Literature DB >> 25232384

Aripiprazole an atypical antipsychotic protects against ethanol induced gastric ulcers in rats.

Abdulrahman Al Asmari1, Mohammed Arshaduddin1, Ibrahim Elfaki1, Saeed Kadasah2, Abdulrahman Al Robayan3, Saeed Al Asmary4.   

Abstract

The present investigation was undertaken, to study the gastro-protective potential of aripiprazole (ARI) an atypical antipsychotic drug in ethanol induced gastric ulcers in rats. ARI (10, 30, 100 mg/kg) was tested for gastric secretion and antiulcer activity in different groups of male Sprague Dawley rats. Gastric secretion and acidity studies were performed in pylorus ligated rats while indices of gastric ulcers were measured in ethanol (1 ml-100%) induced gastric ulcers. Histological changes and the levels of gastric wall mucus, malondialdehyde (MDA), non-protein sulfhydryls (NP-SH), myeloperoxidase (MPO), and serotonin were used to assess ethanol induced gastric mucosal injuries. Exposure of rats to ethanol resulted in gastric mucosal injury and a high index of ulcer. Pretreatment with ARI significantly (P < 0.001), reduced the gastric lesions induced by ethanol and also resulted in a significant decrease in the gastric secretion, and total acidity in pylorus ligated rats. ARI also significantly attenuated the ethanol induced reduction in the levels of gastric wall mucus, and NP-SH (P < 0.001). The histological changes and the increased MDA and MPO activity were also significantly (P < 0.001) inhibited by ARI. Ethanol induced depletion in the levels of serotonin in the gastric tissue were also significantly restored by pretreatment with ARI (p < 0.001). ARI showed significant antiulcer and gastroprotective activity against ethanol induced gastric ulcers. The gastroprotective effects of ARI may be due to its anti-secretory, antioxidant and anti-inflammatory action and also due to the restoration of the depleted gastric serotonin levels.

Entities:  

Keywords:  Gastric ulcer; aripiprazole; dopamine; ethanol; myeloperoxidase; oxidative stress; serotonin

Year:  2014        PMID: 25232384      PMCID: PMC4161544     

Source DB:  PubMed          Journal:  Int J Clin Exp Med        ISSN: 1940-5901


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