1980
DOI: 10.1136/gut.21.3.249
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Mucus and bicarbonate secretion in the stomach and their possible role in mucosal protection.

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Cited by 342 publications
(85 citation statements)
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“…Indeed, topical administration of 16,16-dimethyl PGE2 to resting canine gastric mucosa does cause vasodilatation (Cheung, 1980). Another possibility is that PGE2 averts mucosal damage through the stimulation of mucus and/or bicarbonate secretion (Allen & Garner, 1980). Topical application of PGE2 to the rat gastric mucosa does stimulate mucus production (Bolton, Palmer & Cohen, 1978), but as discussed above, there was no evidence in the present study that topical PGE2 caused luminal alkalinization.…”
Section: Discussioncontrasting
confidence: 53%
“…Indeed, topical administration of 16,16-dimethyl PGE2 to resting canine gastric mucosa does cause vasodilatation (Cheung, 1980). Another possibility is that PGE2 averts mucosal damage through the stimulation of mucus and/or bicarbonate secretion (Allen & Garner, 1980). Topical application of PGE2 to the rat gastric mucosa does stimulate mucus production (Bolton, Palmer & Cohen, 1978), but as discussed above, there was no evidence in the present study that topical PGE2 caused luminal alkalinization.…”
Section: Discussioncontrasting
confidence: 53%
“…Furthermore, the subcellular localization was essentially identical among the epithelial and glandular cells: the major site of localization was the basolateral or lateral membrane characterized by an aggregation of microvilli. Although physiological studies have demonstrated that the oxyntic, antral, and duodenal mucosae are capable of secreting HC03-under basal and stimulated conditions for cytoprotection against luminal gastric acid ( ALLEN and GARNER, 1980;KONTUREK et al, 1983), we failed to detect an intense immunoreactivity with OS-3 in the oxyntic mucosa of rats. The present immunohistochemical findings suggest that these HC03-secretory cells, except those in the oxyntic mucosa, have a common mechanism of HC03 production/secretion and that OS-3 recognizes a functional molecule involved in that mechanism.…”
Section: Substance Recognized By Os-3mentioning
confidence: 44%
“…In addition, the ability of anise suspension to protect gastric mucosa against lesions induced by chemical irritants is likely by maintaining the structural integrity of gastric epithelium and balance of aggressive factors and inherent protective mechanisms [52] . Further more, the mucus gel and its bicarbonate gradient seem to be an important first-line defense against harmful stimuli [53] .In conclusion, anise suspension exhibits an anti-ulcer potential activity through at least one or more possible mechanisms including inhibition of basal gastric secretion, stimulation of mucus secretion, endogenous gastric mucosal prostaglandin synthesis and possible antioxidative activity. …”
mentioning
confidence: 99%