Inhibition of Nitric Oxide and Tumour Necrosis Factor-alpha Production in Peritoneal Macrophages by Aspergillus nidulans Melanin

Detalhes bibliográficos
Autor(a) principal: Ribeiro Goncalves, Rita de Cassia
Data de Publicação: 2013
Outros Autores: Kitagawa, Rodrigo Rezende, Goncalves Raddi, Maria Stella [UNESP], Carlos, Iracilda Zeppone [UNESP], Pombeiro-Sponchiado, Sandra Regina
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/11449/113439
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-alpha (TNF-alpha) 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-alpha production by 52% and showed a slight stimulatory effect on TNF-alpha production in macrophages. In addition, the toxicity of A. nidulans melanin to McCoy cells was much lesser (IC50=373.5 +/- 2.4 mu g/mL) than that of known agents such as cisplatin (IC50=41.2 mu g/mL). The viability of peritoneal macrophages was greater than 90% at the highest melanin concentration tested (100 mu g/mL). Thus, the combination of low cytotoxicity and marked inhibition of TNF-alpha 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.
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spelling Inhibition of Nitric Oxide and Tumour Necrosis Factor-alpha Production in Peritoneal Macrophages by Aspergillus nidulans MelaninAspergillus nidulansmelaninnitric oxidetumour necrosis factor-alphafungusThe 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-alpha (TNF-alpha) 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-alpha production by 52% and showed a slight stimulatory effect on TNF-alpha production in macrophages. In addition, the toxicity of A. nidulans melanin to McCoy cells was much lesser (IC50=373.5 +/- 2.4 mu g/mL) than that of known agents such as cisplatin (IC50=41.2 mu g/mL). The viability of peritoneal macrophages was greater than 90% at the highest melanin concentration tested (100 mu g/mL). Thus, the combination of low cytotoxicity and marked inhibition of TNF-alpha 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.Programa de Apoio a Pos-graduacao (PROAP-UNESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Univ Fed Espirito Santo, Dept Pharmaceut Sci, BR-29040090 Vitoria, ES, BrazilSao Paulo State Univ UNESP, Fac Pharmaceut Sci, Dept Clin Anal, BR-14801902 Araraquara, SP, BrazilSao Paulo State Univ UNESP, Inst Chem, Dept Biochem & Technol Chem, BR-14801970 Araraquara, SP, BrazilSao Paulo State Univ UNESP, Fac Pharmaceut Sci, Dept Clin Anal, BR-14801902 Araraquara, SP, BrazilSao Paulo State Univ UNESP, Inst Chem, Dept Biochem & Technol Chem, BR-14801970 Araraquara, SP, BrazilPharmaceutical Soc JapanUniversidade Federal do Espírito Santo (UFES)Universidade Estadual Paulista (Unesp)Ribeiro Goncalves, Rita de CassiaKitagawa, Rodrigo RezendeGoncalves Raddi, Maria Stella [UNESP]Carlos, Iracilda Zeppone [UNESP]Pombeiro-Sponchiado, Sandra Regina2014-12-03T13:11:42Z2014-12-03T13:11:42Z2013-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1915-1920application/pdfhttp://dx.doi.org/10.1248/bpb.b13-00445Biological & Pharmaceutical Bulletin. Tokyo: Pharmaceutical Soc Japan, v. 36, n. 12, p. 1915-1920, 2013.0918-6158http://hdl.handle.net/11449/113439WOS:000327573800006WOS000327573800006.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBiological & Pharmaceutical Bulletin1.6940,626info:eu-repo/semantics/openAccess2024-01-07T06:22:17Zoai:repositorio.unesp.br:11449/113439Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-01-07T06:22:17Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Inhibition of Nitric Oxide and Tumour Necrosis Factor-alpha Production in Peritoneal Macrophages by Aspergillus nidulans Melanin
