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Cod Mw2 Zone Ui Ff File.rar


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File Type: File Size: File Size: File Size: Code Previews for Your Projects We offer OCR-Aided Search and Efficient Bulk File Processing for small and large files. With a single click, you can check the image quality and preview every.pdf file.The stomach is the most important organ in maintaining the animal through which it extracts the proteins, carbohydrates and lipids to support the body. It is therefore no surprise that many drugs for the treatment of diseases, e.g., gastric ulcer and gastritis as well as inflammatory bowel disease, affect the stomach, by acting on its cells. Most of the current treatments that can be used to combat stomach disorders are based on the inhibition of gastric acid secretion, which can be either gastric acid secretion that normally occurs in the stomach or duodenal acid secretion that normally occurs in the duodenum and upper small intestine. The gastric acid inhibition can be generally divided into two groups: proton pump inhibitors (PPIs), which target the proton pump H+/K+ adenosine triphosphatase (H+/K+ ATPase) on the surface of the stomach cells and are represented by omeprazole (1), esomeprazole, lansoprazole, pantoprazole, rabeprazole and the like. The second group is H2 receptor antagonists, such as ranitidine (2), cimetidine (3), nizatidine and the like. The present invention relates to the use of certain selected bioactive agents that can be used to treat the above mentioned gastric disorders. One group of agents that has been proposed for use in the treatment of disorders of the stomach or duodenum are those that counteract the effects of bile acids. Thus, bile acids may be implicated in stomach disorders, for example, by playing a role in the pathogenesis of duodenal ulceration or gastric ulcers. The use of bile acid derivatives, e.g., ursodeoxycholic acid and glycine salt of chenodeoxycholic acid is disclosed in WO 01/75268, to reduce duodenal ulceration. It has also been proposed to administer bile acid derivatives to patients with gastric ulcer (WO 93/22000). Generally, bile acids are either steroidal molecules in which the carbon a2fa7ad3d0


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