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Inhibition of nitric oxide and tumour necrosis factor-α production in peritoneal macrophages by aspergillus nidulans melanin

dc.contributor.authorDe Cassia Ribeiro Goncalves, Rita
dc.contributor.authorKitagawa, Rodrigo Rezende
dc.contributor.authorRaddi, Maria Stella Gonçalves [UNESP]
dc.contributor.authorCarlos, Iracilda Zeppone [UNESP]
dc.contributor.authorPombeiro-Sponchiado, Sandra Regina [UNESP]
dc.contributor.institutionEspirito Santo Federal University-UFES
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2022-04-29T07:13:25Z
dc.date.available2022-04-29T07:13:25Z
dc.date.issued2013-12-01
dc.description.abstractThe naturally occurring pigment, melanin is found in organisms of all phylogenetic kingdoms, including fungi, and exhibits a wide range of biological activities. Our objective was to investigate the effects of melanin extracted from the fungus Aspergillus nidulans on the production of the pro-inflammatory mediators nitric oxide (NO) and tumour necrosis factor-α (TNF-α) in peritoneal macrophages and on the viability of McCoy mouse fibroblasts. The results showed that A. nidulans melanin did not stimulate NO production in macrophages, but it inhibited the NO production in lipopolysaccharide (LPS)-stimulated macrophages by approximately 82%. Similarly, A. nidulans melanin inhibited LPS-stimulated TNF-α production by 52% and showed a slight stimulatory effect on TNF-α production in macrophages. In addition, the toxicity of A. nidulans melanin to McCoy cells was much lesser (IC50373.5 -2.4 μg/mL) than that of known agents such as cisplatin (IC5041.2 μg/mL). The viability of peritoneal macrophages was greater than 90% at the highest melanin concentration tested (100 μg/mL). Thus, the combination of low cytotoxicity and marked inhibition of TNF-α and NO production suggests that A. nidulans melanin has potential as an anti-inflammatory agent and may be used in the future for development of new drugs with therapeutic utility. © 2013 The Pharmaceutical Society of Japan.en
dc.description.affiliationDepartament of Pharmaceutical Sciences Espirito Santo Federal University-UFES, Av. Marechal Campos 1488, Vitoria, ES CEP 29040-090
dc.description.affiliationDepartment of Clinical Analysis Faculty of Pharmaceutical Sciences São Paulo State University-UNESP, R. Expedicionários do Brasil 1601, CEP 14801-902, Araraquara, São Paulo
dc.description.affiliationDepartment of Biochemistry and Technology Chemistry Institute of Chemistry São Paulo State University-UNESP, R. Prof. Francisco Degni, 55, CP 355, Araraquara, SP CEP 14801-970
dc.description.affiliationUnespDepartment of Clinical Analysis Faculty of Pharmaceutical Sciences São Paulo State University-UNESP, R. Expedicionários do Brasil 1601, CEP 14801-902, Araraquara, São Paulo
dc.description.affiliationUnespDepartment of Biochemistry and Technology Chemistry Institute of Chemistry São Paulo State University-UNESP, R. Prof. Francisco Degni, 55, CP 355, Araraquara, SP CEP 14801-970
dc.format.extent1915-1920
dc.identifierhttp://dx.doi.org/10.1248/bpb.b13-00445
dc.identifier.citationBiological and Pharmaceutical Bulletin, v. 36, n. 12, p. 1915-1920, 2013.
dc.identifier.doi10.1248/bpb.b13-00445
dc.identifier.issn0918-6158
dc.identifier.issn1347-5215
dc.identifier.scopus2-s2.0-84892582604
dc.identifier.urihttp://hdl.handle.net/11449/227474
dc.language.isoeng
dc.relation.ispartofBiological and Pharmaceutical Bulletin
dc.sourceScopus
dc.subjectAspergillus nidulans
dc.subjectFungus
dc.subjectMelanin
dc.subjectNitric oxide
dc.subjectTumour necrosis factor-α
dc.titleInhibition of nitric oxide and tumour necrosis factor-α production in peritoneal macrophages by aspergillus nidulans melaninen
dc.typeArtigopt
dspace.entity.typePublication
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relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
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unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentAnálises Clínicas - FCFpt
unesp.departmentBioquímica e Tecnologia - IQpt

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