Publicação: Medicinal plants from brazilian cerrado biome: Potential sources of new anti-inflammatory compounds and antitumor agents on ehrlich carcinoma
dc.contributor.author | Malara, Fábio de Andrade [UNESP] | |
dc.contributor.author | Matos, Djamile C. [UNESP] | |
dc.contributor.author | Ribeiro, Lívia C.A. [UNESP] | |
dc.contributor.author | Falcoski, Thais O.R. [UNESP] | |
dc.contributor.author | Andrade, Teresinha J.A.S. [UNESP] | |
dc.contributor.author | Santos, Vanessa N.C. | |
dc.contributor.author | Lima, Nerilson M. | |
dc.contributor.author | Carlos, Iracilda Z. [UNESP] | |
dc.contributor.institution | Universidade Estadual Paulista (UNESP) | |
dc.contributor.institution | Instituto de Ciências Biológicas/ICB | |
dc.contributor.institution | Instituto de Ciências Exatas/ICE | |
dc.date.accessioned | 2022-04-28T19:46:35Z | |
dc.date.available | 2022-04-28T19:46:35Z | |
dc.date.issued | 2021-01-01 | |
dc.description.abstract | This 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.affiliation | Universidade Estadual Paulista “Júlio de Mesquita Filho”/ UNESP Faculdade de Ciências Farmacêuticas, Rod. Araraquara-Jaú Km 1, Machados | |
dc.description.affiliation | Universidade Federal do Amazonas/UFAM Instituto de Ciências Biológicas/ICB, Av. General Rodrigo Octavio Jordão Ramos, 1200, Coroado I | |
dc.description.affiliation | Universidade Federal de Juiz de Fora/UFJF Instituto de Ciências Exatas/ICE, Rua José Lourenço Kelmer, s/n, São Pedro | |
dc.description.affiliationUnesp | Universidade Estadual Paulista “Júlio de Mesquita Filho”/ UNESP Faculdade de Ciências Farmacêuticas, Rod. Araraquara-Jaú Km 1, Machados | |
dc.description.sponsorship | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) | |
dc.description.sponsorship | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.identifier | http://dx.doi.org/10.1590/0001-3765202120191101 | |
dc.identifier.citation | Anais da Academia Brasileira de Ciencias, v. 93. | |
dc.identifier.doi | 10.1590/0001-3765202120191101 | |
dc.identifier.issn | 1678-2690 | |
dc.identifier.issn | 0001-3765 | |
dc.identifier.scopus | 2-s2.0-85118256668 | |
dc.identifier.uri | http://hdl.handle.net/11449/222764 | |
dc.language.iso | eng | |
dc.relation.ispartof | Anais da Academia Brasileira de Ciencias | |
dc.source | Scopus | |
dc.subject | Alchornea glandulosa | |
dc.subject | Anti-inflammatory | |
dc.subject | Cytotoxicity | |
dc.subject | Ehrlich carcinoma | |
dc.subject | Mouriri elliptica | |
dc.title | Medicinal plants from brazilian cerrado biome: Potential sources of new anti-inflammatory compounds and antitumor agents on ehrlich carcinoma | en |
dc.type | Artigo | pt |
dspace.entity.type | Publication | |
relation.isOrgUnitOfPublication | 95697b0b-8977-4af6-88d5-c29c80b5ee92 | |
relation.isOrgUnitOfPublication.latestForDiscovery | 95697b0b-8977-4af6-88d5-c29c80b5ee92 | |
unesp.author.orcid | 0000-0003-3933-8992[1] | |
unesp.author.orcid | 0000-0002-5028-1301[2] | |
unesp.author.orcid | 0000-0003-0826-4599[3] | |
unesp.author.orcid | 0000-0002-3801-2811[4] | |
unesp.author.orcid | 0000-0002-2415-9222[5] | |
unesp.author.orcid | 0000-0003-1092-9334[6] | |
unesp.author.orcid | 0000-0001-9669-0306[7] | |
unesp.author.orcid | 0000-0002-0084-3468[8] | |
unesp.campus | Universidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquara | pt |