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Métodos Terapêuticos e Terapias MTCI
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1.
Cancer Lett ; 157(1): 9-14, 2000 Aug 31.
Artigo em Inglês | MEDLINE | ID: mdl-10893436

RESUMO

The present study is part of a program to obtain effective chemopreventive agents with low toxicity from medicinal herbs and traditional herbal medicines. We previously reported that Oren (Coptidis rhizoma) and Ogon (Scutellariae radix) inhibit azoxymethane (AOM)-induced aberrant crypt foci (ACF) formation. In the present investigation, we found Sanshishi (Gardeniae fructus) and the traditional herbal medicine Oren-gedoku-to (OGT), composed of Ogon, Oren, Sanshishi and Obaku, also have preventive potential. Sanshishi and OGT decreased the numbers of ACF to 25.2 and 59.4% of the control value at 2% in the diet, respectively. Adverse effects, evidenced by body weight loss, were weaker with OGT than component herbs. To investigate their mechanisms of action, the influence on cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) activities was studied. Both OGT and Sanshishi inhibited COX-2 but not COX-1, this presumably contributing to their suppressive effects on ACF development. The results suggest that OGT may be useful for colon cancer chemoprevention in terms of efficacy and toxicity.


Assuntos
Anticarcinógenos/uso terapêutico , Neoplasias do Colo/prevenção & controle , Inibidores de Ciclo-Oxigenase/uso terapêutico , Medicamentos de Ervas Chinesas/uso terapêutico , Isoenzimas/antagonistas & inibidores , Lesões Pré-Cancerosas/prevenção & controle , Animais , Anticarcinógenos/toxicidade , Azoximetano/antagonistas & inibidores , Carcinógenos , Neoplasias do Colo/induzido quimicamente , Neoplasias do Colo/enzimologia , Ciclo-Oxigenase 1 , Ciclo-Oxigenase 2 , Inibidores de Ciclo-Oxigenase 2 , Inibidores de Ciclo-Oxigenase/toxicidade , Medicamentos de Ervas Chinesas/efeitos adversos , Isoenzimas/metabolismo , Masculino , Proteínas de Membrana , Extratos Vegetais/uso terapêutico , Extratos Vegetais/toxicidade , Lesões Pré-Cancerosas/induzido quimicamente , Lesões Pré-Cancerosas/enzimologia , Prostaglandina-Endoperóxido Sintases/metabolismo , Ratos , Ratos Endogâmicos F344
2.
Biol Pharm Bull ; 21(8): 814-7, 1998 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-9743248

RESUMO

This study was conducted to obtain effective cancer chemopreventive agents with low toxicity from medicinal herbs. The effect of aqueous extracts from 9 medicinal herbs with antiinflammatory effect were examined on the formation of azoxymethane (AOM)-induced aberrant crypt foci (ACF), putative preneoplastic lesions of the colon. Male F344 rats were treated with 15 mg/kg body weight of AOM once a week for two weeks. Herbal extract consisting of 2% of the diet was administered from 1 d prior to the first carcinogen treatment. The number of AOM-induced ACF per colon was counted at 4 week. Extracts of Coptidis Rhizoma and Scutellariae Radix significantly inhibited AOM-induced ACF formation. The number of ACF was decreased to 54% and 78% of that of the control by 2% Coptidis Rhizoma and Scutellariae Radix extract in the diet, respectively. Berberine and Baicalin, major ingredients of Coptidis Rhizoma and Scutellariae Radix, inhibited ACF formation at a dose equivalent to the amount in each herbal extract. Therefore, to investigate the mechanisms of action of berberine and baicalein which is the active substances of orally administered baicalin, their effects on cyclooxygenase 1 and 2 activities were studied. Berberine was found to inhibit cyclooxygenase 2 activity without inhibition of cyclooxygenase 1 activity, and baicalein inhibited cyclooxygenase 1 activity. Thus, Coptidis Rhizoma and Scutellariae Radix suppressed experimental colon carcinogenesis, and their chemopreventive effects were explained from the inhibition of berberine on cyclooxygenase 2 activity and baicalein on cyclooxygenase 1 activity.


Assuntos
Neoplasias do Colo/prevenção & controle , Plantas Medicinais , Lesões Pré-Cancerosas/prevenção & controle , Animais , Azoximetano , Berberina/farmacologia , Neoplasias do Colo/induzido quimicamente , Relação Dose-Resposta a Droga , Flavonoides/farmacologia , Masculino , Extratos Vegetais/farmacologia , Lesões Pré-Cancerosas/induzido quimicamente , Ratos , Ratos Endogâmicos F344
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