Literature DB >> 6394242

Mucus glycoprotein structure, gel formation and gastrointestinal mucus function.

A Allen, D A Hutton, J P Pearson, L A Sellers.   

Abstract

Gastrointestinal mucus occurs as a water-insoluble gel adherent to the mucosal surfaces and as a viscous, mobile solution in the lumen. The adherent gastroduodenal mucus gel is part of the mucosal defence against acid (with HCO3-), pepsin (diffusion barrier) and mechanical damage. Rheological studies show that gastrointestinal mucus is a weak, viscoelastic gel. The size and physical properties of the isolated component glycoproteins depend critically on the methods used to obtain them. A glycoprotein preparation of Mr approximately 2 X 10(6), which possesses the gel-forming properties of the native mucus, is considered to represent the secreted covalent entity in pig gastric and small intestinal mucus. These glycoproteins have a polymeric structure of subunits joined by disulphide bridges between non-glycosylated regions of their protein cores. Glycoprotein polymerization, essential for gel formation, is deficient in gastric mucus in peptic ulcer disease. In vivo, adherent mucus gel forms a thin but continuous cover of variable thickness (rat 5-500 microns) over the gastroduodenal mucosa. Luminal pepsin rapidly dissolves this mucus cover and its continuity is maintained by fresh mucus secretion. Bile, HCl, 2 M-NaCl and ethanol (less than 40%) do not destroy mucus gel structure. Prostaglandins and carbachol increase mucus thickness, affording better protection, but it is thought that continuity of the protective mucus cover is the critical factor in its protective functions.

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Year:  1984        PMID: 6394242     DOI: 10.1002/9780470720905.ch10

Source DB:  PubMed          Journal:  Ciba Found Symp        ISSN: 0300-5208


  18 in total

1.  A separating method for quantifying mucus glycoprotein localized in the different layer of rat gastric mucosa.

Authors:  Y Komuro; K Ishihara; K Ishii; H Ota; T Katsuyama; K Saigenji; K Hotta
Journal:  Gastroenterol Jpn       Date:  1992-08

Review 2.  Mucus, pepsin, and peptic ulcer.

Authors:  C W Venables
Journal:  Gut       Date:  1986-03       Impact factor: 23.059

3.  Misoprostol-induced increases in adherent gastric mucus thickness and luminal mucus output.

Authors:  L A Sellers; N J Carroll; A Allen
Journal:  Dig Dis Sci       Date:  1986-02       Impact factor: 3.199

4.  Electron microscopy of cervical, gastric and bronchial mucus glycoproteins.

Authors:  J K Sheehan; K Oates; I Carlstedt
Journal:  Biochem J       Date:  1986-10-01       Impact factor: 3.857

Review 5.  Ameba-bacterium relationship in amebiasis.

Authors:  D Mirelman
Journal:  Microbiol Rev       Date:  1987-06

6.  Mucus gel thickness and turnover in the gastrointestinal tract of the rat: response to cholinergic stimulus and implication for mucoadhesion.

Authors:  A Rubinstein; B Tirosh
Journal:  Pharm Res       Date:  1994-06       Impact factor: 4.200

7.  Inhibition of attachment of Escherichia coli RDEC-1 to intestinal microvillus membranes by rabbit ileal mucus and mucin in vitro.

Authors:  B Drumm; A M Roberton; P M Sherman
Journal:  Infect Immun       Date:  1988-09       Impact factor: 3.441

8.  In vivo evaluation of an oral salmon calcitonin-delivery system based on a thiolated chitosan carrier matrix.

Authors:  Davide Guggi; Constantia E Kast; Andreas Bernkop-Schnürch
Journal:  Pharm Res       Date:  2003-12       Impact factor: 4.200

9.  Alternating laminated array of two types of mucin in the human gastric surface mucous layer.

Authors:  H Ota; T Katsuyama
Journal:  Histochem J       Date:  1992-02

10.  A new method of separation and quantitation of mucus glycoprotein in rat gastric mucus gel layer and its application to mucus secretion induced by 16,16-dimethyl PGE2.

Authors:  Y Komuro; K Ishihara; S Ohara; K Saigenji; K Hotta
Journal:  Gastroenterol Jpn       Date:  1991-10
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