Study on intestinal absorption features of oligosaccharides in Morinda officinalis How. with sigle-pass perfusion / 中国中药杂志
Zhongguo Zhong Yao Za Zhi
; (24): 134-140, 2015.
Article
in Zh
| WPRIM
| ID: wpr-305334
Responsible library:
WPRO
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.
Full text:
1
Index:
WPRIM
Main subject:
Oligosaccharides
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Perfusion
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Drugs, Chinese Herbal
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Pharmacokinetics
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Chemistry
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Rats, Sprague-Dawley
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Morinda
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Intestinal Absorption
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Intestine, Small
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Metabolism
Limits:
Animals
Language:
Zh
Journal:
Zhongguo Zhong Yao Za Zhi
Year:
2015
Type:
Article