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 | Acesso ao texto completo restrito à biblioteca da Embrapa Gado de Leite. Para informações adicionais entre em contato com cnpgl.biblioteca@embrapa.br. |
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Registro Completo |
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Biblioteca(s): |
Embrapa Gado de Leite. |
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Data corrente: |
14/03/2013 |
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Data da última atualização: |
09/02/2024 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
MAZZOCCOLI, L.; CARDOSO, SILVIA H.; AMARANTE, G. W.; SOUZA, M. V. N. DE; DOMINGUES, R.; MACHADO, M. A.; ALMEIDA, M. V. DE; TEIXEIRA, H. C. |
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Afiliação: |
LUCIANO MAZZOCCOLI, UFJF; SILVIA H. CARDOSO, UFJF; GIOVANNI W. AMARANTE, UFJF; MARCUS V. N. DE SOUZA, UFJF; ROBERT DOMINGUES, CPPSUL; MARCO ANTONIO MACHADO, CNPGL; MAURO V. DE ALMEIDA, UFJF; HENRIQUE C. TEIXEIRA, UFJF. |
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Título: |
Novel thalidomide analogues from diamines inhibit pro-inflammatory cytokine production and CD80 expression while enhancing IL-10. |
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Ano de publicação: |
2012 |
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Fonte/Imprenta: |
Biomedicine & Pharmacotherapy, v. 66, p. 323-329, 2012. |
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DOI: |
https://doi.org/10.1016/j.biopha.2012.05.001 |
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Idioma: |
Inglês |
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Notas: |
Não consta da meta de 2012. |
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Conteúdo: |
Thalidomide is used to treat a variety of diseases including erythema nodosum leprosum, an inflammatory complication of leprosy. However, this drug has severe teratogenic activity and novel thalidomide analogues might be used to treat diseases without this severe side effect. A series of diamine compounds containing two hydrolyzed phthalimide units were chosen as analogues of thalidomide and evaluated regarding their capacity to regulate the production of molecules involved in inflammatory responses. TNF-α, IL-12 and IL-10 production, and the expression of CD80 and CD86 were investigated in LPS plus IFN-γ-stimulated J774A.1 cells by ELISA and flow cytometry, respectively. The expression of TNF-α and IL-10 mRNA was analyzed by real time RT-PCR. TNF-α, IL-6, IFN-γ, CXCL9 and CXCL10 production by human peripheral blood mononuclear cells (PBMC) were evaluated by flow cytometry. Compounds 3, 6 and 9 greatly inhibited TNF-α and IL-12 production while enhancing IL-10. In addition, CD80 expression was inhibited, but not CD86. The compounds inhibited TNF-α production by PBMC more than thalidomide and also had an inhibitory effect on the production of IL-6, IFN-γ, CXCL9 and CXCL10. Levels of mRNA for TNF-α were reduced after treatment with the compounds, suggesting post- transcriptional effects. The compounds had no effect on cell viability. Our results indicate that the novel diamine compounds 3, 6 and 9 inhibit critical pro-inflammatory cytokines and stimulate IL-10, which make them attractive candidate drugs for the treatment of certain inflammatory conditions and cancer. MenosThalidomide is used to treat a variety of diseases including erythema nodosum leprosum, an inflammatory complication of leprosy. However, this drug has severe teratogenic activity and novel thalidomide analogues might be used to treat diseases without this severe side effect. A series of diamine compounds containing two hydrolyzed phthalimide units were chosen as analogues of thalidomide and evaluated regarding their capacity to regulate the production of molecules involved in inflammatory responses. TNF-α, IL-12 and IL-10 production, and the expression of CD80 and CD86 were investigated in LPS plus IFN-γ-stimulated J774A.1 cells by ELISA and flow cytometry, respectively. The expression of TNF-α and IL-10 mRNA was analyzed by real time RT-PCR. TNF-α, IL-6, IFN-γ, CXCL9 and CXCL10 production by human peripheral blood mononuclear cells (PBMC) were evaluated by flow cytometry. Compounds 3, 6 and 9 greatly inhibited TNF-α and IL-12 production while enhancing IL-10. In addition, CD80 expression was inhibited, but not CD86. The compounds inhibited TNF-α production by PBMC more than thalidomide and also had an inhibitory effect on the production of IL-6, IFN-γ, CXCL9 and CXCL10. Levels of mRNA for TNF-α were reduced after treatment with the compounds, suggesting post- transcriptional effects. The compounds had no effect on cell viability. Our results indicate that the novel diamine compounds 3, 6 and 9 inhibit critical pro-inflammatory cytokines and stimulate IL-10, which make them... Mostrar Tudo |
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Palavras-Chave: |
IL-10; Resposta inflamatória; Talidomida analógico; TNF-a. |
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Categoria do assunto: |
H Saúde e Patologia |
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Marc: |
LEADER 02493naa a2200277 a 4500
001 1953088
005 2024-02-09
008 2012 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.1016/j.biopha.2012.05.001$2DOI
100 1 $aMAZZOCCOLI, L.
