Role of pectins in the complex treatment in patients in neurointensive care units]

Clinical and laboratory estimation of the efficacy of pectins in complex treatment of patients with intracranial hematoma was performed. It was shown that in the group of the patients treated with pectins vs the control group development of pyo-inflammatory infections was less frequent, the indices of the immunity status improved and a more rapid decrease of the intoxication and a more rapid normalization of the composition of various biotopes in the patients were observed.     

Self-assembly of soluble unlinked and cross-linked fibrin oligomers

Self-assembly of soluble unlinked and cross-linked fibrin oligomers formed from desA-fibrin monomer under the influence of factor XIIIa was studied in the presence of non-denaturing urea concentrations. By methods of elastic and dynamic light scattering combined with analytical ultracentrifugation, desA-fibrin oligomers formed in both the presence and absence of the factor XIIIa were shown to be ensembles consisting of soluble rod-like double-stranded protofibrils with diverse weight and size. Unlinked and cross-linked soluble double-stranded protofibrils can reach the length of 350–450 nm. The structure of soluble covalently-linked protofibrils is stabilized by isopeptide γ-dimers. Electrophoretic data indicate a complete absence of isopeptide bonds between α-chains of desA-fibrin molecules. The molecular mechanism of formation of soluble rod-like fibrin structures and specific features of its covalent stabilization under the influence of factor XIIIa are discussed.     

Inhibition of exocytosis or endocytosis blocks activity-dependent redistribution of synapsin

The synaptic vesicle cycle encompasses the pre-synaptic events that drive neurotransmission. Influx of calcium leads to the fusion of synaptic vesicles with the plasma membrane and the release of neurotransmitter, closely followed by endocytosis. Vacated release sites are repopulated with vesicles which are then primed for release. When activity is intense, reserve vesicles may be mobilized to counteract an eventual decline in transmission. Recently, interplay between endocytosis and repopulation of the readily releasable pool of vesicles has been identified. In this study, we show that exo-endocytosis is necessary to enable detachment of synapsin from reserve pool vesicles during synaptic activity. We report that blockage of exocytosis in cultured mouse hippocampal neurons, either by tetanus toxin or by the deletion of munc13, inhibits the activity-dependent redistribution of synapsin from the pre-synaptic terminal into the axon. Likewise, perturbation of endocytosis with dynasore or by a dynamin dominant-negative mutant fully prevents synapsin redistribution. Such inhibition of synapsin redistribution occurred despite the efficient phosphorylation of synapsin at its protein kinase A/CaMKI site, indicating that disengagement of synapsin from the vesicles requires exocytosis and endocytosis in addition to phosphorylation. Our results therefore reveal hitherto unidentified feedback within the synaptic vesicle cycle involving the synapsin-managed reserve pool.     

Interrelations of mitochondrial fragmentation and cell death under ischemia/reoxygenation and UV-irradiation: protective effects of SkQ1, lithium ions and insulin

Mitochondria-targeted antioxidant 10-(6-plastoquinonyl)decyltriphenyl-phosphonium (SkQ1) as well as insulin and the inhibitor of glycogen-synthase kinase, Li(+) are shown to (i) protect renal tubular cells from an apoptotic death and (ii) diminish mitochondrial fission (the thread-grain transition) induced by ischemia/reoxygenation. However, SkQ1 and LiCl protected the mitochondrial reticulum of skin fibroblasts from ultraviolet-induced fission but were ineffective in preventing a further cell death. This means that mitochondrial fission is not essential for apoptotic cascade progression.     

Taxonomic revision of Tatria Kowalewski, 1904 (Cestoda: Amabiliidae): redescriptions of T. biremis Kowalewski, 1904 and T. minor Kowalewski, 1904, and the description of T. gulyaevi n. sp. from Palaearctic grebes

Two species of Tatria Kowalewski, 1904 are redescribed from grebes in Bulgaria: T. biremis Kowalewski, 1904 (specimens from Podiceps nigricollis) and T. minor Kowalewski, 1904 (specimens from P. cristatus and P. nigricollis). T. mircia Gulyaev, 1990 is synonymised with T. minor. The previous records of T. biremis, T. minor and T. mircia are critically analysed in view of the present results. T. gulyaevi n. sp. is described from P. nigricollis from Bulgaria and the Czech Republic and from an unidentified grebe species from Turkey. Some of the previous records of T. minor and T. biremis are recognised as belonging to T. gulyaevi. One specimen illustrated by Kowalewski (1904) is designated as a lectotype of T. minor in order to stabilise the nomenclatural standing of this species.     

