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1.
Drug Metab Dispos ; 40(2): 381-8, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22086980

RESUMO

Rhizoma coptidis is a rhizome commonly used in traditional Chinese medicine. After oral administration of rhizoma coptidis extract, the plasma concentrations of its effective alkaloid constituents are so low that their systemic therapeutic actions cannot be explained. This study aimed to investigate the influence of lipopolysaccharide (LPS) on the pharmacokinetics of the rhizoma coptidis alkaloids. Pharmacokinetic experiments were performed with rats; both in vitro absorption and efflux experiments were carried out with everted rat gut sacs, whereas in vitro metabolism experiments were conducted with rat liver microsomes and intestinal S9 fractions. Mucosal changes were evaluated with light microscopy and transmission electron microscopy. The results showed that, in rat plasma, LPS pretreatment increased systemic alkaloid exposure. LPS pretreatment increased the in vitro absorption of the alkaloids and decreased their efflux. The efflux of vinblastine and rhodamine 123, P-glycoprotein substrates, also was decreased. The absorption of fluorescein isothiocyanate-labeled dextran (average molecular mass, 4 kDa), a gut paracellular permeability probe, was not influenced. Obvious damage was observed in the mucosa, but the tight junctions between epithelial cells remained intact. Intestinal, rather than hepatic, alkaloid metabolism was decreased. These findings indicated that LPS pretreatment increased systemic exposure to the alkaloids through enhancement of their absorption, which was related to decreased intestinal efflux and metabolism. The results add to the understanding of why rhizoma coptidis is active despite the low plasma concentrations of the rhizoma coptidis alkaloids measured in normal subjects and experimental animals.


Assuntos
Alcaloides/farmacocinética , Anti-Inflamatórios não Esteroides/farmacocinética , Medicamentos de Ervas Chinesas/farmacocinética , Íleo/metabolismo , Inflamação/metabolismo , Absorção Intestinal , Mucosa Intestinal/metabolismo , Alcaloides/sangue , Alcaloides/química , Alcaloides/metabolismo , Animais , Berberina/análogos & derivados , Berberina/análise , Berberina/sangue , Berberina/química , Berberina/metabolismo , Berberina/farmacocinética , Disponibilidade Biológica , Coptis chinensis , Medicamentos de Ervas Chinesas/química , Feminino , Glucuronídeos/metabolismo , Íleo/imunologia , Íleo/ultraestrutura , Inflamação/sangue , Inflamação/patologia , Mucosa Intestinal/imunologia , Mucosa Intestinal/ultraestrutura , Lipopolissacarídeos , Masculino , Microssomos Hepáticos/metabolismo , Distribuição Aleatória , Ratos , Ratos Sprague-Dawley
2.
J Ethnopharmacol ; 137(3): 1395-401, 2011 Oct 11.
Artigo em Inglês | MEDLINE | ID: mdl-21855623

RESUMO

ETHNOPHARMACOLOGICAL RELEVANCE: Rhizoma coptidis is a traditional Chinese medicine with pharmacological properties. It is usually prescribed with Fructus evodiae as traditional Chinese medicine (TCM) formulas. Here we report the influences of Fructus evodiae on the pharmacokinetics of the Rhizoma coptidis alkaloids and propose possible mechanisms. MATERIALS AND METHODS: Pharmacokinetic experiments were performed in rats. In vitro absorption experiments were performed in everted rat gut sacs, while in vitro metabolism experiments and determination of hepatic UDP-glucuronosyltransferase (UGT) 1A1 mRNA expression were performed in rat liver microsomes. RESULTS: Pretreatment with Fructus evodiae extract for two weeks decreased the systemic exposure of the Rhizoma coptidis alkaloids. This effect was not due to inhibition of absorption or enhanced hepatic phase I metabolism of the Rhizoma coptidis alkaloids. However, Fructus evodiae pretreatment enhanced both the activity and expression of hepatic UGT1A1. CONCLUSIONS: The results showed that Fructus evodiae pretreatment decreased the systemic exposure of the Rhizoma coptidis alkaloids by inducing hepatic UGT1A1.


Assuntos
Alcaloides/farmacocinética , Medicamentos de Ervas Chinesas/farmacocinética , Evodia , Mucosa Intestinal/metabolismo , Fígado/metabolismo , Ranunculaceae , Administração Oral , Alcaloides/administração & dosagem , Animais , Interações Medicamentosas , Medicamentos de Ervas Chinesas/administração & dosagem , Evodia/química , Feminino , Frutas , Glucuronosiltransferase/genética , Glucuronosiltransferase/metabolismo , Técnicas In Vitro , Absorção Intestinal , Fígado/efeitos dos fármacos , Masculino , Microssomos Hepáticos/metabolismo , Plantas Medicinais , Ranunculaceae/química , Ratos , Ratos Sprague-Dawley , Rizoma , Regulação para Cima
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