging resistance to the commonly prescribed combination of anti-HIV synthetic agents and their side effects. Methods Amazonian medicinal plants, Licania macrophylla (Chrysobalanaceae) and Ouratea hexasperma (Ochnaceae) were assayed for antiretroviral and immunomodulatory activity, utilizing an established human leukocyte cell line and the Simian Immunodeficiency Virus. The IL-4, IL-6, IL-8, IL-10 and IFN-y cytokines were quantified after leukocyte culture stimulation with ethanolic plant extracts and challenged with lentivirus infection. Results Mitotic activity induced by O. hexasperma extract was significatively more pronounced than L. macrophylla extract. Cytokine modulation was recorded in SIV infected cells under independent treatment with O. hexasperma and L. macrophylla extracts. Betulinic acid, ninuriflavone, (-)epigallocathechine, (-)gallocatechine and 4-O-methyl-epigallocatechin were isolated from L. macrophyla. Conclusions Cellular proliferative activity and cytokine modulation by the extracts assayed have potential applications in the therapy of HIV/AIDS pathology, as the isolated compounds of these plants have been reported for antiviral activity.en
dc.language.isoenen_US
dc.publisherCold Spring Harbor Laboratoryen_US
dc.relation.ispartofbioRxiv betaen_US
dc.subject.ddc610: Medizinen_US
dc.titlePotential antiviral and immunomodulatory Amazonian medicinal plant compoundsen
dc.typePreprinten_US
dc.description.versionReviewPendingen_US
openaire.rightsinfo:eu-repo/semantics/openAccessen_US
tuhh.identifier.urnurn:nbn:de:gbv:18302-reposit-228178-
tuhh.oai.showtrueen_US
tuhh.publication.instituteFakultät Life Sciences (ehemalig, aufgelöst 10.2025)en_US
tuhh.publication.instituteDepartment Biotechnologie (ehemalig, aufgelöst 10.2025)en_US
tuhh.publisher.doi10.1101/2024.11.27.625749-
tuhh.type.opusPreprint (Vorabdruck)-
dc.rights.cchttps://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.type.casraiOther-
dc.type.dinipreprint-
dc.type.driverpreprint-
dc.type.statusinfo:eu-repo/semantics/publishedVersionen_US
dcterms.DCMITypeText-
datacite.relation.IsPreviousVersionOfdoi:10.36922/mi.8367-
datacite.relation.IsPreviousVersionOfhdl:20.500.12738/17335-
tuhh.apc.statusfalseen_US
item.creatorOrcidda Silva Napoleão, Sarah Maria-
item.creatorOrcidBernardes, João Paulo Romualdo Alarcão-
item.creatorOrcidTenório, Bernardo Guerra-
item.creatorOrcidMoreno Cardenas, Calisto-
item.creatorOrcidDallago, Bruno Stéfano Lima-
item.creatorOrcidÇiçek, Serhat Sezai-
item.creatorOrcidBezerra, Roberto Messias-
item.creatorOrcidSegovia, Jorge Federico Orellana-
item.creatorOrcidGomes da Mata Kanzaki, Elida Cleyse-
item.creatorOrcidKanzaki, Isamu-
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.creatorGNDda Silva Napoleão, Sarah Maria-
item.creatorGNDBernardes, João Paulo Romualdo Alarcão-
item.creatorGNDTenório, Bernardo Guerra-
item.creatorGNDMoreno Cardenas, Calisto-
item.creatorGNDDallago, Bruno Stéfano Lima-
item.creatorGNDÇiçek, Serhat Sezai-
item.creatorGNDBezerra, Roberto Messias-
item.creatorGNDSegovia, Jorge Federico Orellana-
item.creatorGNDGomes da Mata Kanzaki, Elida Cleyse-
item.creatorGNDKanzaki, Isamu-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_816b-
item.cerifentitytypePublications-
item.openairetypePreprint-
crisitem.author.deptDepartment Biotechnologie (ehemalig, aufgelöst 10.2025)-
crisitem.author.orcid0000-0002-3038-8523-
crisitem.author.parentorgFakultät Life Sciences (ehemalig, aufgelöst 10.2025)-
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