Effects of ecabet sodium on acute mixed reflux esophagitis in rats.

Abstract

OBJECTIVE: Ecabet sodium (ENa) is a drug that repairs epithelial cells in the digestive tract via selective adhesion to damaged tissue. While the principal cause of reflux esophagitis is gastroesophageal acid reflux, the involvement of duodenal juice has also been identified as an important factor. This study aimed to explore the effect of ENa in an acute mixed reflux esophagitis (AMRE) rat model. MATERIAL AND METHODS: Eight-week-old male Wistar rats were used to prepare an AMRE model. There were four experimental groups: Group A (sham-operated rats), Group B (AMRE rats), Group C (AMRE rats dosed with ENa at 10 mg/kg), and Group D (AMRE rats dosed with ENa at 30 mg/kg). All rats were assessed for incidence of macroscopic esophageal lesions, esophagitis index, and pathological findings. Amylase activity, bile acid concentration in the digestive fluid retained in the esophagogastric lumen and ENa concentration in the esophageal mucosa were determined. RESULTS: The incidence of esophagitis was 0% for Group A, 100% for Group B, 40% for Group C, and 20% for Group D. It was significantly lower for Groups C and D relative to Group B. The median esophagitis index was 0 for Group A, 58.2 for Group B, 0 for Group C, and 0 for Group D, and it was significantly lower for Groups C and D relative to Group B. The histological severity grade of esophagitis in Groups C and D was significantly less than that in Group B. CONCLUSION: Treatment with ENa inhibited the development of AMRE in rats.