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1.
Sci Rep ; 12(1): 6282, 2022 04 15.
Artigo em Inglês | MEDLINE | ID: mdl-35428370

RESUMO

The ethanol extract from the wood of Taxus Yunnanensis (TY) induced apoptosis in all cancer cell lines tested, which was mainly due to activation of an extrinsic pathway in human colon cancer DLD-1 cells. The extrinsic pathway was activated by the upregulation of the expression levels of Fas and TRAIL/DR5, which led to the activation of caspase-8. Of note, the machinery of this increase in expression was promoted by the upregulation of MIR32a expression, which silenced MIR34a-targeting E2F3 transcription factor. Furthermore, ectopic expression of MIR32a or siR-E2F3 silencing E2F3 increased Fas and TRAIL/DR5 expression. Thus, the extract activated the extrinsic pathway through the MIR34a/E2F3 axis, resulting in the autocrine and paracrine release of TRAIL, and upregulated expression of death receptors Fas and DR5 in the treated DLD-1 cells, which were functionally validated by Fas immunocytochemistry, and using anti-Fas and anti-TRAIL antibodies, respectively. In vivo, TY showed significant anti-tumor effects on xenografted and syngeneic model mice. The extract may also aid in chemoprevention by selectively making marked tumor cells susceptible to the tumor immunosurveillance system.


Assuntos
Receptores do Ligante Indutor de Apoptose Relacionado a TNF , Taxus , Animais , Apoptose , Morte Celular , Linhagem Celular Tumoral , Glicoproteínas de Membrana/metabolismo , Camundongos , Extratos Vegetais/farmacologia , Receptores do Ligante Indutor de Apoptose Relacionado a TNF/metabolismo , Ligante Indutor de Apoptose Relacionado a TNF/farmacologia , Taxus/metabolismo , Madeira/metabolismo
2.
Phytochemistry ; 72(14-15): 1760-6, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21762939

RESUMO

Fluctuations in the biosynthesis of taxoids in 1-5 year old cultured seedlings of Taxus chinensis var. mairei were investigated using LC-IT-TOF-MS and a metabolomics approach. In the total ion chromatogram (TIC) of the extracts, 16 prominent peaks were observed. Ten compounds were identified by comparison of retention times and MS/MS spectra with those of reference compounds. An additional 6 taxoids were isolated by preparative HPLC and identified by comparison of their spectroscopic data with those reported in the literature. It was clarified that the relative concentrations of taxoids with 4(20) double bonds are high at early stages of cultivation. On the other hand, relatively higher amounts of 5-acetoxy taxoids oxidized at the 4- and 10- positions and taxoids having 5(20)-oxetane rings were found at later stages of cultivation. This approach provides practical information on the biosynthetic flow of taxoids in cultured yew seedlings.


Assuntos
Metabolômica/métodos , Extratos Vegetais/química , Taxoides/análise , Taxus/química , Cromatografia Líquida , Estrutura Molecular , Plantas Medicinais/química , Plântula/química , Espectrometria de Massas em Tandem , Taxoides/química , Taxoides/isolamento & purificação , Madeira/química
3.
J Nat Prod ; 74(1): 102-5, 2011 Jan 28.
Artigo em Inglês | MEDLINE | ID: mdl-21138310

RESUMO

From the aqueous extract of the wood of Taxus yunnanensis, which showed cytochrome P450 3A4 (CYP3A4) inhibition, a new isoflavan [(3S,4R)-4'-hydroxy-6,3'-dimethoxyisoflavan-4-ol (1)], a new degraded lignan [2,3-bis(hydroxymethyl)-7-hydroxy-6-methoxy-1-tetralone (2)], and a new lignan [(7R)-7-hydroxytaxiresinol (3)] were isolated, together with nine known lignans. Among the isolates obtained, α-conidendrin (12) showed strong CYP3A4 inhibition with an IC(50) value of 0.2 µM.


