Inhibition of nitric oxide and tumour necrosis factor-α production in peritoneal macrophages by aspergillus nidulans melanin
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , |
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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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 |
|
_version_ |
1808128271114567680 |