Document Detail


Absorption of intestinal free cholesterol is lowered by supplementation of Areca catechu L. extract in rats.
MedLine Citation:
PMID:  12005171     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Areca extracts exhibiting a strong inhibitory activity against pancreatic cholesterol esterase (pCEase) in vitro were previously found to lower the absorption of dietary cholesteryl ester. Therefore, to determine whether a combined Areca extract also affects the absorption of intestinal free cholesterol, male rats were fed a diet containing free cholesterol (1%, w/w) either with or without an Areca nut extract supplement (0.5%, w/w). The Areca extract supplement significantly lowered the plasma cholesterol concentration by 25% without any change in the plasma triglyceride concentration, when compared to the control group. The supplement also significantly lowered the small intestinal pCEase activity by 39.1% compared to that of the control group. As regards the hepatic and intestinal ACAT activities, only the intestinal enzyme activity was significantly lowered by the supplement, when compared to the control group. The absorbed cholesterol that appeared in the blood after an oral dose of [1,2(n)-3H] free cholesterol was significantly lower in the rats supplemented with the Areca nut extract, compared with the control group. These results suggest that the inhibition of intestinal ACAT and possibly pCEase may facilitate the metabolic efficiency of the Areca nut extract as regards the absorption of intestinal free cholesterol. The structure and chemical properties of the active compound in the water-soluble Areca extract remain to be elucidated.
Authors:
Yong Bok Park; Seon-Min Jeon; Sung-June Byun; Hee-Sook Kim; Myung-Sook Choi
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Life sciences     Volume:  70     ISSN:  0024-3205     ISO Abbreviation:  Life Sci.     Publication Date:  2002 Mar 
Date Detail:
Created Date:  2002-05-13     Completed Date:  2002-05-29     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  0375521     Medline TA:  Life Sci     Country:  England    
Other Details:
Languages:  eng     Pagination:  1849-59     Citation Subset:  IM    
Affiliation:
Department of Genetic Engineering, Kyungpook National University, Taegu, South Korea.
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MeSH Terms
Descriptor/Qualifier:
Animals
Areca*
Cholesterol / metabolism*
Enzyme Inhibitors / pharmacology*
Intestinal Absorption / drug effects*
Male
Plant Extracts / pharmacology*
Rats
Rats, Sprague-Dawley
Sterol Esterase / antagonists & inhibitors*
Sterol O-Acyltransferase / antagonists & inhibitors*
Triglycerides / blood
Chemical
Reg. No./Substance:
0/Enzyme Inhibitors; 0/Plant Extracts; 0/Triglycerides; 57-88-5/Cholesterol; EC 2.3.1.26/Sterol O-Acyltransferase; EC 3.1.1.-/bile salt-stimulated lipase; EC 3.1.1.13/Sterol Esterase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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