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1.
Am J Chin Med ; 30(2-3): 315-25, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12230020

RESUMO

Two components of garlic, diallyl sulfide (DAS) and diallyl disulfide (DADS), inhibited arylamine N-acetyltransferase (NAT) activity and 2-aminofluorene-DNA adduct in human promyelocytic leukemia cells (HL-60). The NAT activity was measured by high performance liquid chromatography assaying for amounts of N-acetyl-2-aminofluorene (2-AAF) and remaining 2-aminofluorene (2-AF). Cellular cytosols and intact cell suspensions were assayed. The inhibition of NAT activity and 2-AF-DNA adduct formation in human leukemia cells by DAS and DADS were dose-dependent and were directly proportional. The data also indicated that DAS and DADS decrease the apparent values of Km and Vmax from human leukemia cells in both assays. This is the first report of garlic components affecting human leukemia cell NAT activity and 2-AF-DNA adduct formation.


Assuntos
Compostos Alílicos/uso terapêutico , Anticarcinógenos/uso terapêutico , Adutos de DNA/efeitos dos fármacos , Dissulfetos/uso terapêutico , Alho , Leucemia Promielocítica Aguda/prevenção & controle , Fitoterapia , Sulfetos/uso terapêutico , Compostos Alílicos/administração & dosagem , Compostos Alílicos/farmacologia , Anticarcinógenos/administração & dosagem , Anticarcinógenos/farmacologia , Arilamina N-Acetiltransferase/efeitos dos fármacos , Adutos de DNA/química , Adutos de DNA/metabolismo , Dissulfetos/administração & dosagem , Dissulfetos/farmacologia , Relação Dose-Resposta a Droga , Fluorenos/química , Fluorenos/metabolismo , Células HL-60/efeitos dos fármacos , Humanos , Óleos de Plantas/administração & dosagem , Óleos de Plantas/farmacologia , Óleos de Plantas/uso terapêutico , Sulfetos/administração & dosagem , Sulfetos/farmacologia
2.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 21(6): 427-30, 2001 Jun.
Artigo em Chinês | MEDLINE | ID: mdl-12577437

RESUMO

OBJECTIVE: To investigate the clinical efficacy of Tianfoshen oral liquid (TFS) in treating moderate and advanced malignant tumors and its mechanism. METHODS: Therapeutic effect of TFS in treating 71 patients of malignant tumor was analyzed with the criteria, including quality of life, 3-year survival rate and immune function. And experimental studies of inhibitory effect on tumor clone primordial cells and tumor growth rate of TFS on human gastric tumor (MGC803) cell, human liver cancer (SMMC7721) cell and mice galactophore cancer (EMT6) cell by colony forming method and dye exclusion test respectively were also conducted. RESULTS: Clinical study showed that in the 71 cases treated, the total remission rate was 45.1%, the effective rate 71.8%, with improvement in quality of life and immune function, the 1-, 2- and 3-year survival rate being 78.5%, 38.5% and 10.8% respectively and the mean survival time 24.2 months. Experimental study showed that TFS could kill the cancer cells directly, inhibit the proliferation of single clonogenic cell, and had a broad-spectrum dose-dependent inhibitory action on various tumors with significant difference in comparing with the effects of the control (P < 0.05). CONCLUSION: TFS had obvious therapeutic effect to moderate and advanced tumors, its anti-tumor effect was related to the enhancement of immune function and tumor inhibiting or direct killing action.


Assuntos
Antineoplásicos Fitogênicos/uso terapêutico , Medicamentos de Ervas Chinesas/uso terapêutico , Neoplasias Esofágicas/tratamento farmacológico , Neoplasias Gástricas/tratamento farmacológico , Adulto , Idoso , Idoso de 80 Anos ou mais , Antineoplásicos Fitogênicos/farmacologia , Medicamentos de Ervas Chinesas/farmacologia , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Fitoterapia , Neoplasias Gástricas/patologia , Células Tumorais Cultivadas
3.
Am J Chin Med ; 28(2): 227-38, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-10999441

RESUMO

Berberine is an alkaloid occurring in the plant genera Berberis and Coptis. Although berberine had been demonstrated to have antineoplastic function by inhibiting DNA-synthesis in activated lymphocytes, there is no available information to address berberine affects on human leukemia cell N-acetyltransferase (NAT) activity and 2-aminofluorene (AF)-DNA adduct formation. Thus, berberine was tested for inhibition of arylamine NAT activity and AF-DNA adduct formation in human leukemia cells. The NAT activity was measured by a high performance liquid chromatography assaying for the amounts of N-acetyl-2-aminofluorene (AAF) and N-acetyl-p-aminobenzoic acid (N-Ac-PABA) and the remaining AF and p-aminobenzoic acid (PABA). The NAT activity and AF-DNA adduct formation in human leukemia cells were inhibited by berberine in a dose-dependent manner, i.e. the higher the concentration of berberine, the higher the inhibition of NAT activity and AF-DNA adduct. The data also indicate that berberine decreased the apparent values of Km and Vmax from human leukemia cells in both cytosol and intact cells.


