[The association between aeroallergenic structures and allergic rhinitis: a study on northern Vietnam]. / Assotsiatsiya mezhdu strukturami aeroallergenov i allergicheskim rinitom: issledovanie o severe V'etnama.

Recently, there has been an increase in the number of patients with allergic rhinitis (AR) and the number of publications devoted to this problem is increasing. The main etiological factors of AR are pollen of trees, meadow and weeds, as well as mold spores, household allergens and epidermis of animals. Epidemiological studies have found that the prevalence and structure of AR are influenced by regional characteristics, such as the climatic and geographical and social characteristics of the region, and successively therapeutic and preventive algorithms in AR are also different. AIM: To examine the phenotype of the incidence of AR in connection with the characteristics of aeroallergens under the influence of climatic and geographical conditions in northern Vietnam, to make a new contribution to knowledge about AR in Asia and to increase the effect of treatment and prevention in this territory. MATERIALS AND RESEARCH METHODS: The study was conducted in the period from 06.2018 to 09.2018 on the basis of the ENT department of Thainguyen Central Hospital, Vietnam. A total of 556 patients with pathology of ENT organs aged 18 to 70 years were examined, 158 cases of chronic rhinitis were revealed. Among data from 158 patients, 64 patients were diagnosed with AR. We used otorhinolaryngological examination, a standard specific allergological examination and carried out aeropolyneological research in the city of the northern Vietnam, from 06.2018 to 06.2019. RESULT: The aerobiological spectrum is dominated by pollen from the families Moraceae, Urticaceae, Poaceae, Acacia, Artemisia, fern spores and fungal spores from the genus Alternaria. Among patients with chronic rhinitis, 40% were diagnosed with AR, 98.44% of them year-round or perennial AR, with predominant sensitization to house dust mites and molds, much more often to plant pollen. Among 9 (14.06%) patients diagnosed with a polyp of the nasal cavity, 6 (9.37%) patients had increased levels of specific IgE in the blood to a mixture of molds. Sensitization in patients with AR with hypertrophy of the mucous membrane of the nasal cavity is predominant on house dust. CONCLUSION: Predominantly, AR in northern Vietnam was year-round. Especially the connection between the formation of a polyp of the nasal cavity and hypersensitivity to fungal spores has been indicated, which may also indicate the role of social factors in further recommendations for the diagnosis, treatment and prevention of AR in patients living in North Vietnam.

A numerical model of birch pollen emission and dispersion in the atmosphere. Description of the emission module.

A birch pollen emission model is described and its main features are discussed. The development of the model is based on a double-threshold temperature sum model that describes the propagation of the flowering season and naturally links to the thermal time models to predict the onset and duration of flowering. For the flowering season, the emission model considers ambient humidity and precipitation rate, both of which suppress the pollen release, as well as wind speed and turbulence intensity, which promote it. These dependencies are qualitatively evaluated using the aerobiological observations. Reflecting the probabilistic character of the flowering of an individual tree in a population, the model introduces relaxation functions at the start and end of the season. The physical basis of the suggested birch pollen emission model is compared with another comprehensive emission module reported in literature. The emission model has been implemented in the SILAM dispersion modelling system, the results of which are evaluated in a companion paper.

Antiarrhythmic activity of phytoadaptogens in short-term ischemia-reperfusion of the heart and postinfarction cardiosclerosis.

A course of treatment (16 mg/kg orally during 5 days) by Aralia mandshurica or Rhodiola rosea extracts reduced the incidence of ischemic and reperfusion ventricular arrhythmias during 10-min ischemia and 10-min reperfusion. Extracts of Eleutherococcus senticosus, Leuzea carthamoides, and Panax ginseng did not change the incidence of ischemic and reperfusion arrhythmias. Chronic treatment by aralia, rhodiola, and eleutherococcus elevated the ventricular fibrillation threshold in rats with postinfarction cardiosclerosis. Ginseng and leuzea did not change this parameter in rats with postinfarction cardiosclerosis.

Detection of aneuploidy in human oocytes and corresponding first polar bodies by fluorescent in situ hybridization.

