CHANGES IN RAT GASTRIC-MUCOSAL GLYCOPROTEINS IN PORTAL-HYPERTENSION

Citation
Jy. Wang et al., CHANGES IN RAT GASTRIC-MUCOSAL GLYCOPROTEINS IN PORTAL-HYPERTENSION, European surgical research, 29(4), 1997, pp. 280-286
Citations number
16
Categorie Soggetti
Surgery
Journal title
ISSN journal
0014312X
Volume
29
Issue
4
Year of publication
1997
Pages
280 - 286
Database
ISI
SICI code
0014-312X(1997)29:4<280:CIRGGI>2.0.ZU;2-M
Abstract
The aim of this study was to determine the effect of portal hypertensi on (PHT) on gastric mucosal glycoproteins in rats. PHT was induced exp erimentally by partial ligation of the portal vein (PVL) in 20 male Wi star rats: 10 rats (PVL4 group) were analyzed after 4 weeks and the re maining 10 (PVL8 group) after 8 weeks. In another group of 10 rats (co ntrol group), sham operations were performed. The severity of gastric mucosal lesions was evaluated macroscopically by a gross ulcer index. The gross ulcer indices in the PVL groups were significantly higher th an those in the controls (p < 0.05). Histomorphometric evaluation of t he intraepithelial mucin content, with the periodic acid-Schiff-Alcian blue staining technique, confirmed a significant decrease in mucosal glycoprotein production in the PVL groups (p < 0.05). Quantitative cha nges in gastric mucosal hexosamines were also used for mucosal glycopr otein analyses, and the hexosamine content of the gastric mucosa in th e control, PVL4 and PVL8 groups were 300.7 +/- 7.8, 177.2 +/- 4.9 and 169.1 +/- 3.5 mu g/100 mg dried mucosa, respectively. The gastric muco sal hexosamine content was significantly lower in the PVL groups than in the control group (p < 0.05). No significant differences were obser ved between the two PVL groups in the above-studied parameters. These findings reveal that PHT causes a decrease in gastric mucosal glycopro teins in rats, and the decreased mucin content may weaken an important defensive factor of gastric mucosa. We suggest that gastric mucosal g lycoproteins may play an important role in the pathogenesis of gastric mucosal lesions from PHT.