[The effects of taurine on oxidative processes in brain edema].

AIM: To investigate the free radical oxidation of lipids, oxidative modification of protein activity of glutathione peroxidase and glutathione reductase as well as the end product of nitric oxide - nitrite in the brain mitochondrial fraction of animals with experimentally induced cerebral edema and in treatment with taurine. MATERIAL AND METHODS: Toxic brain edema was induced in rats with intraperitoneal injection of tetra-ethyl lead (10 mg per kg of animal weight). The intensity of peroxidation was evaluated by hydroperoxide and malonic aldehyde contents. RESULTS: An analysis of the levels of oxidative modification of proteins revealed that brain edema was characterized by increased levels of oxidative modification of proteins and lipids, nitrogen oxide, reduced glutathione content and decrease in the activity of enzymes containing glutathione (glutathione peroxidase and glutathione reductase). CONCLUSION: On this basis, we suggested that drugs increasing glutathione content and activating enzymes containing glutathione, for example taurine, could be used as medications. The introduction of taurine in dose of 50 mg/kg during 5 days led to the reduction of lipid peroxidation products, normalization of oxidative modification of proteins in the mitochondrial fraction of the rats with experimental cerebral edema.

Quantitative analysis of phospholipids and gangliosides in bone marrow progenitors of lymphocytes, thymocytes and mature lymphocytes in tumor-bearing animals.

The phospholipid and ganglioside composition in bone marrow progenitors of lymphocytes, thymocytes and mature lymphocytes of intact rats and rats with sarcoma 45 were studied. The lymphocytes and their progenitors were isolated by Ficoll-Paque density centrifugation. The phospholipids and gangliosides were separated by thin-layer chromatography following standard chloroform:methanol extraction from the cells. Alterations in the lipid spectrum (both phospholipids and gangliosides) were shown to take place during lymphocyte differentiation. The rate of ganglioside sialylation diminished, which was expressed as an increase in mono- and di-, and a decrease in tri- and tetrasialoganglioside levels. Tumor-induced alterations in lymphocyte lipid composition involve all stages of lymphocyte differentiation. These shifts are believed to be connected with a disturbance of the antineoplastic function of lymphocytes and, consequently, the immune response of the tumor-bearing organism.