Literature DB >> 10529087

Olestra formulation and the gastrointestinal tract.

R J Jandacek1, J J Kester, A J Papa, T J Wehmeier, P Y Lin.   

Abstract

Olestra is a mixture of compounds comprising sucrose esterified with 6-8 long-chain fatty acids. It is not hydrolyzed by pancreatic lipase and as a result is not absorbed from the small intestine. Olestra in general has physical properties similar to those of a triacylglycerol with the same fatty acid composition. Foods made with olestra are virtually identical in taste and texture to those made with typical triacylglycerols. Olestra consumption does not generate hydrolytic products in the small intestine and, therefore, does not generate some of the signals that alter motility in the gastrointestinal tract. A reduction in gastroesophageal reflux with olestra, in contrast to triacylglycerols, is consistent with a lack of effect on stomach emptying. Unlike triacylglycerols that are absorbed in the proximal small intestine, olestra is distributed throughout the small intestine during transit and passes into the colon. In the colon, olestra's effects depend on its physical properties. Liquid nondigestible lipids result in separation of oil from the fecal matrix. Olestra formulations made with specific fatty acid compositions, particularly those containing a solid sucrose polyester component including behenic acid, possess appropriate rheology to hinder separation of oil from the rest of the fecal matrix, thereby reducing gastrointestinal symptoms.

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Year:  1999        PMID: 10529087     DOI: 10.1007/s11745-999-0423-3

Source DB:  PubMed          Journal:  Lipids        ISSN: 0024-4201            Impact factor:   1.880


  34 in total

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Journal:  Fed Proc       Date:  1962 Jan-Feb

2.  Comparison of olestra absorption in guinea pigs with normal and compromised gastrointestinal tracts.

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Journal:  Fundam Appl Toxicol       Date:  1997-10

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Journal:  Am J Clin Nutr       Date:  1976-11       Impact factor: 7.045

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Authors:  D R Webb; G G Harrison; M J Lee; M H Huang
Journal:  J Nutr       Date:  1997-08       Impact factor: 4.798

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Journal:  Am J Physiol       Date:  1973-09

6.  A comparison of the effect of olestra and triglyceride on postprandial esophageal acid exposure.

Authors:  R Just; L Katz; M Verhille; T Schlagheck; D Castell
Journal:  Am J Gastroenterol       Date:  1993-10       Impact factor: 10.864

7.  Rate and extent of absorption of the fatty acids of fully esterified glycerol, erythritol, xylitol, and sucrose as measured in thoracic duct cannulated rats.

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Journal:  J Nutr       Date:  1972-09       Impact factor: 4.798

8.  Randomized, double-blind, placebo-controlled, consumer rechallenge test of Olean salted snacks.

Authors:  N L Zorich; D Biedermann; K A Riccardi; L J Bishop; T G Filloon
Journal:  Regul Toxicol Pharmacol       Date:  1997-10       Impact factor: 3.271

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Journal:  J Nutr       Date:  1980-10       Impact factor: 4.798

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Authors:  M A Eastwood; G S Allgood
Journal:  Eur J Clin Nutr       Date:  1995-09       Impact factor: 4.016

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  3 in total

1.  Authors' financial relationships with the food and beverage industry and their published positions on the fat substitute olestra.

Authors:  Jane Levine; Joan Dye Gussow; Diane Hastings; Amy Eccher
Journal:  Am J Public Health       Date:  2003-04       Impact factor: 9.308

Review 2.  Small bowel review: Normal physiology, part 1.

Authors:  Alan B R Thomson; Laurie Drozdowski; Claudiu Iordache; Ben K A Thomson; Severine Vermeire; M Tom Clandinin; Gary Wild
Journal:  Dig Dis Sci       Date:  2003-08       Impact factor: 3.199

3.  Design, Synthesis, and Testing of a Molecular Truck for Colonic Delivery of 5-Aminosalicylic Acid.

Authors:  Suryakiran Navath; Venkataramanarao Rao; Rita-Marie T Woodford; Monica T Midura-Kiela; Ali M Ahad; Ramesh Alleti; Pawel R Kiela; Eugene A Mash
Journal:  ACS Med Chem Lett       Date:  2012-08-01       Impact factor: 4.345

  3 in total

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