PURPOSE: The purpose of the study was to investigate the reliability of the fluorescent in situ hybridization (FISH) analysis of the first polar body (IPB) for cytogenetic evaluation of human oocytes as a method of choice in preimplantation diagnosis of chromosomal aneuploidies. DESIGN: Human unfertilized oocytes and their extruded IPB were analyzed using the directly labeled fluorescence alpha-satellite DNA probes to chromosomes X and 18. RESULTS: Paired signals for chromosomes X and 18 were observed in the second meiotic prophase (MII) of unfertilized oocytes and their extruded IPB. In the series of 156 unfertilized oocytes in which the number of X chromosome- and chromosome 18-specific signals were analyzed in both MII and IPB, five nondisjunction events have been detected, with corresponding signals in MII and their IPB: missing signals in MII corresponded to extra signals in their IPB and extra signals in MII corresponded to missing signals in IPB. In one oocyte chromosome 18 nondisjunction was detected, with both chromosome 18 signals in MII and no chromosome 18 signal in IPB. In four oocytes chromatid malsegregations for chromosome X or chromosome 18 were detected: in two oocytes, three of four chromosome 18 signals were present in MII, with only one in IPB, and in the other two oocytes, three of four chromosome signals were present in MII, with only one left in IPB. CONCLUSIONS: The data suggest the possibility of detecting chromosomal aneuploidy in oocytes through cytogenetic analysis of their corresponding IPB by FISH as a possible approach for preimplantation diagnosis of major chromosomal trisomies.

[The quantitative study of the areas of active rDNA location and of the other parameters of the interphase nucleolus detectable by silver staining during the cell differentiation of the rat trophoblast]. / Kolichestvennoe issledovanie zon lokalizatsii aktivnosti rDNK i drugikh parametrov interfaznogo iadryshka, vyiavliaemykh metodom serebreniia v khode differentsirovki kletok trofoblasta krysy.

Different quantitative parameters of nucleolar silver staining have been studied in the cambial rat trophoblast cells on the 12th, 13th and 14th days of gestation. It has been shown that the number of Ag-positive granules in the nucleoli varied from 10 to 120. The number and the total area of silver stained granules in the nuclei increased progressively in the course of polyploidization, but was not doubled passing to the next ploidy level. Nevertheless, nucleolar area increased proportionally to the ploidy degree. The mean number and the total area of Ag-stained granules as well as the nucleolar area estimated for each ploidy level did not change significantly in the course of placenta development, suggesting an unchanged level of NOR activity at the studied stages of trophoblast cell differentiation. The data obtained on the interphase nucleoli differ from the data of the analysis of the metaphase Ag-NOR at the same period of placenta development, suggesting a diversity in the interphase and metaphase NOR organization. A proportion of cells with different number of nucleoli in the cambial rat trophoblast cells was maintained unchanged in the studied period of the placenta development, the majority (80-90%) of cells contained from 1 to 3 nucleoli. Such a proportion was similar in the cells of different levels of ploidy up to 16c. In this connection the association of NORs is suggested to be in relation with switching from the polyploid mitotic cycle to the endoreduplication leading to polyteny.

[Cytological research on the argentophilic nucleolus-organizer regions of the metaphase chromosomes in parthenogenetic mouse embryos]. / Tsitologicheskoe issledovanie argentofil'nykh iadryshkoobrazuiushchikh raionov metafaznykh khromosom u partenogeneticheskikh zarodyshei myshei.

Silver staining technique visualizing argentophilic nucleolus organizer regions (Ag-NORs) was used for studying parthenogenetic mouse embryos produced by artificial activation of oocytes in Ca(2+)-Mg(2+)-free medium. Ag-NOR-containing chromosomes were detected in metaphases of parthenogenetic embryos during six successive cleavage divisions starting with the two-cell stage. The frequency of metaphases with varying AG-NOR number in diploid parthenogenones was similar to that in the control (fertilized) embryos. Average number of metaphase Ag-NOR chromosomes (calculated per diploid chromosome set) in haploid parthenogenones exceeded that in the control; in some cases all NORs were stained by silver. This is evidence that latent ribosomal cistrons in some chromosomes can be activated.

[The nucleolus organizer regions of the metaphase chromosomes in cambial cell populations of mouse and rat placenta]. / Iadryshkoobrazuiushchie raiony metafaznykh khromosom v kambial'nykh kletochnykh populiatsiiakh platsenty myshi i krysy.

The number of silver-stained nucleolus organizing regions (Ag-NORs) was counted in metaphase plates of the fetal part of placenta of mice and rats and in the tissues of their embryos. On day 9 of mouse gestation and on day 12 of rat gestation, up to 82% of metaphases in the fetal part of placenta have the highest possible number of chromosomes with Ag-NORs (9-10 for mice and 5-6 for rats). In the later embryogenesis (day 10 for mice and day 14 for rats), a great number of metaphases have either no Ag-NORs (34.9% for mice, 17.9% for rats), or only 1-2 Ag-NOR-chromosomes (17.4% for mice and 14.5% for rats). But in the tissues of embryos being on the same embryonic stages the changes in frequency of metaphases with different numbers of Ag-NOR-chromosomes have proved to be less obvious. In the differentiated polyploid placenta cells the number of chromosomes with Ag-NORs can be considerably lower than in diploid ones. It is proposed that the changes in frequency of metaphases with different numbers of Ag-NOR-chromosomes may reflect the regulation of ribosomal gene transcription in the embryogenesis, in particular, in differentiation of cambial cell populations of rodent placenta.

