Literature DB >> 15055235

Interaction of bile salts with gastrointestinal mucins.

Timothy Scott Wiedmann1, Wei Liang, Heather Herrington.   

Abstract

The properties of three mucins were examined to identify the structural features responsible for their functional difterences. Bovine submaxillary mucin (BSM), porcine gastric mucin (PGM), and rat intestinal mucin (RIM) were each characterized, and high carbohydrate contents were found for RIM and PGM. The amino acid compositions were typical of mucin glycoproteins, with over half comprising small, neutral amino acids. Thereafter, each mucin was equilibrated with three different series of concentrations of the bile salts sodium taurocholate, sodium taurodeoxycholate, and sodium taurochenodeoxycholate. Following multiple centrifugations, the supernatant and mucin pellet concentrations of the bile salts were measured. The bile salt pellet concentration was plotted as a function of supernatant concentration, and from the slopes, the excluded volumes were calculated as 25, 29-44, and 28 55 mL/g for BSM, RIM, and PGM, respectively. The intercepts were 8-10, 2-3, and 1-3 mM for BSM, RIM, and PGM, respectively, which represents an estimate of the bound concentration of bile salt. Differences among the bile salts were observed in the excluded volume and amount bound, but no trends were evident. The bile salts may interact as aggregates with the hydrophobic areas and carbohydrate side chains of the mucins, providing favorable sites for association. The binding at low concentrations with exclusion at high concentrations is significant for modulating the absorption of lipid aggregates from the intestine. Finally, the differences among the mucins reflect the unique structure function relationship of these gastrointestinal mucins.

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Year:  2004        PMID: 15055235     DOI: 10.1007/s11745-004-1201-y

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


  21 in total

1.  Distribution and diffusion of sodium taurocholate and egg phosphatidylcholine aggregates in rat intestinal mucin.

Authors:  T S Wiedmann; H Herrington; C Deye; D Kallick
Journal:  Pharm Res       Date:  2001-11       Impact factor: 4.200

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Journal:  J Pharm Pharmacol       Date:  1990-07       Impact factor: 3.765

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Journal:  J Pharm Sci       Date:  1997-06       Impact factor: 3.534

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Authors:  A W Larhed; P Artursson; E Björk
Journal:  Pharm Res       Date:  1998-01       Impact factor: 4.200

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Journal:  Biochem Biophys Res Commun       Date:  1977-01-10       Impact factor: 3.575

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Journal:  Biochem Biophys Res Commun       Date:  1980-06-16       Impact factor: 3.575

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Journal:  Pharm Res       Date:  1996-04       Impact factor: 4.200

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Authors:  T Tsuji; T Osawa
Journal:  Carbohydr Res       Date:  1986-08-15       Impact factor: 2.104

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Journal:  Am J Physiol       Date:  1992-02

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Journal:  J Biol Chem       Date:  1984-10-10       Impact factor: 5.157

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  3 in total

1.  Pathophysiological basis of liver disease in cystic fibrosis employing a DeltaF508 mouse model.

Authors:  Folke Freudenberg; Annemarie L Broderick; Bian B Yu; Monika R Leonard; Jonathan N Glickman; Martin C Carey
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2008-04-24       Impact factor: 4.052

2.  Active transport of bile acids decreases mucin 2 in neonatal ileum: implications for development of necrotizing enterocolitis.

Authors:  Nina A Martin; Sarah K Mount Patrick; Teresa E Estrada; Harrison A Frisk; Daniel T Rogan; Bohuslav Dvorak; Melissa D Halpern
Journal:  PLoS One       Date:  2011-12-05       Impact factor: 3.240

3.  Bile Salts Modulate the Mucin-Activated Type VI Secretion System of Pandemic Vibrio cholerae.

Authors:  Verena Bachmann; Benjamin Kostiuk; Daniel Unterweger; Laura Diaz-Satizabal; Stephen Ogg; Stefan Pukatzki
Journal:  PLoS Negl Trop Dis       Date:  2015-08-28
  3 in total

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