Absorption of flavonoids from Abelmoschus manihot extract by in situ intestinal perfusion.
- Author:
Cai-fu XUE
1
;
Jian-ming GUO
;
Da-wei QIAN
;
Jin-ao DUAN
;
Yan SHU
Author Information
1. Jiangsu Key Laboratory for Traditional Chinese Medicine Formulae Research, Nanjing University of Chinese Medicine, Nanjing 210046, China.
- Publication Type:Journal Article
- MeSH:
ATP Binding Cassette Transporter, Sub-Family B;
antagonists & inhibitors;
Abelmoschus;
chemistry;
Animals;
Flavonoids;
administration & dosage;
isolation & purification;
pharmacokinetics;
Flowers;
chemistry;
Intestinal Absorption;
drug effects;
Male;
Perfusion;
Plant Extracts;
chemistry;
Plants, Medicinal;
chemistry;
Quercetin;
administration & dosage;
analogs & derivatives;
isolation & purification;
pharmacokinetics;
Rats;
Rats, Sprague-Dawley;
Verapamil;
pharmacology
- From:
Acta Pharmaceutica Sinica
2011;46(4):454-459
- CountryChina
- Language:Chinese
-
Abstract:
To explore the mechanism of the absorption of flavonoids from Abelmoschus manihot flowers, in situ intestinal recirculation was performed to study the effect of the absorption at different concentrations and different intestinal regions. To evaluate the conditions of the absorption of six flavonoids from Abelmoschus manihot flowers, the concentrations of Abelmoschus manihot in the perfusion solution were determined by HPLC at predesigned time. And we have investigated the inhibitory effect of six flavonoids from Abelmoschus manihot flowers on P-glycoprotein (P-gp) drug efflux pump. The results demonstrated that the absorption rates of flavonoids from Abelmoschus manihot flowers are not significantly different (P > 0.05) at various drug concentrations, the absorption of flavonoids from Abelmoschus manihot flowers is a first-order process with the passive diffusion mechanism. The absorption rates of each of flavonoids are significantly different. The absorption rate of flavonoid glycoside was lower than that of aglycone; the flavonoids from Abelmoschus manihot flowers could be absorbed in all of the intestinal segments. The best parts of intestine to absorb hyperoside and myricetin are jejunum and duodenum, separately. Verapamil could enhance the absorption of isoquercitrin, hyperoside, myricetin and quercetin-3'-O-glucoside by inhibiting P-glycoprotein (P-gp) drug efflux pump.
