Base de dados : LILACS
Pesquisa : B01.650.940.800.575.912.250.456.750 [Categoria DeCS]
Referências encontradas : 3 [refinar]
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Id: biblio-1001568
Autor: Wu, Tao; Zhang, Qianrui; Song, Hongping.
Título: Swertiamarin attenuates carbon tetrachloride (CCl4)-induced liver injury and inflammation in rats by regulating the TLR4 signaling pathway
Fonte: Braz. J. Pharm. Sci. (Online);54(4):e17449, 2018. graf.
Idioma: en.
Resumo: The aim of the present study is to illustrate the effects of swertiamarin (STM), a natural iridoid from herbal medicines, on hepatic inflammation induced by carbon tetrachloride (CCl4) in rats. Male Sprague Dawley rats were exposed to CCl4 with or without STM co-administration for 8 weeks. Our results revealed that STM administration (100 and 200 mg/kg b.w.) significantly attenuated inflammation in livers of CCl4-treated rats. STM remarkably reduced the production of interleukin-1ß (IL-1ß), interleukin-6 (IL-6), tumor necrosis factor alpha (TNF-α), macrophage inflammatory protein-1a (MIP-1α), and monocyte chemotactic protein-1 (MCP-1) in liver tissue of CCl4-treated rats. In addition, STM treatment downregulated connective tissue growth factor (CTGF) and ser307pIRS-1 expression, which was induced by CCl4 exposure. In the process of exploring the anti-inflammatory mechanisms of STM action, we demonstrated that STM significantly inhibited Toll-like receptor 4 (TLR4) and nuclear factor kappa B (NF-κB) p65 expression in the liver. In conclusion, these results suggested that the inhibition of CCl4-induced inflammation by STM was, at least in part, due to its regulation of the TLR4 /NF-κB signaling pathway
Descritores: Tetracloreto de Carbono/farmacologia
Receptor 4 Toll-Like
Doença Hepática Induzida por Substâncias e Drogas/diagnóstico
-NF-kappa B
Gentianaceae/classificação
Glicosídeos/efeitos adversos
Inflamação/tratamento farmacológico
Limites: Animais
Masculino
Ratos
Responsável: BR40.1 - DBD - Divisão de Biblioteca e Documentacão do Conjunto das Químicas


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Id: lil-722791
Autor: Sánchez, Julie Andrea; Moreno-Murillo, Bárbara; Cuca Suarez, Luis Enrique.
Título: Two new secoiridoids from Chelonanthus alatus (Aubl) Pulle (Gentianaceae) / Dos nuevos secoiridoides de Chelonanthus alatus (Aubl) Pulle (Gentianaceae)
Fonte: Bol. latinoam. Caribe plantas med. aromát;12(2):186-195, mar. 2013. ilus, tab, graf.
Idioma: en.
Conferência: Apresentado em: Congress of Chemistry of Natural Products Chilean, Argentine and Hispanic, 3, Punta Arenas, Apr. 2012.
Resumo: The species Chelananthus alatus is an herbaceous plant with known ethno botanical and medicinal properties used in control of fever, especially those produced by malaria. From dried leaves (1.11 Kg), the crude alcoholic extract was fractionated by liquid-liquid partition with different polarity solvents. From the sec-butyl alcohol soluble fraction, by successive application of chromatographic methods, four compounds type iridoid were isolated and identified by spectroscopic techniques. Compound 1 is a new secoiridoid which was identified as sweroside 7-isobutyryloxy, and it is reported here for the first time in the Gentianaceae family; the other secoiridoids which were isolated are known as vogeloside (2), dihydro-chelonanthoside (3) and sweroside (4); vogeloside was identified for the first time in this plant (C. alatus). From the isopropyl acetate extract, in conjunction with the sweroside 7- isobutyryloxy (1), chelonanthoside (5) and sweroside (4), were identified, along with the sweroside 7-isovaleryloxy-(6) as a new side chain isomeric ester of dihydrochelonanthoside (3) . This work presents the spectroscopic analysis of the new structures and some bioactivity data.