Significance of NOTCH1 Expression in the Progression of Human Lung and Colorectal Cancers

Biochemistry (Moscow) - Lung and colorectal cancers are the most common types of cancer characterized by a poor prognosis and a high mortality rate. Mutations in the genes encoding components of...     

Nutritive value of forage biomass from sainfoin mixtures

Forage quality characteristics of field-grown mixtures of sainfoin with cocksfoot (50:50%), sainfoin with tall fescue (50:50%), and the same with the addition of subterranean clover in their composition (33:33:33%) were measured. Forage biomass from the mixtures of sainfoin with cocksfoot had generally higher forage quality than mixtures with tall fescue. It had higher crude protein content (11.52% of dry matter (with 1.07% units), significantly higher digestibility (61.74%) (with 6.51% units), higher neutral detergent fiber content (53.42%) (with 3.22% units), higher nutritive value (Unité Fourragère Viande – Unité Fourragère Lait, 0.690–0.583) and higher protein feeding value (Total Digestible Protein – Protein digestible dans l’intestine in dependence of nitrogen – Protein digestible dans l’intestine in dependence of energy), 72–70–79 g/kg of dry matter. Forage biomass showed more balanced basic chemical composition after the addition of subterranean clover, i.e.: higher crude protein content (with 0.30% units) and lower crude fiber content (with 0.14% units) for mixtures with cocksfoot; higher digestibility (with 0.29% units) for mixtures with cocksfoot; lower neutral detergent fiber content (with 0.45% units) for mixtures with cocksfoot and with 3.15% units for mixtures with tall fescue, higher energy feeding value (Unité Fourragère Viande – Unité Fourragère Lait) (with 0.007–0.012 for mixtures with cocksfoot and with 0.009–0.014 for mixtures with tall fescue), higher protein feeding value for both mixtures with cocksfoot and tall fescue. Forage biomass from mixtures of sainfoin with cocksfoot and Trifolium subterraneum ssp. brachycalicinum had the highest crude protein (11.89% of dry matter), the lowest crude fiber content (27.07% of dry matter) and the highest digestibility (62.81% of dry matter).     

Cultivation of boar spermatogonia on Sertoli cells

We studied the in vitro effect of Sertoli cells on boar spermatogonia isolated from the testes of 60-day-old crossbred boars. In order to enrich the culture with spermatogonia, the cells were purified by density gradient centrifugation with the use of Percoll gradient followed by separation based on adhesive capacities of cells. We found lipid drops stained by Oil Red O in Sertoli cells. The experiments showed that the cultivation of boar spermatogonia in the presence of Sertoli cells (for up to 35 days) provide the same way of differentiation as in testes in natural conditions. After 10 days of cultivation, spermatogenic cells form groups, chains, and suspension clusters. By this time, spermatogenic colonies are formed; we analyzed the expression of Nanog and Plzf genes in these colonies by real-time PCR. The expression rate of Nanog gene in experimental cell clones obtained by the short-term cultivation of spermatogonia cells in the presence of Sertoli cells was 200 times higher than in freshly isolated spermatogonia cells. The product of Plzf gene expression was found both in freshly isolated spermatogenic cells and in cell clones obtained in vitro. After long-term cultivation of spermatogonia on Sertoli cells, we observed in vitro differentiation to the lineage of spermatogenesis and formation of separate motile sperm cells after 30–33 days. At this stage, the cell population was heterogeneous. In the absence of Sertoli cells, the differentiation of boar spermatogonia cells in culture stopped after 7 days of cultivation. The data show that the cultivation of boar spermatogonia cells on Sertoli cells contributes to their in vitro differentiation to the lineage of spermatogenesis and can help to obtain boar sperm cell culture.