Study on intestinal absorption features of oligosaccharides in Morinda officinalis How. with sigle-pass perfusion.
- Author:
Shao-Dong DENG
;
Peng ZHANG
;
Li LIN
;
Feng-Xia XIAO
;
Jing-Ran LIN
- Publication Type:Journal Article
- MeSH:
Animals;
Drugs, Chinese Herbal;
chemistry;
pharmacokinetics;
Intestinal Absorption;
Intestine, Small;
metabolism;
Male;
Morinda;
chemistry;
Oligosaccharides;
chemistry;
pharmacokinetics;
Perfusion;
Rats;
Rats, Sprague-Dawley
- From:
China Journal of Chinese Materia Medica
2015;40(1):134-140
- CountryChina
- Language:Chinese
-
Abstract:
To study the in situ intestinal absorption of five oligosaccharides contained in Morinda officinalis How. (sucrose, kestose, nystose, 1F-Fructofuranosyinystose and Bajijiasu). The absorption of the five oligosaccharides in small intestine (duodenum, jejunum and ileum) and colon of rats and their contents were investigated by using in situ single-pass perfusion model and HPLC-ELSD. The effects of drug concentration, pH in perfusate and P-glycoprotein inhibitor on the intestinal absorption were investigated to define the intestinal absorption mechanism of the five oligosaccharides in rats. According to the results, all of the five oligosaccharides were absorbed in the whole intestine, and their absorption rates were affected by the pH of the perfusion solution, drug concentration and intestinal segments. Verapamil Hydrochloride could significantly increase the absorptive amount of sucrose and Bajijiasu, suggesting sucrose and Bajijiasu are P-gp's substrate. The five oligosaccharides are absorbed mainly through passive diffusion in the intestinal segments, without saturated absorption. They are absorbed well in all intestines and mainly in duodenum and jejunum.
