Intestinal absorption of aloe-emodin using single-passintestinal perfusion method in rat.
- Author:
Jinrong WANG
1
;
Ping WANG
;
Yongmao YANG
;
Xianli MENG
;
Yan ZHANG
Author Information
1. Chengdu University of Traditional Chinese Medicine, Chengdu 611730, China. 117978250@qq.com
- Publication Type:Journal Article
- MeSH:
Animals;
Anthraquinones;
pharmacokinetics;
Drugs, Chinese Herbal;
pharmacokinetics;
Female;
Humans;
Intestinal Absorption;
drug effects;
Intestines;
chemistry;
drug effects;
metabolism;
Male;
Perfusion;
methods;
Permeability;
Rats;
Rats, Sprague-Dawley
- From:
China Journal of Chinese Materia Medica
2011;36(17):2393-2398
- CountryChina
- Language:Chinese
-
Abstract:
The intestinal absorption of aloe-emodin was investigated using the single pass intestinal perfusion (SPIP) technique in S/D rats. SPIP was performed in each isolated segment of the intestine (i.e., duodenum, jejunum, ileum and colon) and the different concentrations inhibitor group of P-glycoprotein (P-gp) and multidrug resistance-associated protein (MRP2) with the concentrations of aloe-emodin (0.238 mg x L(-1)) at a flow rate of 0.28 mL x min(-1). The effective absorption rate constant (Ka) and apparent absorption coefficient (Papp) of aloe-emodin for each segment were determined before and after treated with different concentrations of inhibitors of P-gp and MRP2 respectively. Aloe-emodin exhibits a high intestinal permeability except the the ileum, indicative that the compounds are well absorbed. Decreases of Ka and Papp values in the duodenum, jejunum, colon and ileum, furthermore, the duodenum has significant increased compared with the ileum, there are have no significant difference in other isolated region of the intestine. Compared with the group which have no inhibitor of P-gp, the Ka and Papp were significantly increased in inhibitor of P-gp groups. Compared with the group of no inhibitor of MRP2, the Ka and Papp were significantly increased in inhibitor of MRP2 groups with the highest and the middle concentration. The results suggested that the inhibitors of P-gp and MRP2 all can promote the intestinal absorption of aloe-emodin.