Assuntos
Antineoplásicos Fitogênicos/isolamento & purificação , Antineoplásicos Fitogênicos/farmacologia , Antioxidantes/isolamento & purificação , Antioxidantes/farmacologia , Colletotrichum/química , Inibidores do Citocromo P-450 CYP3A , Sequestradores de Radicais Livres/isolamento & purificação , Sequestradores de Radicais Livres/farmacologia , Furanos/isolamento & purificação , Furanos/farmacologia , Isocumarinas/isolamento & purificação , Isocumarinas/farmacologia , Isoflavonas/isolamento & purificação , Isoflavonas/farmacologia , Lignanas/isolamento & purificação , Lignanas/farmacologia , Tetra-Hidronaftalenos/isolamento & purificação , Tetra-Hidronaftalenos/farmacologia , Antineoplásicos Fitogênicos/química , Antioxidantes/química , Compostos de Bifenilo/farmacologia , Citocromo P-450 CYP3A , Ensaios de Seleção de Medicamentos Antitumorais , Sequestradores de Radicais Livres/química , Furanos/química , Células Hep G2 , Humanos , Isocumarinas/química , Isoflavonas/química , Lignanas/química , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular , Picratos/farmacologia , Taxus/microbiologia , Tetra-Hidronaftalenos/química , Madeira/química
4.
Nat Prod Commun ; 5(10): 1551-6, 2010 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21121246

RESUMO

The fragmentation pathways of seven types of taxoids were investigated by using a LC-MS/MS method, namely: (1) neutral taxoids with a C-4(20) double bond; (2) taxoids with a C-4(20) double bond and oxygenation at C-14; (3) 5-cinnamoyl taxoids with a C-4(20) double bond; (4) a basic taxoid with a C-4(20) double bond; (5) a taxoid with a C-4(20) epoxide; (6) taxoids with an oxetane ring; and (7) taxoids with an oxetane ring and a phenylisoserine C-13 side chain. Depending on the class of core structure and the substitution pattern, each taxoid gave either the molecular adduct ion [M+NH4]+ or [M+H]+. In the MS/MS, the molecular adduct ion gave characteristic product ions corresponding to the loss of water, acetic acid, benzoic acid, and cinnamic acid or the phenylisoserine group. These could reflect the difference of the substitutions and structural modifications and should be utilized for the structure elucidation oftaxoids by LC-MS.


Assuntos
Taxoides/química , Cromatografia Líquida , Espectrometria de Massas por Ionização por Electrospray , Espectrometria de Massas em Tandem , Taxoides/isolamento & purificação
5.
Biol Pharm Bull ; 29(11): 2310-2, 2006 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17077536

RESUMO

The H2O, H2O/MeOH (1:1) extracts from the wood of Taxus yunnanensis showed a remarkable inhibitory effect on induced histamine release from the human basophilic cell line, KU812. The eleven constituents purified from the wood extracts of Taxus yunnanensis were tested by an in vitro histamine release inhibition assay. Among them, secoisolarciresinol and taxiresinol were found to show inhibitory activities. A new neolignan, 2-[2-hydroxy-5-(3-hydroxypropyl)-3-methoxyphenyl]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol, was isolated from the wood of Taxus yunnanensis.


Assuntos
Antialérgicos/farmacologia , Medicamentos de Ervas Chinesas/farmacologia , Extratos Vegetais/farmacologia , Taxus/química , Antialérgicos/química , Antialérgicos/isolamento & purificação , Butileno Glicóis/química , Butileno Glicóis/isolamento & purificação , Butileno Glicóis/farmacologia , Calcimicina/farmacologia , Isótopos de Carbono , Linhagem Celular , Cromatografia Líquida de Alta Pressão , Deutério , Medicamentos de Ervas Chinesas/química , Medicamentos de Ervas Chinesas/isolamento & purificação , Furanos/química , Furanos/isolamento & purificação , Furanos/farmacologia , Liberação de Histamina/efeitos dos fármacos , Humanos , Lignanas/química , Lignanas/isolamento & purificação , Lignanas/farmacologia , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular , Fenóis/química , Fenóis/isolamento & purificação , Fenóis/farmacologia , Casca de Planta/química , Extratos Vegetais/química , Extratos Vegetais/isolamento & purificação , Propilenoglicóis/química , Propilenoglicóis/isolamento & purificação , Propilenoglicóis/farmacologia , Espectrofotometria Infravermelho , Taxoides/química , Taxoides/isolamento & purificação , Taxoides/farmacologia , Madeira/química
6.
Planta Med ; 72(13): 1241-4, 2006 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-16902867

RESUMO

The wood of Taxus yunnanensis (Taxaceae) showed growth inhibitory activities against human cancer cell lines, such as cervical HeLa adenocarcinoma. The morphological changes indicated that the cellular growth inhibitions were caused by apoptosis. To determine the active components, T. yunnanensis wood was analyzed by using a liquid chromatography-Fourier-transform MS (LC/FT-MS) technique. As a result, taxane-type diterpenes, such as 10-deacetylcephalomannine and 10-deacetyltaxol, were found to be present in amounts consistent with the growth inhibitory activity.


