Topical and intravenous administration of trefoil factors protect the gastric mucosa from ethanol-induced injury in the rat

被引:27
作者
McKenzie, C
Thim, L
Parsons, ME
机构
[1] Univ Hertfordshire, Biosci Div, Gastrointestinal Pharmacol Unit, Hatfield AL10 9AB, Herts, England
[2] Novo Nordisk AS, Bagsvaerd, Denmark
关键词
D O I
10.1046/j.1365-2036.2000.00796.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: hTFF2 and pTFF2 (formerly PSP and hSP, respectively) are members of the trefoil factor family (TFF) and are distributed throughout the gastrointestinal tract in both normal and diseased tissue. Trefoil factors have been shown to exert a mucosal protectant and/or healing role in a number of animal models but controversy exists surrounding this property in relation to their dose and route of administration. Aim: To investigate the effects of topically applied and intravenously infused trefoil factors (hTFF2 and pTFF2) and prostaglandin E-2 On ethanol-induced gastric mucosal damage in rats. Method: A gastric chamber preparation in the anaesthetized rat was used, Injury was caused by exposing the gastric mucosa to absolute ethanol for 1 min. Trefoil factors or prostaglandin E-2 were administered either intravenously or topically before and after the introduction of absolute ethanol onto the gastric mucosa. Damage was assessed by measurement of gastric mucosal Na+ leakage and area of macroscopic injury, Results: Like prostaglandin E-2, intravenous administration of hTEF2 and pTFF2 reduced both the gastric mucosal Na+ leakage and the mean area of damage caused by ethanol, Similarly, treatment of the gastric mucosa with topical application of hTFF2 at doses of 120 mu g/kg and above reduced the Na+ leakage and the area of damage. pTFF2 at 120 mu g/kg and 1.2 mg/kg applied topically produced a marked reduction in total area of damage. Conclusion: Intravenously infused hTFF2 and pTFF2 protect the gastric mucosa from ethanol-induced damage in the anaesthetized rat. In addition, topical application of trefoil factors also was effective at protecting the gastric mucosa from injury at doses lower than previously reported.
引用
收藏
页码:1033 / 1040
页数:8
相关论文
共 26 条
[1]   Oral trefoil peptides protect against ethanol- and indomethacin-induced gastric injury in rats [J].
Babyatsky, MW ;
deBeaumont, M ;
Thim, L ;
Podolsky, DK .
GASTROENTEROLOGY, 1996, 110 (02) :489-497
[2]   COMBINED INTESTINAL TREFOIL FACTOR AND EPIDERMAL GROWTH-FACTOR IS PROPHYLACTIC AGAINST INDOMETHACIN-INDUCED GASTRIC DAMAGE IN THE RAT [J].
CHINERY, R ;
PLAYFORD, RJ .
CLINICAL SCIENCE, 1995, 88 (04) :401-403
[3]   TREFOIL PEPTIDES PROMOTE EPITHELIAL MIGRATION THROUGH A TRANSFORMING GROWTH-FACTOR BETA-INDEPENDENT PATHWAY [J].
DIGNASS, A ;
LYNCHDEVANEY, K ;
KINDON, H ;
THIM, L ;
PODOLSKY, DK .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (01) :376-383
[4]  
HARDING PL, 1981, THESIS QUEENS U KING
[5]  
ITO S, 1984, MECHANISMS MUCOSAL P, P57
[6]   SPASMOLYTIC POLYPEPTIDE - A TREFOIL PEPTIDE SECRETED BY RAT GASTRIC MUCOUS CELLS [J].
JEFFREY, GP ;
OATES, PS ;
WANG, TC ;
BABYATSKY, MW ;
BRAND, SJ .
GASTROENTEROLOGY, 1994, 106 (02) :336-345
[7]   PANCREATIC SPASMOLYTIC POLYPEPTIDE (PSP) .1. PREPARATION AND INITIAL CHEMICAL CHARACTERIZATION OF A NEW POLYPEPTIDE FROM PORCINE PANCREAS [J].
JORGENSEN, KH ;
THIM, L ;
JACOBSEN, HE .
REGULATORY PEPTIDES, 1982, 3 (3-4) :207-219
[8]   TREFOIL PEPTIDE PROTECTION OF INTESTINAL EPITHELIAL BARRIER FUNCTION - COOPERATIVE INTERACTION WITH MUCIN GLYCOPROTEIN [J].
KINDON, H ;
POTHOULAKIS, C ;
THIM, L ;
LYNCHDEVANEY, G ;
PODOLSKY, DK .
GASTROENTEROLOGY, 1995, 109 (02) :516-523
[9]  
KONTUREK SJ, 1981, GASTROENTEROLOGY, V81, P438
[10]   ENDOGENOUS GASTRIC-MUCOSAL PROSTAGLANDINS - THEIR ROLE IN MUCOSAL INTEGRITY [J].
LIGUMSKY, M ;
GROSSMAN, MI ;
KAUFFMAN, GL .
AMERICAN JOURNAL OF PHYSIOLOGY, 1982, 242 (04) :G337-G341