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Medicinal plants from brazilian cerrado biome: Potential sources of new anti-inflammatory compounds and antitumor agents on ehrlich carcinoma

dc.contributor.authorMalara, Fábio de Andrade [UNESP]
dc.contributor.authorMatos, Djamile C. [UNESP]
dc.contributor.authorRibeiro, Lívia C.A. [UNESP]
dc.contributor.authorFalcoski, Thais O.R. [UNESP]
dc.contributor.authorAndrade, Teresinha J.A.S. [UNESP]
dc.contributor.authorSantos, Vanessa N.C.
dc.contributor.authorLima, Nerilson M.
dc.contributor.authorCarlos, Iracilda Z. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionInstituto de Ciências Biológicas/ICB
dc.contributor.institutionInstituto de Ciências Exatas/ICE
dc.date.accessioned2022-04-28T19:46:35Z
dc.date.available2022-04-28T19:46:35Z
dc.date.issued2021-01-01
dc.description.abstractThis work describes a pharmacological screening of Brazilian medicinal plants through their anti-inflammatory and cytotoxicity activities. Cytotoxicity activity of Mouriri elliptica and Alchornea glandulosa as well as the drugs celecoxib and doxorubicin were evaluated in cultures of peritoneal macrophages. The immune system influence of these samples was analyzed by determining production/inhibition of NO, production of tumor necrosis factor-α and production of interleukin-10. Regarding the production/inhibition of NO, there was NO production by M. elliptica and NO inhibition when the cells were exposed to A. glandulosa; Macrophages generally produce more NO, plus TNF-α and less IL-10, when associated to the tumor phenomenon, characterizing the inflammation involved in cancer. A. glandulosa showed anti-inflammatory effect, inhibited NO production and it was associated with low TNF-α production, although not as low as the macrophages associated with celecoxib and doxorubicin. These cytokines were not different in animals with tumor. Celecoxib confirms its anti-inflammatory action by markedly inhibiting NO and TNF-α, but also inhibiting IL-10 which is an anti-inflammatory cytokine. Doxorubicin inhibited NO in a higher percentage in the group of animals with tumor, although the literature reports that this drug stimulates the production of NO and this collaborates with its cytotoxic effect.en
dc.description.affiliationUniversidade Estadual Paulista “Júlio de Mesquita Filho”/ UNESP Faculdade de Ciências Farmacêuticas, Rod. Araraquara-Jaú Km 1, Machados
dc.description.affiliationUniversidade Federal do Amazonas/UFAM Instituto de Ciências Biológicas/ICB, Av. General Rodrigo Octavio Jordão Ramos, 1200, Coroado I
dc.description.affiliationUniversidade Federal de Juiz de Fora/UFJF Instituto de Ciências Exatas/ICE, Rua José Lourenço Kelmer, s/n, São Pedro
dc.description.affiliationUnespUniversidade Estadual Paulista “Júlio de Mesquita Filho”/ UNESP Faculdade de Ciências Farmacêuticas, Rod. Araraquara-Jaú Km 1, Machados
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.identifierhttp://dx.doi.org/10.1590/0001-3765202120191101
dc.identifier.citationAnais da Academia Brasileira de Ciencias, v. 93.
dc.identifier.doi10.1590/0001-3765202120191101
dc.identifier.issn1678-2690
dc.identifier.issn0001-3765
dc.identifier.scopus2-s2.0-85118256668
dc.identifier.urihttp://hdl.handle.net/11449/222764
dc.language.isoeng
dc.relation.ispartofAnais da Academia Brasileira de Ciencias
dc.sourceScopus
dc.subjectAlchornea glandulosa
dc.subjectAnti-inflammatory
dc.subjectCytotoxicity
dc.subjectEhrlich carcinoma
dc.subjectMouriri elliptica
dc.titleMedicinal plants from brazilian cerrado biome: Potential sources of new anti-inflammatory compounds and antitumor agents on ehrlich carcinomaen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.orcid0000-0003-3933-8992[1]
unesp.author.orcid0000-0002-5028-1301[2]
unesp.author.orcid0000-0003-0826-4599[3]
unesp.author.orcid0000-0002-3801-2811[4]
unesp.author.orcid0000-0002-2415-9222[5]
unesp.author.orcid0000-0003-1092-9334[6]
unesp.author.orcid0000-0001-9669-0306[7]
unesp.author.orcid0000-0002-0084-3468[8]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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