Assuntos
Antineoplásicos Fitogênicos/farmacologia , Diterpenos/farmacologia , Taxus/química , Antineoplásicos Fitogênicos/química , Antineoplásicos Fitogênicos/isolamento & purificação , Divisão Celular/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Cromatografia Líquida , Diterpenos/química , Diterpenos/isolamento & purificação , Análise de Fourier , Células HeLa , Humanos , Espectrometria de Massas , Casca de Planta/química , Madeira/química
7.
Life Sci ; 74(22): 2781-92, 2004 Apr 16.
Artigo em Inglês | MEDLINE | ID: mdl-15043992

RESUMO

The effects of secoisolariciresinol (1) and isotaxiresinol (2), two major lignans isolated from the wood of Taxus yunnanensis, on tumor necrosis factor-alpha (TNF-alpha)-dependent hepatic apoptosis induced by D-galactosamine (d-GalN)/lipopolysaccharide (LPS) were investigated in mice. Co-administration of d-GalN (700 mg/kg) and LPS (10 microg/kg) resulted in a typical hepatic apoptosis characterized by DNA fragmentation and the formation of apoptotic bodies. Serum glutamic pyruvic transaminase (sGPT) and glutamic oxaloacetic transaminase (sGOT) levels were also raised at 8 h after d-GalN/LPS intoxication due to a severe necrosis of hepatocytes. Pre-administration of 1 or 2 (50, 10 mg/kg, i.p.) 12 and 1 h before d-GalN/LPS significantly reduced DNA fragmentation and prevented chromatin condensation, apoptotic body formation and hepatitis. Pro-inflammatory cytokines such as TNF-alpha and interferon-gamma (IFN-gamma) secreted from LPS-activated macrophages are important mediators of hepatocyte apoptosis in this model. Pre-treatment with 1 or 2 significantly inhibited the elevation of serum TNF-alpha and IFN-gamma levels. In a separate experiment, both lignans had a significant dose-dependent protective effect on d-GalN/TNF-alpha-induced cell death in primary cultured mouse hepatocytes and TNF-alpha-mediated cell death in murine L929 fibrosarcoma cells. These results indicated that 1 and 2 prevent d-GalN/LPS-induced hepatic injury by inhibiting hepatocyte apoptosis through the blocking of TNF-alpha and IFN-gamma production by activated macrophages and direct inhibition of the apoptosis induced by TNF-alpha.


Assuntos
Apoptose/efeitos dos fármacos , Butileno Glicóis/farmacologia , Doença Hepática Induzida por Substâncias e Drogas/prevenção & controle , Furanos/farmacologia , Lignanas , Extratos Vegetais/farmacologia , Fator de Necrose Tumoral alfa , Alanina Transaminase/sangue , Animais , Aspartato Aminotransferases/sangue , Butileno Glicóis/administração & dosagem , Butileno Glicóis/uso terapêutico , Doença Hepática Induzida por Substâncias e Drogas/sangue , Doença Hepática Induzida por Substâncias e Drogas/etiologia , Relação Dose-Resposta a Droga , Quimioterapia Combinada , Furanos/administração & dosagem , Furanos/uso terapêutico , Galactosamina/farmacologia , Injeções Intraperitoneais , Interferon gama/sangue , Lipopolissacarídeos/farmacologia , Fígado/efeitos dos fármacos , Fígado/metabolismo , Fígado/patologia , Masculino , Camundongos , Camundongos Endogâmicos , Fitoterapia , Extratos Vegetais/administração & dosagem , Extratos Vegetais/uso terapêutico , Plantas Medicinais , Taxus , Fator de Necrose Tumoral alfa/análise , Fator de Necrose Tumoral alfa/metabolismo
8.
Planta Med ; 70(1): 29-33, 2004 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-14765289

