Related Experiment Video
Updated: Aug 7, 2026

Mouse- and Human-derived Primary Gastric Epithelial Monolayer Culture for the Study of Regeneration
Published on: May 7, 2018
Defense mechanisms of the gastric mucosa
Abstract:
The chemical and physical architecture of the apical membranes of the surface epithelial cells and of the tight junctions which bind the cells together, are such that water and water soluble substances are very slowly admitted. This impermeability is the most important factor in the defense of the gastric mucosa against damaging agents. The barrier provided by this impermeability can be measured by determining the rate of passage of substances from gastric contents to blood. Damage to the barrier will be reflected in an increase in this rate. The common ions, H+, Na+, K+, Cl- and HCO3- and water provide suitable yardsticks for the estimate. The rate of entry of H+ is the most important for it is the common agent producing serious damage to mucosal cells. The state of the barrier is not static. It can be lowered or raised. Barrier breakers are fat soluble, e.g. ethanol, bile, aspirin. They enter the apical membranes of the surface epithelial cells and in doing so permit H+ and other ions to penetrate at accelerated rates. Exposure to a damaging agent can, however, produce an increase in the resistance of the mucosa to subsequent exposures. Increased resistance of the mucosa can be accomplished also by pretreatment with prostaglandins or epidermal growth factor. Both inhibit acid secretion and this is an important element in limiting mucosal damage. Prostaglandins and some barrier breakers also increase the production of HCO3- and of mucus by the mucosa. Both may aid in disposal of damaging agents. Increases in mucosal circulation can also contribute by ridding the submucosa of damaging substances. Protective factors can also increase the impermeability of the membrane but how this is accomplished is unknown.
More Related Videos
Related Concept Videos
Pathophysiology of Peptic Ulcer Disease: Injurious Factors
In the antrum region, G cells secrete the gastrin hormone that binds to gastrin-cholecystokinin-B (CCK2) receptors on parietal and enterochromaffin-like (ECL) cells in the fundic glands. Simultaneously, the vagus nerve releases acetylcholine, which binds to M3...
Pathophysiology of Peptic Ulcer Disease: Mucosal Defense Factors
Drugs for Peptic Ulcer Disease: Sucralfate as Mucosal Protective Agents
In this scenario, mucosal protective agents like sucralfate play an essential role. Sucralfate, a complex of sulfated sucrose and aluminum hydroxide, demonstrates its usefulness in acidic conditions,...
Mucosal Barrier of the Stomach
Within parietal cells, carbonic acid is first formed through the reaction of water and carbon dioxide. The dissociation of carbonic acid releases bicarbonate and hydrogen ions. The bicarbonate...
Peptic Ulcer Disease II: Pathophysiology
Damaging agents such as Helicobacter pylori, gastric acid, pepsin, and nonsteroidal anti-inflammatory drugs (NSAIDs) can weaken the mucosal defense, allowing hydrogen ions to infiltrate back and harm epithelial cells.
Peptic Ulcer Disease II: Pathophysiology