title Inhibition of Nitric Oxide and Tumour Necrosis Factor-alpha Production in Peritoneal Macrophages by Aspergillus nidulans Melanin
spellingShingle Inhibition of Nitric Oxide and Tumour Necrosis Factor-alpha Production in Peritoneal Macrophages by Aspergillus nidulans Melanin
Ribeiro Goncalves, Rita de Cassia
Aspergillus nidulans
melanin
nitric oxide
tumour necrosis factor-alpha
fungus
title_short Inhibition of Nitric Oxide and Tumour Necrosis Factor-alpha Production in Peritoneal Macrophages by Aspergillus nidulans Melanin
title_full Inhibition of Nitric Oxide and Tumour Necrosis Factor-alpha Production in Peritoneal Macrophages by Aspergillus nidulans Melanin
title_fullStr Inhibition of Nitric Oxide and Tumour Necrosis Factor-alpha Production in Peritoneal Macrophages by Aspergillus nidulans Melanin
title_full_unstemmed Inhibition of Nitric Oxide and Tumour Necrosis Factor-alpha Production in Peritoneal Macrophages by Aspergillus nidulans Melanin
title_sort Inhibition of Nitric Oxide and Tumour Necrosis Factor-alpha Production in Peritoneal Macrophages by Aspergillus nidulans Melanin
author Ribeiro Goncalves, Rita de Cassia
author_facet Ribeiro Goncalves, Rita de Cassia
Kitagawa, Rodrigo Rezende
Goncalves Raddi, Maria Stella [UNESP]
Carlos, Iracilda Zeppone [UNESP]
Pombeiro-Sponchiado, Sandra Regina
author_role author
author2 Kitagawa, Rodrigo Rezende
Goncalves Raddi, Maria Stella [UNESP]
Carlos, Iracilda Zeppone [UNESP]
Pombeiro-Sponchiado, Sandra Regina
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal do Espírito Santo (UFES)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Ribeiro Goncalves, Rita de Cassia
Kitagawa, Rodrigo Rezende
Goncalves Raddi, Maria Stella [UNESP]
Carlos, Iracilda Zeppone [UNESP]
Pombeiro-Sponchiado, Sandra Regina
dc.subject.por.fl_str_mv Aspergillus nidulans
melanin
nitric oxide
tumour necrosis factor-alpha
fungus
topic Aspergillus nidulans
melanin
nitric oxide
tumour necrosis factor-alpha
fungus
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-alpha (TNF-alpha) 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-alpha production by 52% and showed a slight stimulatory effect on TNF-alpha production in macrophages. In addition, the toxicity of A. nidulans melanin to McCoy cells was much lesser (IC50=373.5 +/- 2.4 mu g/mL) than that of known agents such as cisplatin (IC50=41.2 mu g/mL). The viability of peritoneal macrophages was greater than 90% at the highest melanin concentration tested (100 mu g/mL). Thus, the combination of low cytotoxicity and marked inhibition of TNF-alpha 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.
publishDate 2013
dc.date.none.fl_str_mv 2013-12-01
2014-12-03T13:11:42Z
2014-12-03T13:11:42Z
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 & Pharmaceutical Bulletin. Tokyo: Pharmaceutical Soc Japan, v. 36, n. 12, p. 1915-1920, 2013.
0918-6158
http://hdl.handle.net/11449/113439
WOS:000327573800006
WOS000327573800006.pdf
url http://dx.doi.org/10.1248/bpb.b13-00445
http://hdl.handle.net/11449/113439
identifier_str_mv Biological & Pharmaceutical Bulletin. Tokyo: Pharmaceutical Soc Japan, v. 36, n. 12, p. 1915-1920, 2013.
0918-6158
WOS:000327573800006
WOS000327573800006.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biological & Pharmaceutical Bulletin
1.694
0,626
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1915-1920
application/pdf
dc.publisher.none.fl_str_mv Pharmaceutical Soc Japan
publisher.none.fl_str_mv Pharmaceutical Soc Japan
dc.source.none.fl_str_mv Web of Science
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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