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

Detalhes bibliográficos
Autor(a) principal: De Cassia Ribeiro Goncalves, Rita
Data de Publicação: 2013
Outros Autores: Kitagawa, Rodrigo Rezende, Raddi, Maria Stella Gonçalves [UNESP], Carlos, Iracilda Zeppone [UNESP], Pombeiro-Sponchiado, Sandra Regina [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1248/bpb.b13-00445
http://hdl.handle.net/11449/227474
Resumo: The 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.
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spelling Inhibition of nitric oxide and tumour necrosis factor-α production in peritoneal macrophages by aspergillus nidulans melaninAspergillus nidulansFungusMelaninNitric oxideTumour necrosis factor-αThe 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.Departament of Pharmaceutical Sciences Espirito Santo Federal University-UFES, Av. Marechal Campos 1488, Vitoria, ES CEP 29040-090Department of Clinical Analysis Faculty of Pharmaceutical Sciences São Paulo State University-UNESP, R. Expedicionários do Brasil 1601, CEP 14801-902, Araraquara, São PauloDepartment of Biochemistry and Technology Chemistry Institute of Chemistry São Paulo State University-UNESP, R. Prof. Francisco Degni, 55, CP 355, Araraquara, SP CEP 14801-970Department of Clinical Analysis Faculty of Pharmaceutical Sciences São Paulo State University-UNESP, R. Expedicionários do Brasil 1601, CEP 14801-902, Araraquara, São PauloDepartment of Biochemistry and Technology Chemistry Institute of Chemistry São Paulo State University-UNESP, R. Prof. Francisco Degni, 55, CP 355, Araraquara, SP CEP 14801-970Espirito Santo Federal University-UFESUniversidade Estadual Paulista (UNESP)De Cassia Ribeiro Goncalves, RitaKitagawa, Rodrigo RezendeRaddi, Maria Stella Gonçalves [UNESP]Carlos, Iracilda Zeppone [UNESP]Pombeiro-Sponchiado, Sandra Regina [UNESP]2022-04-29T07:13:25Z2022-04-29T07:13:25Z2013-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1915-1920http://dx.doi.org/10.1248/bpb.b13-00445Biological and Pharmaceutical Bulletin, v. 36, n. 12, p. 1915-1920, 2013.0918-61581347-5215http://hdl.handle.net/11449/22747410.1248/bpb.b13-004452-s2.0-84892582604Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBiological and Pharmaceutical Bulletininfo:eu-repo/semantics/openAccess2024-06-21T15:18:08Zoai:repositorio.unesp.br:11449/227474Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T13:45:11.352200Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Inhibition of nitric oxide and tumour necrosis factor-α production in peritoneal macrophages by aspergillus nidulans melanin
title Inhibition of nitric oxide and tumour necrosis factor-α production in peritoneal macrophages by aspergillus nidulans melanin
spellingShingle Inhibition of nitric oxide and tumour necrosis factor-α production in peritoneal macrophages by aspergillus nidulans melanin
De Cassia Ribeiro Goncalves, Rita
Aspergillus nidulans
Fungus
Melanin
Nitric oxide
Tumour necrosis factor-α
title_short Inhibition of nitric oxide and tumour necrosis factor-α production in peritoneal macrophages by aspergillus nidulans melanin
title_full Inhibition of nitric oxide and tumour necrosis factor-α production in peritoneal macrophages by aspergillus nidulans melanin
title_fullStr Inhibition of nitric oxide and tumour necrosis factor-α production in peritoneal macrophages by aspergillus nidulans melanin
title_full_unstemmed Inhibition of nitric oxide and tumour necrosis factor-α production in peritoneal macrophages by aspergillus nidulans melanin
title_sort Inhibition of nitric oxide and tumour necrosis factor-α production in peritoneal macrophages by aspergillus nidulans melanin
author De Cassia Ribeiro Goncalves, Rita
author_facet De Cassia Ribeiro Goncalves, Rita
Kitagawa, Rodrigo Rezende
Raddi, Maria Stella Gonçalves [UNESP]
Carlos, Iracilda Zeppone [UNESP]
Pombeiro-Sponchiado, Sandra Regina [UNESP]
author_role author
author2 Kitagawa, Rodrigo Rezende
Raddi, Maria Stella Gonçalves [UNESP]
Carlos, Iracilda Zeppone [UNESP]
Pombeiro-Sponchiado, Sandra Regina [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Espirito Santo Federal University-UFES
Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv De Cassia Ribeiro Goncalves, Rita
Kitagawa, Rodrigo Rezende
Raddi, Maria Stella Gonçalves [UNESP]
Carlos, Iracilda Zeppone [UNESP]
Pombeiro-Sponchiado, Sandra Regina [UNESP]
dc.subject.por.fl_str_mv Aspergillus nidulans
Fungus
Melanin
Nitric oxide
Tumour necrosis factor-α
topic Aspergillus nidulans
Fungus
Melanin
Nitric oxide
Tumour necrosis factor-α
description The 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.
publishDate 2013
dc.date.none.fl_str_mv 2013-12-01
2022-04-29T07:13:25Z
2022-04-29T07:13:25Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1248/bpb.b13-00445
Biological and Pharmaceutical Bulletin, v. 36, n. 12, p. 1915-1920, 2013.
0918-6158
1347-5215
http://hdl.handle.net/11449/227474
10.1248/bpb.b13-00445
2-s2.0-84892582604
url http://dx.doi.org/10.1248/bpb.b13-00445
http://hdl.handle.net/11449/227474
identifier_str_mv Biological and Pharmaceutical Bulletin, v. 36, n. 12, p. 1915-1920, 2013.
0918-6158
1347-5215
10.1248/bpb.b13-00445
2-s2.0-84892582604
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biological and Pharmaceutical Bulletin
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1915-1920
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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