245 $aNovel thalidomide analogues from diamines inhibit pro-inflammatory cytokine production and CD80 expression while enhancing IL-10.$h[electronic resource]
260 $c2012
500 $aNão consta da meta de 2012.
520 $aThalidomide is used to treat a variety of diseases including erythema nodosum leprosum, an inflammatory complication of leprosy. However, this drug has severe teratogenic activity and novel thalidomide analogues might be used to treat diseases without this severe side effect. A series of diamine compounds containing two hydrolyzed phthalimide units were chosen as analogues of thalidomide and evaluated regarding their capacity to regulate the production of molecules involved in inflammatory responses. TNF-α, IL-12 and IL-10 production, and the expression of CD80 and CD86 were investigated in LPS plus IFN-γ-stimulated J774A.1 cells by ELISA and flow cytometry, respectively. The expression of TNF-α and IL-10 mRNA was analyzed by real time RT-PCR. TNF-α, IL-6, IFN-γ, CXCL9 and CXCL10 production by human peripheral blood mononuclear cells (PBMC) were evaluated by flow cytometry. Compounds 3, 6 and 9 greatly inhibited TNF-α and IL-12 production while enhancing IL-10. In addition, CD80 expression was inhibited, but not CD86. The compounds inhibited TNF-α production by PBMC more than thalidomide and also had an inhibitory effect on the production of IL-6, IFN-γ, CXCL9 and CXCL10. Levels of mRNA for TNF-α were reduced after treatment with the compounds, suggesting post- transcriptional effects. The compounds had no effect on cell viability. Our results indicate that the novel diamine compounds 3, 6 and 9 inhibit critical pro-inflammatory cytokines and stimulate IL-10, which make them attractive candidate drugs for the treatment of certain inflammatory conditions and cancer.
653 $aIL-10
653 $aResposta inflamatória
653 $aTalidomida analógico
653 $aTNF-a
700 1 $aCARDOSO, SILVIA H.
700 1 $aAMARANTE, G. W.
700 1 $aSOUZA, M. V. N. DE
700 1 $aDOMINGUES, R.
700 1 $aMACHADO, M. A.
700 1 $aALMEIDA, M. V. DE
700 1 $aTEIXEIRA, H. C.
773 $tBiomedicine & Pharmacotherapy$gv. 66, p. 323-329, 2012.
