61 research outputs found

    Effect of Cultural Priming on Social Behavior and EEG Correlates of Self-Processing

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    Humans are social beings and the self is inevitably conceptualized in terms of social environment. The degree to which the self is perceived as fundamentally similar or fundamentally different from other people is modulated by cultural stereotypes, such as collectivism and individualism. These stereotypes are not hardwired in our brains and individuals differ in the degree to which they adopt the attitudes that define their culture. Moreover, individuals can acquire multiple sets of cultural knowledge and, depending on the context, either individualistic or collectivistic cultural mindset could be activated. In this study, we used cultural priming techniques to activate either individualistic or collectivistic mindset and investigated the association between source-level EEG connectivity in the default mode network (DMN) and spontaneous self-related thoughts in the subsequent resting state. Afterward, participants performed a social interaction task, in which they were allowed to choose between friendly, avoidant, or aggressive behavior. After collectivism priming, self-related thoughts were associated with increased connectivity of DMN with the right temporoparietal junction (TPJ), which is involved in taking the perspective of others and is more active in representatives of collectivistic cultures, whereas after individualism priming they were associated with increased connectivity with the temporal pole, which is involved in self/other discrimination and is more active in representatives of individualistic cultures. Individual differences in the intensity of post-priming self-related thoughts and the strength of DMN-temporal pole connectivity predicted individual differences in behavior during the social interaction task, with individualistic mindset predisposing to more friendly and trustful social behavior

    Identification of Spiro-Fused Pyrrolo[3,4-a]pyrrolizines and Tryptanthrines as Potential Antitumor Agents: Synthesis and In Vitro Evaluation

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    A series of heterocyclic compounds containing a spiro-fused pyrrolo[3,4-a]pyrrolizine and tryptanthrin framework have been synthesized and studied as potential antitumor agents. Cytotoxicity of products was screened against human erythroleukemia (K562) and human cervical carcinoma (HeLa) cell lines. Among the screened compounds. 4a, 4b and 5a were active against human erythroleukemia (K562) cell line, while 4a and 5a were active against cervical carcinoma (HeLa) cell line. In agreement with the DNA cytometry studies, the tested compounds have achieved significant cell-cycle perturbation with higher accumulation of cells in G2/M phase and induced apoptosis. Using confocal microscopy, we found that with 4a and 5a treatment of HeLa cells, actin filaments disappeared, and granular actin was distributed diffusely in the cytoplasm in 76–91% of cells. We discovered that HeLa cells after treatment with compounds 4a and 5a significantly reduced the number of cells with filopodium-like membrane protrusions (from 63 % in control cells to 29% after treatment) and a decrease in cell motility

    Exchange reactions control for selective separation of glyoxylic acid in technological mixtures of glyoxal oxidation

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    Separation of glyoxylic acid from unpurified multicomponent technological mixtures, resulting in the process of direct oxidation of glyoxal, and preparation of sodium glyoxylate are developed. The mixtures are treated with an optimal amount of CaCO3, which has to be prespecified by acidic–basic titration of the technological mixtures. Both separation of glyoxylic acid and preparation of sodium glyoxylate take place owing to ionic exchange reactions: calcium glyoxylate is easily converted into glyoxylic acid by action of oxalic acid. Reaction with Na2CO3 leads to the formation of sodium glyoxylate

    Exchange reactions control for selective separation of glyoxylic acid in technological mixtures of glyoxal oxidation

    No full text
    Separation of glyoxylic acid from unpurified multicomponent technological mixtures, resulting in the process of direct oxidation of glyoxal, and preparation of sodium glyoxylate are developed. The mixtures are treated with an optimal amount of CaCO3, which has to be prespecified by acidic–basic titration of the technological mixtures. Both separation of glyoxylic acid and preparation of sodium glyoxylate take place owing to ionic exchange reactions: calcium glyoxylate is easily converted into glyoxylic acid by action of oxalic acid. Reaction with Na2CO3 leads to the formation of sodium glyoxylate
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