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Registro Completo |
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Biblioteca(s): |
Embrapa Amapá. |
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Data corrente: |
28/11/2021 |
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Data da última atualização: |
28/11/2021 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
COSTA, D. P. da; CASTILHO, C. de L.; SANTOS, U. R. A. dos; GEMAQUE, T. C.; DAMASCENO, L. F.; LIMA, J. de F.; MIRANDA FILHO, K. C. |
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Afiliação: |
DANIEL PEREIRA DA COSTA, UEAP; CLAUDIANA DE LIMA CASTILHO, UFRA; UCLÉDIA ROBERTA ALBERTO DOS SANTOS, UFSC; TAINÁRA CUNHA GEMAQUE, UFMG; LEANDRO FERNANDES DAMASCENO, CPAF-AP; JO DE FARIAS LIMA, CPAF-AP; KLEBER CAMPOS MIRANDA FILHO, UFMG. |
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Título: |
Effect of dietary carotenoids on reproducers of Amazon River prawn Macrobrachium amazonicum. Part 1: metabolism,morphometric / zootechnical indexes, body composition and gametes. |
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Ano de publicação: |
2021 |
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Fonte/Imprenta: |
Journal of Agricultural Studies, v. 9, n. 2, p. 32-56, 2021. |
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Idioma: |
Inglês |
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Conteúdo: |
The inclusion of natural extracts and solution of synthetic astaxan thin in the Macrobrachium amazonicum diet w ere tested to verify their effect on performance, body indexes and total accumulation of astaxanthin in the reproductive tissues and gametes of this crustacean in comparison with newly captured wild animals. The e xperi ment was randomized in blocks (five treatments with three replicates). Four groups were submitted, during 20 days, to diets in recirculation tanks: control diet (CONT); diet containing natural extract of “buriti” (CAR); diet with inclusion of natural “uruc um” extract (BIXN), diet with syntheti c astaxanthin (ASTX) and NATURAL group (not fed with ration). 180 prawns were used, with 60 males (6.08±1.96 g) and 120 females (4.55±1.03 g) distributed in five groups containing four males and eight females each . The re were no significant differences in performance and body indexes. The number of released spermatozoids, live spermatozoids, body and egg pigmentation was higher in BIXN and ASTX treatments. The ASTX treatment was superior to the NATURAL group in the body pigmentation of females and eggs and release of spermatophores by males. These results demonstrate that the use of natural and artificial carotenoid pigments in the diet are beneficial for reproduction of M. amazonicum. |
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Palavras-Chave: |
Electroejaculation; Prawn culture. |
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Thesagro: |
Buriti; Urucum. |
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Thesaurus Nal: |
Astaxanthin; Reproductive performance. |
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Categoria do assunto: |
S Ciências Biológicas |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/228190/1/CPAF-AP-2021-Effect-of-dietary-carotenoids-part-1.pdf
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Marc: |
LEADER 02205naa a2200265 a 4500
001 2136703
005 2021-11-28
008 2021 bl uuuu u00u1 u #d
100 1 $aCOSTA, D. P. da
245 $aEffect of dietary carotenoids on reproducers of Amazon River prawn Macrobrachium amazonicum. Part 1$bmetabolism,morphometric / zootechnical indexes, body composition and gametes.$h[electronic resource]
260 $c2021
520 $aThe inclusion of natural extracts and solution of synthetic astaxan thin in the Macrobrachium amazonicum diet w ere tested to verify their effect on performance, body indexes and total accumulation of astaxanthin in the reproductive tissues and gametes of this crustacean in comparison with newly captured wild animals. The e xperi ment was randomized in blocks (five treatments with three replicates). Four groups were submitted, during 20 days, to diets in recirculation tanks: control diet (CONT); diet containing natural extract of “buriti” (CAR); diet with inclusion of natural “uruc um” extract (BIXN), diet with syntheti c astaxanthin (ASTX) and NATURAL group (not fed with ration). 180 prawns were used, with 60 males (6.08±1.96 g) and 120 females (4.55±1.03 g) distributed in five groups containing four males and eight females each . The re were no significant differences in performance and body indexes. The number of released spermatozoids, live spermatozoids, body and egg pigmentation was higher in BIXN and ASTX treatments. The ASTX treatment was superior to the NATURAL group in the body pigmentation of females and eggs and release of spermatophores by males. These results demonstrate that the use of natural and artificial carotenoid pigments in the diet are beneficial for reproduction of M. amazonicum.
650 $aAstaxanthin
650 $aReproductive performance
650 $aBuriti
650 $aUrucum
653 $aElectroejaculation
653 $aPrawn culture
700 1 $aCASTILHO, C. de L.
700 1 $aSANTOS, U. R. A. dos
700 1 $aGEMAQUE, T. C.
700 1 $aDAMASCENO, L. F.
700 1 $aLIMA, J. de F.
700 1 $aMIRANDA FILHO, K. C.
773 $tJournal of Agricultural Studies$gv. 9, n. 2, p. 32-56, 2021.
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Registro original: |
Embrapa Amapá (CPAF-AP) |
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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. |
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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Circulação/Nível: |
A - 2 |
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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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