La especie Chelonanthus alatus (Gentianaceae) es una hierba de aplicaciones ethnobotánicas reconocidas en medicina tradicional, especialmente en el control de la fiebre producida por la malaria. De las hojas secas (1,11 Kg) se realizó el extracto crudo en alcohol etílico, el cual se fraccionó por partición líquido-líquido (L-L) con disolventes de diferente polaridad. De la fracción soluble en alcohol sec-butílico, se aislaron cuatro compuestos tipo seco-iridoide por aplicación sucesiva de diversos métodos cromatográficos los cuales se identificaron por técnicas espectroscópicas. El compuesto 1 es un nuevo secoiridoide identificado como de 7- isobutiriloxi-swerosido, y se reporta por primera vez en la familia Gentianaceae; los otros tres secoiridoides aislados se conocen como vogelósido (2), dihidrochelonanthosido (3) y swerósido (4); el vogelósido se identificó por primera vez en C. alatus. De la fracción soluble en acetato de isopropilo además del 7-isobutiriloxi-swerosido (1) y el swerosido se aislaron e identificaron, el chelonanthosido (5) y el isovaleriloxi-swerosido (6), el cual es un nuevo isómero del dihidrochelonanthosido. En este trabajo se presenta el análisis espectroscópico que llevó a la elucidación estructural de los compuestos novedosos y algunos datos de bioactividad.
Descritores: Extratos Vegetais/química
Gentianaceae/química
Iridoides/isolamento & purificação
Iridoides/análise
-Folhas de Planta/química
Responsável: CL1.1 - Biblioteca Central


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Alecrim, Maria das Graças Costa
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Autor: Memorias do Instituto Oswaldo Cruz; Silva, Luiz Francisco Rocha e; Lima, Emerson Silva; Vasconcellos, Marne Carvalho de; Aranha, Ellen Suzany Pereira; Costa, David Siqueira; Mustafa, Elba Vieira; Morais, Sabrina Kelly Reis de; Alecrim, Maria das Gracas Costa; Nunomura, Sergio Massayoshi; Struwe, Lena; Andrade-Neto, Valter Ferreira de; Pohlit, Adrian Martin.
Título: In vitro and in vivo antimalarial activity and cytotoxicity of extracts, fractions and a substance isolated from the Amazonian plant Tachia grandiflora (Gentianaceae)
Fonte: Mem. Inst. Oswaldo Cruz;108(4):501-507, jun. 2013. tab, graf.
Idioma: en.
Projeto: CNPq; . CNPq.
Resumo: Tachia sp. are used as antimalarials in the Amazon Region and in vivo antimalarial activity of a Tachia sp. has been previously reported. Tachia grandiflora Maguire and Weaver is an Amazonian antimalarial plant and herein its cytotoxicity and antimalarial activity were investigated. Spectral analysis of the tetraoxygenated xanthone decussatin and the iridoid aglyone amplexine isolated, respectively, from the chloroform fractions of root methanol and leaf ethanol extracts was performed. In vitro inhibition of the growth of Plasmodium falciparum Welch was evaluated using optical microscopy on blood smears. Crude extracts of leaves and roots were inactive in vitro. However, chloroform fractions of the root and leaf extracts [half-maximal inhibitory concentration (IC50) = 10.5 and 35.8 µg/mL, respectively] and amplexine (IC50= 7.1 µg/mL) were active in vitro. Extracts and fractions were not toxic to type MRC-5 human fibroblasts (IC50> 50 µg/mL). Water extracts of the roots of T. grandiflora administered by mouth were the most active extracts in the Peters 4-day suppression test in Plasmodium berghei-infected mice. At 500 mg/kg/day, these extracts exhibited 45-59% inhibition five to seven days after infection. T. grandiflora infusions, fractions and isolated substance have potential as antimalarials.
Descritores: Antimaláricos/farmacologia
Fibroblastos/efeitos dos fármacos
Gentianaceae/química
Extratos Vegetais/farmacologia
Plasmodium falciparum/efeitos dos fármacos
-Antimaláricos/isolamento & purificação
INHIBITORY CONCENTRATION ACADEMIES AND INSTITUTES
Extratos Vegetais/isolamento & purificação
Limites: Animais
Humanos
Camundongos
Tipo de Publ: Research Support, Non-U.S. Gov't
Responsável: BR1.1 - BIREME



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