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Endothelin and neonatal capsaicin regulate gastric resistance to injury in BDL rats
Authors:Paula RS C&#  mara  Gerson JN Ferraz  Licio A Velloso  José  Murilo R Zeitune  Fernando AB Suassuna  Jose Geraldo P Ferraz
Affiliation:Paula RS Câmara, Fernando AB Suassuna, Department of Medicine, Potiguar University, RN 59056-000, BrazilPaula RS Câmara, Gerson JN Ferraz, Licio A Velloso, José Murilo R Zeitune, Jose Geraldo P Ferraz, GI Research Lab, Gastrocentro, Department of Medicine, Faculty of Medical Sciences, University of Campinas, SP 13083-878, BrazilJose Geraldo P Ferraz, Division of Gastroenterology, Faculty of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada
Abstract:AIM: To investigate the relationship between primary afferent neurons, endothelin (ET) and the role of its receptors on ethanol-induced gastric damage in cirrhotic rats. METHODS: Cirrhosis and portal hypertension were induced in rats by bile duct ligation (BDL) while controls had a sham operation. The association between ET and afferent neurons on the gastric mucosa was evaluated by capsaicin treatment in newborn rats, the use of ET agonists or antagonists, gastric ET-1 and -3 mRNA and synthetic capacity. Ethanol-induced damage was assessed using ex vivo gastric chamber experiments.Gastric blood flow was measured by laser-Doppler flow-metry. RESULTS: ET-3 and an ETB receptor antagonist sig- nificantly reduced the extent of ethanol-induced gastric damage in BDL rats. Gastric ET-1 and -3 levels were 30% higher in BDL rats compared to control rats. Cap-saicin treatment restored the gastric resistance and blood flow responses to topical application of ethanol in BDL rats and ET-1 and -3 production to levels observed in controls. CONCLUSION: Our results suggest that the reduced resistance of the gastric mucosa of cirrhotic rats to ethanol-induced injury is a phenomenon modulated by ET through the ET B receptor and by sensory afferent neurons.
Keywords:Endothelins   Tachykinins   Portal hypertension   Gastropathy   Cirrhosis
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