Assuntos
Antineoplásicos/farmacologia , Arilamina N-Acetiltransferase/efeitos dos fármacos , Berberina/farmacologia , Carcinógenos/metabolismo , Adutos de DNA/efeitos dos fármacos , Fluorenos/metabolismo , Leucemia Mieloide/metabolismo , Carcinógenos/química , Adutos de DNA/química , Medicamentos de Ervas Chinesas/farmacologia , Fluorenos/química , Células HL-60/efeitos dos fármacos , Células HL-60/enzimologia , Células HL-60/metabolismo , Humanos , Leucemia Mieloide/enzimologia , Leucemia Mieloide/patologia
4.
Am J Chin Med ; 27(2): 265-75, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-10467460

RESUMO

Berberine was used to determine loss of viable cells and inhibition of arylamine Nacetyltransferase (NAT) activity in a human colon tumor (adenocarcinoma) cell line. The viable cells were determined by trypan blue exclusion under a light microscope. The NAT activity was measured by high performance liquid chromatography for the amounts of N-acetyl-2-aminofluorene (AAF), N-acetyl-p-aminobenzoic acid (N-Ac-PABA), and the remaining 2-aminofluorene (AF) and p-aminobenzoic acid (PABA). The viability and NAT activity in a human colon tumor cell line was inhibited by berberine in a dose-dependent manner, i.e., the higher the concentration of berberine, the higher the inhibition of NAT activity and cell death. The NAT activities measured in the intact human colon tumor cells were decreased over 50% by AAF and NAc-PABA production from acetylation of AF and PABA. The apparent values of Kmoff and Vmax of NAT from colon tumor cells were also inhibited by berberine in cytosols and in intact cells. This report is the first to show that berberine did affect human colon tumor cell NAT activity.


Assuntos
Adenocarcinoma/enzimologia , Arilamina N-Acetiltransferase/metabolismo , Berberina/farmacologia , Neoplasias do Colo/enzimologia , Ácido 4-Aminobenzoico/toxicidade , Aflatoxinas/toxicidade , Carcinógenos/toxicidade , Sobrevivência Celular/efeitos dos fármacos , Citosol/efeitos dos fármacos , Citosol/metabolismo , Humanos , Células Tumorais Cultivadas
5.
J Appl Toxicol ; 19(2): 75-81, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-10215179

RESUMO

Arylamine N-acetyltransferase (NAT) activities with 2-aminofluorene (2-AF) were determined in the bacterium Klebsiella pneumoniae. Cytosols or suspensions of K. pneumoniae with or without specific concentrations of diallyl sulphide (DAS) or diallyl disulphide (DADS) as co-treatment showed different percentages of 2-AF acetylation. The data indicated that there was decreased NAT activity associated with increased levels of DAS or DADS in K. pneumoniae. In growth studies on K. pneumoniae it was demonstrated that DAS or DADS elicited a dose-dependent bacteriocide effect on K. pneumoniae. For the cytosol examinations, the apparent values of Km and Vmax were 0.96+/-0.09 mM and 7.87+/-0.79 nmol min(-1) mg(-1) protein, respectively, for 2-AF. However, when DAS or DADS was added to the reaction mixtures, the apparent values of Km and Vmax were 0.16+/-0.04 mM and 0.99+/-0.16 nmol min(-1) mg(-1) protein with DAS, respectively, and 0.14+/-0.18 mM and 0.85+/-0.10 nmol min(-1) mg(-1) protein with DADS, respectively, for 2-AF. For the intact bacteria examination, the apparent values of Km and Vmax were 0.57+/-0.06 mM and 2.00+/-0.14 nmol min(-1) per 10x10(10) CFU, respectively, for 2-AF. However, when DAS or DADS was added to the reaction mixtures, the apparent of values of Km and Vmax were 0.41+/-0.04 mM and 1.30+/-0.10 nmol min(-1) per 10x10(10) CFU with DAS, respectively, and 0.34+/-0.04 mM and 1.08+/-0.08 nmol min(-1) per 10x10(10) CFU with DADS, respectively, for 2-AF. This report is the first demonstration to show that the garlic components DAS and DADS would affect K. pneumoniae growth and NAT activity.


