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Biomedical subjects

M Vasileva

Publications and source records attributed to M Vasileva.

At least 19 recordsLinked to original sources
PubMed1991

[Morphological changes in experimental duodenogastric reflux].

The model of a total duodenal-gastric reflux was developed in 20 dogs and morphological changes in the stomach were studied. 5 dogs served as control. Histologic changes occurred 3.5 months and 1 year after the operation were characterized by metachromasia, increased mucus formation, proliferation of epithelial and parietal cells, moderate inflammation. Process of the disease had fluctuations. 6 months after the operation 5 dogs were reoperated for the elimination of reflux and were observed for another 6 months. A complete reversibility of all changes was established. Bacteriological studies showed a considerable increase of bacteria population in the stomach and a pH increase. The authors suggest the term 'reflux gastropathy" to replace the term "alkaline reflux-gastritis".

Animals↗
PubMed1987

[Lyophilization of live CA-80 vaccine against coli enteritis in pigs].

A live vaccine against coli enteritis in pigs, CA-80, with a protection medium of 5 per cent hemodex, was successfully freeze-dried in ampoules or vials at the rate of 5 to 10 vaccinal doses each, the titer ranging from 10(9) to 10(10) live bacteria per cu. cm, of a 12-month shelf-life period. The vaccine was found to be innocuous for pigs, and was intended for active immunoprophylaxis on both infected and menaced farms and complexes, applying it to sows in the last third of the gestation period.

Animals↗
PubMed1984

Antagonistic effect of polyphloretin phosphate and di-4-phloretin phosphate on the contractile responses of guinea-pig gastric muscles to prostaglandin E2.

Polyphloretin phosphate (PPP) and di-4-phloretin phosphate (DPP) were studied for their ability to antagonize the contractions produced by prostaglandin E2 (PGE2) on isolated guinea-pig gastric muscles. PPP (100, 200 and 300 micrograms/ml) and DPP (10, 30 60 and 100 micrograms/ml) inhibited reversibly the PGE2-produced excitatory effect in longitudinal fundus and corpus muscles but did not influence the PGE2-produced inhibitory effect in circular muscle strips. In the presence of PPP and DPP the concentration-effect curves for PGE2 were shifted to the right parallel to control curves. The antagonistic action of PPP and DPP appeared to be a specific one since the compounds had little, if any, effect on the responses to histamine, acetylcholine and BaCL2. Analysis of the data (1) showed that DPP is a more potent antagonist than PPP against PGE2 on guinea-pig gastric muscle with pA2 6,1 and 4,8, respectively.

Animals↗