8 research outputs found

    Comparison of in vivo and in vitro preimplantation embryo development in OXYS and WAG rats

    Get PDF
    OXYS rats are the model of precocious senescence. Numerous studies addressed physiology and behavior in rats of this strain during a postnatal period of their life, however, preimplantation development in OXYS rats has not yet been investigated. This study is addressing preimplantation embryonic development in OXYS rats both in vivo and in vitro. Rats of the WAG strain were used as controls. For studying the in vivo development, the embryos were collected from OXYS and WAG rats on day 5 post coitum, the stages of embryo development were estimated, the percentage of embryos at blastocyst stage and the cell numbers in these blastocysts were counted. In a special experiment, for studying in vitro development, the embryos were collected from both rat strains on day 4 post coitum and were cultured in vitro in P1 medium for 48 hours with or without supplementation with IGF-1 (200 ng/mL). Thereafter the percentage of embryos at blastocyst stage and the cell numbers in these blastocysts were counted in the same manner as for the in vivo experiment. This study reports that in vivo derived blastocysts of OXYS rats contain fewer cells on day 5 of their development than in vivo derived blastocysts of WAG rats. In vitro culture of the early preimplantation embryos in P1 medium mitigated the difference in the rate of embryo development between these two strains, the addition of IGF-1 into culture medium exerts neither negative nor positive effect on the rate of in vitro embryo development in rats of both strains

    Studies of Biofilm Formation in Non-Pigmented and Plasmid-Deprived Mutants of <I>Yersinia pestis</I> on Biotic Surfaces, <I>in vivo</I> and <I>in vitro</I> Conditions

    Get PDF
    In non-pigmented and plasmid-deprived mutants – isogenic variants of highly virulent Yersinia pestis 231 strain – studied is the mechanism of biofilm formation on biotic surfaces, both in vitro (on the laboratory model of nematode Caenorhabdiitis elegans) and in vivo (inside the alimentary tract of Nosopsyllus laeviceps flea). It is determined that spontaneous loss of ability to form biofilms and generate pigmented colonies in the mutants is probably caused not only by the deletion of the whole chromosome pigmentation fragment, but also by a point(single base) mutation in structural hms operon. It is demonstrated that the absence of pCad, pFra or pPst plasmids does not have an impact on the ability of plasmid-deprived mutants to form biofilm on the cuticle of nematode C. elegans

    Studies of West Nile Virus Circulation in the Territory of the Saratov Region in 2010

    Get PDF
    Presented are the results of ecological and epizootiological surveillance of the territory of the Saratov region, which was carried out in autumn of 2010. The surveillance was aimed at detection of West Nile (WN) virus circulation and premises for WN Fever natural focus formation. It is demonstrated that in 2010 WN virus circulation took place in damp biotopes of the Saratov region territory, and that common species of small mammals were involved in it. Presented are the results of analysis of the WN virus role in the infectious pathology in the territory of the Saratov region

    Conditions for Virus Circulation and Premises for Natural West Nile Fever Foci Formation in the Territory of the Saratov Region

    Get PDF
    Local climate change (rise of mean temperatures and amount of precipitation, prolongation of frost-free season) triggers further distribution, and increase in numbers of animals – carriers and vectors of West Nile fever virus in the territory of the Saratov region. Based on the results of ecological-epizootiological monitoring (2006–2012) traced out have been the species composition, abundance dynamics, and character of distribution of birds habitant in aquatic and anthropogenic complexes, mosquitoes and Ixodidae ticks. Investigated are possible causes of West Nile fever nosoarea expansion, related to ecology of migrating birds wintering in Africa. Persistent circulation of the virus in intra-zonal inundated biocoenosis facilitates formation of secondary natural foci of West Nile fever and factors into epidemic complications as regards this particularly dangerous vector-borne infection. On the basis of analytical data concerning hydrographic network density, fauna structure, population numbers of birds and mosquitoes – potential carriers and vectors of WNF, epizootiological and epidemiological surveillance, designed has been expectation-driven forecasting map chart which illustrates possibility of sustainable WNF foci formation in various territories of the Saratov region

    Distribution and Abundance of Ticks and Fleas, Infectious Diseases Vectors, in the Semi-Desert Zone of Saratov Trans-Volga Region

    No full text
    Many-years observations demonstrate that six species of the ticks inhabit semi-desert zone of Saratov Trans-Volga Region. Nine flea species are registered at small mammalians in the near-water biotopes. The dominating ectoparasite species can be of significance at present as dangerous infectious diseases vectors. They are 2 ticks species and 3 flea species. Epizootiologic monitoring to be carried out is associated with control of abundance of ectoparasite species conventional for this territory, and with detection of new species possessing condition to inhabit it

    The New Data on Distribution of Ixodic Ticks and Agents of Natural-Focal Infections Transferred by Them in Saratov Region

    No full text
    The expansion of areas and increase of the number of Ixodes ticks lead to distribution of ixodic tick-borne borreliosis agent in the territory of Saratov region. There exists the potential danger of activation of the natural foci of tularemia, formation of tick-borne encephalitis and Crimean hemorrhagic fever foci, their reservoirs and vectors being the ixodic ticks inhabiting the territory of the region

    Therapeutic effects of hipsc-derived glial and neuronal progenitor cells-conditioned medium in experimental ischemic stroke in rats

    No full text
    Transplantation of various types of stem cells as a possible therapy for stroke has been tested for years, and the results are promising. Recent investigations have shown that the administration of the conditioned media obtained after stem cell cultivation can also be effective in the therapy of the central nervous system pathology (hypothesis of their paracrine action). The aim of this study was to evaluate the therapeutic effects of the conditioned medium of hiPSC-derived glial and neuronal progenitor cells in the rat middle cerebral artery occlusion model of the ischemic stroke. Secretory activity of the cultured neuronal and glial progenitor cells was evaluated by proteomic and immunosorbent-based approaches. Therapeutic effects were assessed by overall survival, neurologic deficit and infarct volume dynamics, as well as by the end-point values of the apoptosis-and inflammation-related gene expression levels, the extent of microglia/macrophage infiltration and the numbers of formed blood vessels in the affected area of the brain. As a result, 31% of the protein species discovered in glial progenitor cells-conditioned medium and 45% in neuronal progenitor cells-conditioned medium were cell type specific. The glial progenitor cell-conditioned media showed a higher content of neurotrophins (BDNF, GDNF, CNTF and NGF). We showed that intra-arterial administration of glial progenitor cells-conditioned medium promoted a faster decrease in neurological deficit compared to the control group, reduced microglia/macrophage infiltration, reduced expression of pro-apoptotic gene Bax and pro-inflammatory cytokine gene Tnf, increased expression of anti-inflammatory cytokine genes (Il4, Il10, Il13) and promoted the formation of blood vessels within the damaged area. None of these effects were exerted by the neuronal progenitor cell-conditioned media. The results indicate pronounced cytoprotective, anti-inflammatory and angiogenic properties of soluble factors secreted by glial progenitor cells. © 2021 by the authors. Licensee MDPI, Basel, Switzerland
    corecore