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1.
Artigo em Inglês | MEDLINE | ID: mdl-28326124

RESUMO

Impatiens balsamina L. (Balsaminaceae), an annual herb found throughout China, has been extensively used in traditional Chinese medicine (TCM). However, our knowledge regarding the adverse effects of I. balsamina in vivo is very limited. In this present study, the nematode Caenorhabditis elegans model was employed to fully assess the adverse effects of hydroalcoholic (EtOH 55%) extracts of I. balsamina stems (HAEIBS) in vivo. After exposure to 10 mg/mL HAEIBS, the major organism-level endpoints of C. elegans of percent survival, frequency of head thrash and body bends, and reproduction had decreased by 24%, 30%, and 25%, respectively. The lifespan of C. elegans was also greatly reduced after HAEIBS exposure compared to the controls. The active compounds in HAEIBS were separated using high speed countercurrent chromatograph (HSCCC) and characterized by high performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR). Two compounds, lawsone and 2-methoxy-1,4-naphthoquinone (MNQ), and their adverse effects were then more thoroughly detailed in this study. It was found that lawsone is the major toxin in HAEIBS with a higher toxicity than MNQ in terms of negative impact on C. elegans mortality, locomotion, reproduction, and lifespan. Our data also suggests that the C. elegans model may be useful for assessing the possible toxicity of other Chinese medicines, plant extracts, and/or compounds.

2.
Nat Prod Res ; 30(1): 35-41, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-25894611

RESUMO

Seeds of Cassia obtusifolia L. are known as homology of medicine and food material, which is a commonly consumed beverage in China. One new compound, 8-hydroxy-1,7-dimethoxy-3-methylanthracene-9,10-dione-2-O-ß-d-glucoside (1), together with 11 known compounds, including seven anthraquinones (2-8), was isolated from the seeds. The 2D NMR data of compound 2 are reported for the first time. The structures of the compounds were established on the basis of 1D and 2D NMR, IR and HR-ESI-MS spectra. The cytotoxic activities of all the compounds against five cell lines (LO2, HCT-116, A549, HepG2 and SGC7901) were evaluated by using CCK8 methods. Compounds 1, 3 and 7 show moderate cytotoxicity towards HCT-116 cells compared with oxaliplatin.


Assuntos
Antraquinonas/isolamento & purificação , Antraquinonas/farmacologia , Cassia/química , Sementes/química , Antraquinonas/química , Antineoplásicos Fitogênicos/química , Antineoplásicos Fitogênicos/farmacologia , Linhagem Celular Tumoral/efeitos dos fármacos , China , Ensaios de Seleção de Medicamentos Antitumorais/métodos , Glucosídeos/química , Glucosídeos/farmacologia , Células HCT116/efeitos dos fármacos , Células Hep G2/efeitos dos fármacos , Humanos , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Compostos Organoplatínicos/farmacologia , Oxaliplatina , Espectrometria de Massas por Ionização por Electrospray
3.
Zhong Yao Cai ; 38(6): 1206-8, 2015 Jun.
Artigo em Chinês | MEDLINE | ID: mdl-26762061

RESUMO

OBJECTIVE: To investigate the steroidal glycoside constituents of Solanum cumingii. METHODS: The compounds were isolated by silica gel, Sephadex LH-20, RP-C18 column and Pre-HPLC chromatography. Their structures were identified by ESI-MS and NMR. RESULTS: Six known compounds including torvoside K (1), torvoside J (2), torvoside L (3), khasianine (4), aculeatiside A (5) and solamargine (6) were isolated from Solanum cumingii. CONCLUSION: All compounds are isolated from Solanum cumingii for the first time.


Assuntos
Glicosídeos/química , Solanum/química , Cromatografia Líquida de Alta Pressão , Espectroscopia de Ressonância Magnética , Fitosteróis , Alcaloides de Solanáceas , Espirostanos
4.
Oncol Lett ; 8(3): 1139-1142, 2014 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-25120673

RESUMO

Daphnoretin is an active constituent of Wikstroemia indica C.A. Mey., which is widely distributed in the northwest and southwest regions of China. Previous studies have shown that daphnoretin has anticancer effects on leukemia, osteosarcoma and uterine cervix cancer cells. However, the effect of daphnoretin on human lung cancer cells has yet to be elucidated. In the present study, daphnoretin was observed to inhibit A549 lung cancer cell proliferation in a concentration- and time-dependent manner. Fluorescent microscopy and flow cytometric analysis showed that daphnoretin induced A549 cell apoptosis in a concentration-dependent manner. Western blot analysis also revealed that daphnoretin induced apoptosis through the regulation of the B-cell lymphoma-2 gene family in A549 cells. These findings indicate that daphnoretin may have potential as a therapeutic agent for the management of lung cancer.

