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Depression Quest HighEtiological diagnosis of pseudomembranous colitis.
In this study we compared the performances of various diagnostic methods in the detection of specific etiological causes of pseudomembranous colitis (PMC) (active and Crohn’s disease). One hundred and forty-eight patients with acute diarrhoea were studied. Eleven patients were affected with Crohn’s disease and 30 with PMC. A preliminary classification of all cases was carried out, based on the clinical picture, the results of different laboratory tests and the concurrent use of antibiotics. After diagnosis, subjects were allocated to a subgroup according to their clinical course or the presence of symptoms for at least 6 months. Clinical features and laboratory tests were studied in each group in order to provide a better understanding of the role of these methods in the detection of specific pathogens. The detection of H. pylori in the biopsies was the most valuable technique in the assessment of the etiology of this disease. The authors conclude that once there is a suspicion of Crohn’s disease, patients can be treated with antisecretory drugs or antibiotics, such as amoxycillin, metronidazole and tetracycline, which have a good therapeutic effect and prevent the development of complications.Synthesis and cytotoxic activities of 4-thiazolidinones as telomerase inhibitors.
A series of 4-thiazolidinone derivatives 4-22 were synthesized via hydrolytic kinetic study in DMSO with an intention to search new lead compounds for their anticancer activities. All the derivatives 4-22 containing carboxylic acid and alcohol groups (compounds 11, 12, 16, 17) showed cytotoxic activities in the nanomolar range against all tested cancer cell lines except for HepG2. The introduction of the ethyl ester group into C-4 position of 4-thiazolidinones (compounds 19, 22) resulted in losing the antitumor activity. The order of cytotoxic activity of the 4-thiazolidinones against the tested cancer cell lines was HepG2>A549>MCF-7>Hela>Hep3B>HT-29. Enzyme assays showed that the 4-thiazolidinones were strong inhibitors of
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