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Registro original: |
Embrapa Gado de Leite (CNPGL) |
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Classificação |
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Registro |
Volume |
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URL |
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Registro Completo
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Biblioteca(s): |
Embrapa Amapá; Embrapa Meio Ambiente; Embrapa Pesca e Aquicultura; Embrapa Roraima; Embrapa Tabuleiros Costeiros. |
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Data corrente: |
23/02/2017 |
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Data da última atualização: |
06/03/2017 |
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Tipo da produção científica: |
Documentos |
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Autoria: |
PEREIRA, S. L. A.; CHAGAS, E. C.; MACIEL, P. O.; BENAVIDES, M. V.; MAJOLO, C.; BOIJINK, C. de L.; TAVARES-DIAS, M.; ISHIKAWA, M. M.; FUJIMOTO, R. Y.; BRANDÃO, F. R.; SOUSA, K. L. de; MORAIS, M. da S.; MARTINS, V. F. da S. |
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Afiliação: |
SANDRO LORIS AQUINO PEREIRA, CPAF-Roraima; EDSANDRA CAMPOS CHAGAS, CPAA; PATRICIA OLIVEIRA MACIEL, CNPASA; MAGDA VIEIRA BENAVIDES, CPPSUL; CLAUDIA MAJOLO, CPAA; CHEILA DE LIMA BOIJINK, CPAA; MARCOS TAVARES DIAS, CPAF-AP; MARCIA MAYUMI ISHIKAWA, CNPMA; RODRIGO YUDI FUJIMOTO, CPATC; Franmir Rodrigues Brandão, Biólogo, doutorando no Programa Ciências Pesqueiras nos Trópicos (Cipet), UFAM; Kátia Lima de Sousa, Bióloga; Mayene da Silva Morais, Bióloga; Valéria Fernanda da Silva Martins, Bióloga. |
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Título: |
Agentes patogênicos de tambaquis cultivados, com destaque para registros em Rio Preto da Eva, AM. |
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Ano de publicação: |
2016 |
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Fonte/Imprenta: |
Manaus: Embrapa Amazônia Ocidental, 2016. |
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Páginas: |
80 p. |
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Série: |
(Embrapa Amazônia Ocidental. Documentos, 127). |
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ISSN: |
1517-3135 |
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Idioma: |
Português |
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Conteúdo: |
Parasitos registrados na criação de tambaqui. Parasitos protozoários. Ichthyophthirius multifiliis. Agente etiológico. Sinais nos peixes parasitados. Condições de desenvolvimento. Manejo sanitário e recomendações. Trichodina spp. Piscinoodinium pillulare. Tetrahymena spp. Mixosporídeos. Monogenea. Digenea. Nematoda. Acantocéfalos. Crustáceos. Branquiúros. Copepoda. Isopoda. Bacterioses registradas na criação de tambaqui. Aeromonas hydrophila. Flavobacterium columnare. Streptococcus sp. Lactococcus. Edwardsiella tarda. Boas práticas de manejo sanitário. |
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Thesagro: |
Peixe de Água Doce; Sanidade Animal; Tambaqui. |
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Categoria do assunto: |
--
H Saúde e Patologia
L Ciência Animal e Produtos de Origem Animal
S Ciências Biológicas |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/156602/1/Doc-127-fechado.pdf
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Marc: |
LEADER 01534nam a2200325 a 4500
001 2066259
005 2017-03-06
008 2016 bl uuuu u0uu1 u #d
022 $a1517-3135
100 1 $aPEREIRA, S. L. A.
245 $aAgentes patogênicos de tambaquis cultivados, com destaque para registros em Rio Preto da Eva, AM.$h[electronic resource]
260 $aManaus: Embrapa Amazônia Ocidental$c2016
300 $a80 p.
490 $a(Embrapa Amazônia Ocidental. Documentos, 127).
520 $aParasitos registrados na criação de tambaqui. Parasitos protozoários. Ichthyophthirius multifiliis. Agente etiológico. Sinais nos peixes parasitados. Condições de desenvolvimento. Manejo sanitário e recomendações. Trichodina spp. Piscinoodinium pillulare. Tetrahymena spp. Mixosporídeos. Monogenea. Digenea. Nematoda. Acantocéfalos. Crustáceos. Branquiúros. Copepoda. Isopoda. Bacterioses registradas na criação de tambaqui. Aeromonas hydrophila. Flavobacterium columnare. Streptococcus sp. Lactococcus. Edwardsiella tarda. Boas práticas de manejo sanitário.
650 $aPeixe de Água Doce
650 $aSanidade Animal
650 $aTambaqui
700 1 $aCHAGAS, E. C.
700 1 $aMACIEL, P. O.
700 1 $aBENAVIDES, M. V.
700 1 $aMAJOLO, C.
700 1 $aBOIJINK, C. de L.
700 1 $aTAVARES-DIAS, M.
700 1 $aISHIKAWA, M. M.
700 1 $aFUJIMOTO, R. Y.
700 1 $aBRANDÃO, F. R.
700 1 $aSOUSA, K. L. de
700 1 $aMORAIS, M. da S.
700 1 $aMARTINS, V. F. da S.
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Embrapa Pesca e Aquicultura (CNPASA) |
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