5.
Anticancer Drugs ; 25(9): 1072-80, 2014 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-25035959

RESUMO

Leukemia is currently one of the most deadly diseases. Ginseng has been used in Asian countries for the treatment and prevention of various diseases, including leukemia, but the molecular mechanism of its antileukemia activity has not been well defined. The aim of this study was to explore the effect of 20-(s)-ginsenoside Rg3 on apoptosis in human leukemic U937 and HL-60 cells and the underlying mechanism. We found that 20-(s)-ginsenoside Rg3 reduced cell viability and induced apoptosis in U937 and HL-60 cells. The induction of apoptosis was accompanied by the downregulation of PI3K/Akt family proteins. Moreover, we observed that 20-(s)-ginsenoside Rg3 treatment resulted in activation of caspase-3 and caspase-9. Taken together, our findings suggest for the first time that 20-(s)-ginsenoside Rg3 can promote apoptosis in U937 and HL-60 cells, at least partly through the downregulation of PI3K/Akt family proteins. Moreover, the triggering of caspase-3 and caspase-9 activation mediated apoptotic induction. All these findings collectively demonstrate that the natural compound 20-(s)-ginsenoside Rg3 effectively induces apoptosis in human leukemic cells, which suggests that this compound may play a role in future therapies for leukemia.


Assuntos
Antineoplásicos/farmacologia , Apoptose/efeitos dos fármacos , Ginsenosídeos/farmacologia , Proteína Oncogênica v-akt/metabolismo , Fosfatidilinositol 3-Quinases/metabolismo , Caspase 3/metabolismo , Caspase 9/metabolismo , Proliferação de Células/efeitos dos fármacos , Cromonas/farmacologia , Células HL-60/efeitos dos fármacos , Humanos , Leucemia/tratamento farmacológico , Morfolinas/farmacologia , Fosforilação , Transdução de Sinais , Serina-Treonina Quinases TOR/metabolismo , Células U937/efeitos dos fármacos
6.
Zhong Yao Cai ; 31(3): 374-6, 2008 Mar.
Artigo em Chinês | MEDLINE | ID: mdl-18619239

RESUMO

OBJECTIVE: To study the constituents isolated from Juncus effuses Linn.. METHODS: The compounds were isolated through chromatographic approaches, such as Silica gel. CC, Sephadex LH-20 and were identified by a combination of spectroscopic methods (UV, MS, 1H-NMR, 13C-NMR and NOE). RESULTS: 8 kinds of compounds were identified which included four flavonoids, luteolin (I), eriodictyol (II), 2', 5', 5, 7-tetrahydroxyflavone (III), glucoluteolin (IV); two aromatic compounds, methyl p-hydroxybenzoate (V), vanillic acid (VI); a fatty acid, hexadecanoic acid (I) and an alkane, n-Tetradecane (VIII). CONCLUSION: Compound II, III, V, VI, VII, VIII were firstly isolated from this plant.


Assuntos
Ácidos Graxos/isolamento & purificação , Flavonoides/isolamento & purificação , Magnoliopsida/química , Parabenos/isolamento & purificação , Plantas Medicinais/química , Alcanos/química , Alcanos/isolamento & purificação , Ácidos Graxos/química , Flavonoides/química , Luteolina/química , Luteolina/isolamento & purificação , Ácido Palmítico/química , Ácido Palmítico/isolamento & purificação , Parabenos/química , Ácido Vanílico/química , Ácido Vanílico/isolamento & purificação
7.
Zhong Yao Cai ; 30(5): 513-5, 2007 May.
Artigo em Chinês | MEDLINE | ID: mdl-17727052

RESUMO

OBJECTIVE: To compare the quality of cultivated Chinese yam (Dioscorea polystachya Turcz.) from Yunnan (Kunming yam) and Henan (Tiegum yam) by determining the content of dry substance in fresh sample and the contents of water extracts, ethanol extracts, starch, protein, crude-fat and polysaccharide in dry sample. METHOD: The above-mentioned indexes were determined by methods of air desiccation, cold-immersing, hot-immersing, iodine-blue coloration, half Micro-Kjeldahl, Soxhlet extraction and spectrophotometric method respectively. RESULT: In fresh sample, the content of dry substance of Kunming yam is a little lower than Tiegun yam; in dry sample, all indexes of Kunming yam are higher than or approach to those of Tiegun yam except the content of crude-fat. Especially the content of polysaccharide in Kunming yam is 64% higher than that of Tiegun yam. CONCLUSION: Kunming yam, with high quality, high yield and good taste, deserves paying close attention as a good variety.


Assuntos
Dioscorea/química , Proteínas de Plantas/análise , Plantas Medicinais/química , Polissacarídeos/análise , China , Dioscorea/crescimento & desenvolvimento , Gorduras/análise , Gorduras/isolamento & purificação , Proteínas de Plantas/isolamento & purificação , Tubérculos/química , Tubérculos/crescimento & desenvolvimento , Plantas Comestíveis/química , Plantas Comestíveis/crescimento & desenvolvimento , Plantas Medicinais/crescimento & desenvolvimento , Polissacarídeos/isolamento & purificação , Controle de Qualidade , Especificidade da Espécie
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