Subject(s)
Antineoplastic Agents/pharmacology , Brain Neoplasms/drug therapy , Caffeine/analogs & derivatives , Animals , Antineoplastic Agents/therapeutic use , Blood-Brain Barrier , Brain Neoplasms/metabolism , Caffeine/metabolism , Caffeine/pharmacology , Caffeine/therapeutic use , DNA Repair/drug effects , Humans , Radiation-Sensitizing Agents/pharmacologyABSTRACT
In experiments on rats (290 animals) exposed to chronic gamma-radiation with the total dose of 10.0 Gy it was detected that prescription of synthetic pharmaceutical of the dihydropyridine class--glutapyrone--together with drinking water during 6 months reduced the rate of malignant neoplasms from 26.5% in the control group to 13% in the treated animals. In radiation-exposed rats that received glutapyrone there was a narrowing of spectrum of the emerged neoplasms (connectively-tissual tumors only) as compared to the animals of the radiated control group, where blastomas of epithelium and lymphoid origin were also revealed. Low toxicity of glutapyrone and its anticarcinogenic action show the potential for this preparation to be used in practice.
Subject(s)
Anticarcinogenic Agents/pharmacology , Dihydropyridines/pharmacology , Gamma Rays , Glutamates/pharmacology , Neoplasms, Radiation-Induced/prevention & control , Administration, Oral , Animals , Anticarcinogenic Agents/administration & dosage , Dihydropyridines/administration & dosage , Female , Glutamates/administration & dosage , Hematologic Neoplasms/etiology , Hematologic Neoplasms/prevention & control , Neoplasms, Glandular and Epithelial/etiology , Neoplasms, Glandular and Epithelial/prevention & control , Neoplasms, Radiation-Induced/etiology , RatsABSTRACT
The paper presents data on the effect of 5-fluorouracil (5-FU)-impregnated Coletex napkins on rats and mice with transplantable subcutaneous tumors of different histological patterns: Pliss lymphosarcoma, Walker carcinosarcoma and Ehrlich carcinoma. Since the napkins showed antitumor activity it is suggested that they might find application in treating a number of oncological pathologies, particularly, skin lesions and ulcerated and necrotized tumors.
Subject(s)
Antimetabolites, Antineoplastic/therapeutic use , Carcinoma, Ehrlich Tumor/drug therapy , Fluorouracil/therapeutic use , Administration, Cutaneous , Animals , Antimetabolites, Antineoplastic/administration & dosage , Carcinoma, Ehrlich Tumor/pathology , Female , Fluorouracil/administration & dosage , Male , Mice , RatsABSTRACT
In experiments with mice subjected to whole-body X-irradiation a radioprotective effect of riboxine (inosine) was demonstrated. The observed effect may be attributed to the ability of the preparation to interfere with the cyclic nucleotide metabolism.
Subject(s)
Inosine/therapeutic use , Radiation Injuries, Experimental/prevention & control , Radiation-Protective Agents/therapeutic use , Animals , Mice , Whole-Body IrradiationABSTRACT
In experiments on mice with solid sarcoma 37, a study was made of modification of the radiosensitizing effect of metronidazole. The increase in the leucotic interferon titre, induced by the interferon synthesis inductors, did not influence the radiosensitizing efficiency of metronidazole: after the administration of the repair inhibitor, 8-bromocaffeine, the coefficient of suppression of tumor growth was higher and the number of mice with the regressed tumors greater as compared to animals affected by metronidazole and radiation.
Subject(s)
Caffeine/analogs & derivatives , Interferon Inducers/therapeutic use , Metronidazole/therapeutic use , Radiation-Sensitizing Agents , Sarcoma 37/radiotherapy , Sarcoma, Experimental/radiotherapy , Animals , Caffeine/administration & dosage , Caffeine/therapeutic use , DNA Repair/drug effects , Drug Synergism , Interferon Inducers/administration & dosage , Metronidazole/administration & dosage , Mice , Mice, Inbred StrainsABSTRACT
Among newly synthesized purine compounds there are drugs that are capable to increase the leukocyte count in the peripheral blood of irradiated animals. The derivatives of xanthine and adenine under study were marked by low toxicity.
Subject(s)
Hematopoiesis/drug effects , Leukocytes/physiology , Purines/therapeutic use , Radiation Injuries, Experimental/drug therapy , Animals , Mice , Stimulation, ChemicalSubject(s)
Caffeine/analogs & derivatives , Hematopoietic Stem Cells/radiation effects , Radiation Injuries, Experimental/blood , Animals , Caffeine/therapeutic use , Cell Survival/drug effects , Cell Survival/radiation effects , Female , Mice , Radiation Dosage , Radiation Injuries, Experimental/prevention & control , Radiation ToleranceSubject(s)
Caffeine/analogs & derivatives , Hematopoietic Stem Cells/drug effects , Radiation-Sensitizing Agents/pharmacology , Animals , Caffeine/pharmacology , Colony-Forming Units Assay , Dose-Response Relationship, Radiation , Hematopoietic Stem Cells/radiation effects , Male , Mice , Mice, Inbred C57BL , Mice, Inbred CBAABSTRACT
Effects of 8-bromoadenine have been investigated on the prereplicative and post-replicative processes of DNA repair in gamma-irradiated monolayer HeLa-M cells, a method of ultracentrifugation in alkaline sucrose gradients being used. A 30-90 minutes treatment of cells with 8-bromoadenine before irradiation (1, 5, 20 krad) distinctly inhibits the DNA single-strand break repair. The molecular weight of DNA, synthesized in gamma-irradiated cells in the presence of 8-bromoadenine, is less than that synthesized without 8-bromoadenine.