The silver-stained NOR and argentophilic nuclear proteins in early mouse embryogenesis: a cytological study.

Silver staining (Howell and Black, 1980) was used in light and electron microscopic studies for detecting the localization of argentophilic nuclear proteins in fertilized ova and cleaving mouse embryos. No silver-stained nucleolus organizing regions (NORs) (Ag-NORs) were visualized in the metaphase chromosomes of the first cleavage mitosis. From the 2-cell stage on, metaphase chromosomes contained Ag-NORs. Argentophilic proteins were detected in the pronuclei of the 1-cell embryos, i.e. before transcription of the ribosomal genes started. After fertilization these proteins accumulated on the decondensing sperm chromatin and telophase maternal chromosomes, then migrated into the pronuclei to be stored in pronucleoli, and, during mitosis, were transferred into the cytoplasm. In the metaphase chromosomes of the cleaving embryos Ag-NORs adequately reflected the transcriptional activity of the ribosomal genes, whereas in pronuclei of the 1-cell stage embryos argentophilic proteins were not involved in this process, but are likely to play a part in the formation and maturation of pronucleoli, and in the cell cycle regulation.

[The first cycle of DNA replication in parthenogenetic mouse embryos]. / Izuchenie pervogo tsikla replikatsii DNK u partenogeneticheskikh zarodyshei myshei.

Dynamics of the first cell cycle in parthenogenetic mouse embryos derived from ethanol-activated eggs was studied using 3H-thymidine. DNA synthesis starts within 5 h and is terminated within 10 h after activation: it lasts ca. 6 h. Changes in the intensity of 3H-thymidine incorporation and in the distribution of radioactive label between haploid and diploid parthenogens were observed. 3H-thymidine was shown to incorporate into pronucleoli of diploid parthenogens and late-labeled heterochromatin blocks were bound in both diploid and haploid pronuclei. The structure of the first cell cycle in parthenogenetic and normal embryos is discussed.

[The ultrastructure and argentophilic properties of the nucleolus organizer and centromeric regions of the chromosomes in early mouse embryogenesis]. / Ul'trastruktura i argentofil'nye svoistva iadryshkoobrazuiushchikh i tsentromernykh raionov khromosom v rannem émbriogeneze myshi.

The Ag-staining of metaphase chromosomes in one-cell mouse embryos shows that the nucleolus organizer regions (NORs) are Ag-negative, whereas centromeric regions (CRs) are Ag-positive. Starting from 8-16-cell embryos, NORs stained by AgNO3 constantly, CRs remaining argentophobic. On the ultrathin sections of multicell embryos, Ag(+)-NORs differ from the chromosomal arms: they consist of loosely filaments about 6-8 nm in diameter, characterized by a low electron density. On the contrary, at one-cell stage Ag(-)-NORs are not morphologically identified: chromosomal bodies consist of uniform DNP-fibrils about 20 nm in diameter. These data permit to suppose that extended rDNA may form supranucleosomal and nucleosomal DNP-fibrils in the absence of Ag-proteins. The Ag(+)- and Ag(-)-CRs contain 10-20 nm DNP-fibrils mainly, although their density at multicell stages is higher than in one-cell mouse embryos.

[Cytological research on localizing argentophilic proteins in one-cell mouse embryos]. / Tsilogicheskoe issledovanie lokalizatsii argentofil'nykh belkov u odnokletochnykh zarodyshei myshei.

Localization of argentophilic proteins on mouse one-cell embryos has been studied under light and electron microscope using the silver staining that reveals transcriptionally active nucleolus-organizing chromosome regions (NORs). Although argentophilic proteins are observed in NORs of metaphase chromosomes only after the second cleavage division, they can be detected in nuclear apparatus of one-cell embryos, that is at the stage when ribosomal genes are not yet transcribed. Argentophilic proteins are visualized on the surface of decondensing chromatin of the spermatozoon head and on maternal telophase chromosomes immediately after the fertilization. They migrate into pronuclei and are accumulated in pronucleoli. During mitosis argentophilic proteins bind to chromosomes and move to cytoplasm. The importance of argentophilic proteins at the initial stages of mammalian embryogenesis is discussed.