[Change of the reactibility of the myocardium following the termination of the beta-blocking effect of trimepranol and practolol].
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Biomedical subjects
Publications and source records attributed to P Svec.
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The effect of N-(2-hydroxyethyl)-palmitamide (PEA), an active endogenous compound, which may be useful in preventing virus infections of the respiratory tract, was studied in chicken sarcoma RBA-34 and mouse Rauscher leukemia. The experiments showed that PEA did not influence the induction, development and severity of experimental oncogenic diseases investigated.
The effects of N-(2-hydroxyethyl) palmitamide (PEA) a natural and antitoxic substance on the treatment of RBA rat leukemia were studied. Repeated administration of PEA prolonged substantially survival of leukemic animals in the course of the treatment with cis-diamminedichlor-platinum (cis-Pt(II) in combination with cyclophosphamide, vincristine and methotrexate respectively. The most advantageous combination used was the cis-Pt(II) with methotrexate and PEA administration even improved the treatment results. The long-termed PEA treatment depressed first of all undesirable side effects and enabled to use higher therapeutic dosage of chemotherapeutics and improved the final results.
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1. Histamine release by antigen from three sensitized rat tissues is potentiated by phosphatidyl serine (PS). The effect is greatest with isolated peritoneal cells. Phosphatidyl inositol, ethanolamine, choline and phosphatidic acid are inactive.2. PS greatly increases the rate of antigen-induced histamine release and only slightly prolongs the duration of the release process.3. PS shows a concentration-dependent effect over the range 1-10 mug/ml. At 10 mug/ml it is active over a wide range of antigen concentrations.4. Calcium ions are necessary for the potentiation by PS of antigen-induced histamine release from rat peritoneal cells.
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