RESUMO

The hepatoprotective effect of taxiresinol ( 1) and (7' R)-7'-hydroxylariciresinol ( 2), two tetrahydrofuran-type lignans isolated from the wood of Taxus yunnanensis, were investigated on D-galactosamine ( D-GalN)/lipopolysaccharide (LPS)-induced hepatic liver injury in mice. Pre-administration of 1 or 2 at doses of 50 and 10 mg/kg ( i. p.) at 12 and 1 h before D-GalN/LPS injection significantly inhibited hepatocyte DNA fragmentation and apoptotic body formation. Pre-treatment of these two lignans further suppressed hepatic necrosis which occur at later stage of D-GalN/LPS intoxication as demonstrated by the significant and dose-dependent reduction in serum glutamic pyruvic transaminase (sGPT) and serum glutamic oxaloacetic transaminase (sGOT) at 8 h after intoxication. The elevation of serum tumor necrosis factor-alpha (TNF- alpha) level by D-GalN/LPS toxication was significantly inhibited by 1 or 2 at doses of 50 and 10 mg/kg. Moreover, both of these lignans significantly protected hepatocytes from D-GalN/TNF- alpha-induced cell death in primary cultured mouse hepatocytes. These results suggested that 1 and 2 had protected the hepatocytes from apoptosis via an inhibition of TNF- alpha production by activated macrophages and a direct inhibition of apoptosis induced by TNF- alpha in D-GalN/LPS-treated mice.


Assuntos
Doença Hepática Induzida por Substâncias e Drogas/prevenção & controle , Furanos/farmacologia , Fitoterapia , Extratos Vegetais/farmacologia , Plantas Medicinais , Substâncias Protetoras/farmacologia , Árvores , Animais , Doença Hepática Induzida por Substâncias e Drogas/etiologia , Furanos/administração & dosagem , Furanos/uso terapêutico , Galactosamina , Lignanas , Lipopolissacarídeos , Masculino , Camundongos , Extratos Vegetais/administração & dosagem , Extratos Vegetais/uso terapêutico , Substâncias Protetoras/administração & dosagem , Substâncias Protetoras/uso terapêutico
9.
Phytochemistry ; 64(6): 1141-7, 2003 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-14568081

RESUMO

Two taxane-type diterpenes, 10beta-acetoxy-2alpha,5alpha,7beta,9alpha-tetrahydroxytaxa-4(20),11-dien-13-one and 2alpha-acetoxy-9alpha-benzoyloxy-5alpha,7beta,10beta,15-tetrahydroxy-11(15-->1)- abeotaxa-4(20),11-dien-13-one, and two new drimane-type sesquiterpenes, 1beta-acetoxy-7-drimen-11alpha-ol-12,11-lactone and 1beta-acetoxy-11,12-epoxy-6-drimen-8alpha,11alpha-diol, were isolated from the bark of Taxus yunnanensis together with 35 known taxane-type diterpenes, a known drimane-type sesquiterpene and a known flavanone.


Assuntos
Diterpenos/isolamento & purificação , Casca de Planta/química , Sesquiterpenos/isolamento & purificação , Taxus/química , Diterpenos/química , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular , Sesquiterpenos/química
10.
Planta Med ; 69(6): 500-5, 2003 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12865966

RESUMO

The H2O, H2O/MeOH (1 : 1) and MeOH extracts of the wood of Taxus yunnanensis possessed significant DPPH radical scavenging and nitric oxide (NO) inhibitory activities. Chemical investigation of these extracts led us to isolation of nineteen compounds, i. e., five lignans, two simple phenolics, and twelve taxane-type diterpenes. Isotaxiresinol and seco-isolariciresinol, two major lignans of the wood, possessed potent DPPH radical scavenging activities with IC 50 values of 21.7 and 28.9 microM, respectively. Similarly, coniferyl aldehyde, taxusin, 10-deacetyltaxuyunnanine C, hongdoushan A, and 2alpha,5alpha,10beta-triacetoxy-14beta-[( S)-2-methylbutyryloxy]-4(20),11-taxadiene showed potent NO inhibitory activity with IC 50 values of 18.0, 22.1, 28.5, 15.0 and 26.4 microM, respectively, which were either equal or lower than the positive control NG-monomethyl- L-arginine ( L -NMMA) with an IC 50 value of 28.5 microM.


Assuntos
Antioxidantes/farmacologia , Óxido Nítrico/antagonistas & inibidores , Fitoterapia , Extratos Vegetais/farmacologia , Taxus , Animais , Antioxidantes/administração & dosagem , Antioxidantes/uso terapêutico , Compostos de Bifenilo , Relação Dose-Resposta a Droga , Humanos , Concentração Inibidora 50 , Lipopolissacarídeos/farmacologia , Macrófagos/efeitos dos fármacos , Macrófagos/metabolismo , Camundongos , Óxido Nítrico/metabolismo , Picratos , Extratos Vegetais/administração & dosagem , Extratos Vegetais/uso terapêutico , Células Tumorais Cultivadas/efeitos dos fármacos , Madeira
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