Assuntos
Compostos Alílicos/farmacologia , Anticarcinógenos/farmacologia , Arilamina N-Acetiltransferase/metabolismo , Dissulfetos/farmacologia , Alho , Klebsiella pneumoniae/efeitos dos fármacos , Plantas Medicinais , Sulfetos/farmacologia , 2-Acetilaminofluoreno/metabolismo , Acetilação , Citosol/efeitos dos fármacos , Citosol/enzimologia , Relação Dose-Resposta a Droga , Alho/química , Humanos , Klebsiella pneumoniae/enzimologia , Klebsiella pneumoniae/crescimento & desenvolvimento
6.
Am J Chin Med ; 26(3-4): 353-64, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-9862023

RESUMO

Arylamine N-acctyltransferase (NAT) activities with p-aminobenzoic acid (PABA) and 2-aminofluorene (2-AF) were determined in the bacterium Helicobacter pylori collected from peptic ulcer patients. Two assay systems were performed, one with cellular cytosols, the other with intact cell suspensions. Cytosols or suspensions of H. pylori with or without specific concentrations of diallyl sulfide (DAS) or diallyl disulfide (DADS) co-treatment showed different percentages of 2-AF and PABA acetylation. The data indicated that there was decreased NAT activity associated with increased levels of DAS or DADS in H. pylori cytosols and suspensions. Viability studies on H. pylori demonstrated that DAS or DADS elicited dose-dependent bactericide affects on H. pylori cultures. The data also indicated that DAS and DADS decreased the apparent values of K(m) and Vmax of NAT enzyme from H. pylori in both systems examined. This report is the first demonstration that garlic components can affect H. pylori growth and NAT activity.


Assuntos
Compostos Alílicos/farmacologia , Arilamina N-Acetiltransferase/metabolismo , Dissulfetos/farmacologia , Alho , Helicobacter pylori/efeitos dos fármacos , Helicobacter pylori/enzimologia , Úlcera Péptica/microbiologia , Plantas Medicinais , Sulfetos/farmacologia , Antibacterianos/farmacologia , Arilamina N-Acetiltransferase/antagonistas & inibidores , Relação Dose-Resposta a Droga , Ativação Enzimática/efeitos dos fármacos , Inibidores Enzimáticos/farmacologia , Alho/química , Infecções por Helicobacter/microbiologia , Helicobacter pylori/crescimento & desenvolvimento , Humanos , Cinética , Testes de Sensibilidade Microbiana , Óleos de Plantas/química
7.
Food Chem Toxicol ; 36(9-10): 761-70, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-9737423

RESUMO

Diallyl sulfide (DAS) and diallyl disulfide (DADS), major components of garlic, were used to determine inhibition of arylamine N-acetyltransferase (NAT) activity in a human colon tumour (adenocarcinoma) cell line. Two assay systems were performed, one with cellular cytosols (9000g supernatant), the other with intact bacterial cell suspensions. The NAT activity in a human colon tumour cell line was inhibited by DAS and DADS in a dose-dependent manner in both system: that is, the greater the concentration of DAS and DADS in the reaction, the greater the inhibition of NAT activities in both systems. The data also indicated that DAS and DADS decrease the apparent values of Km and Vmax of NAT enzymes from human colon tumour cells in both systems examined. This is the first report to demonstrate that garlic components do affect human colon tumour cell NAT activity.


Assuntos
Adenocarcinoma/enzimologia , Compostos Alílicos/farmacologia , Antineoplásicos/farmacologia , Arilamina N-Acetiltransferase/antagonistas & inibidores , Neoplasias do Colo/enzimologia , Dissulfetos/farmacologia , Alho , Plantas Medicinais , Sulfetos/farmacologia , 2-Acetilaminofluoreno/metabolismo , Ácido 4-Aminobenzoico/metabolismo , Citosol/efeitos dos fármacos , Citosol/enzimologia , Relação Dose-Resposta a Droga , Inibidores Enzimáticos/farmacologia , Humanos , Cinética , Células Tumorais Cultivadas/efeitos dos fármacos
8.
Zhongguo Zhong Yao Za Zhi ; 18(3): 156-7, 191, 1993 Mar.
Artigo em Chinês | MEDLINE | ID: mdl-8352901

RESUMO

The content of baicalin is stable when baicalin is added quantitatively in preparation. The time of extraction of the effective components of SHL with alcohol and the concentration of alcohol have little effect on the content of baicalin. The components can be extracted once, and the content of alcohol is preferably 85%. The pH level has greater influence on the content of baicalin, and should be controlled between 7.0 to 8.0. 0.2% activated carbon is suitable in preparation.


Assuntos
Medicamentos de Ervas Chinesas/química , Flavonoides/análise , Carvão Vegetal , Medicamentos de Ervas Chinesas/normas , Concentração de Íons de Hidrogênio , Controle de Qualidade , Tecnologia Farmacêutica
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