Ergodicity and digital texts

Na passagem do texto físico para o texto digital ocorre uma quebra da linearidade da página impressa, que afecta a forma como a recepção se alia à produção através da performatividade característica das novas narrativas. A ruptura do limite material do texto, permitida pela hipertextualidade, obriga a uma construção de sentidos diferente, que assenta na exploração de um texto maior. A introdução do hipermedia vem depois ampliar e complexificar a ideia de hipertextualidade, ao fazer convergir linguagens diversas, num processo interactivo que se assemelha ao processo da própria criação. A partir de estímulos e aberturas do trabalho digital, os textos ergódicos constroem a imaterialidade da significação em espaços singularizados de materialidade algorítmica. Perante um texto destituído de corpo próprio ou único, pretende-se discutir a forma como a textualidade electrónica assiste a esta desmaterialização e a conduz, e como o discurso hipermedia se desloca entre linguagens e suportes multimédia diferentes.ABSTRACT: Whilst breaking the linearity of the printed page, the passage from the physical text to a digital one has blurred the limits between reception and production and has shaped different narrative performances. Hypertextuality has shattered the limits of the text and has simultaneously required the construction of meaning by exploring a major text. Eventually, hypermedia has amplified and complexified that hypertextuality by being able to converge diverse languages, in an interactive process that resembles the actual creation activity. In response to the nodes and stimuli of the digital work, ergodic texts coexist within a customized space of algorithmic materiality and signification immateriality. In this paper we want to discuss how the bodiless but crowded electronic textuality leads this dematerialization as the hypermedia discourse flickers among different languages and multimedia devices.info:eu-repo/semantics/publishedVersio

Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressions

The malaria treatment recommended by the World Health Organization involves medicines derived from artemisinin, an active compound extracted from the plant Artemisia annua, and some of its derivatives, such as artesunate. Considering the lack of data regarding the genotoxic effects of these compounds in human cells, the objective of this study was to evaluate the cytotoxicity and genotoxicity, and expressions of the CASP3 and SOD1 genes in a cultured human hepatocellular liver carcinoma cell line (HepG2 cells) treated with artemisinin and artesunate. We tested concentrations of 2.5, 5, 7.5, 10, and 20 μg/mL of both substances with a resazurin cytotoxicity assay, and the concentrations used in the genotoxicity experiments (2.5, 5, and 10 μg/mL) and gene expression analysis (5 mg/mL) were determined. The results of the comet assay in cells treated with artemisinin and artesunate showed a significant dosedependent increase (P < 0.001) in the number of cells with DNA damage at all concentrations tested. However, the gene expression analysis revealed no significant change in expression of CASP3 or SOD1. Our data showed that although artemisinin and artesunate exhibited genotoxic effects in cultured HepG2 cells, they did not significantly alter expression of the CASP3 and SOD1 genes at the doses tested. ©FUNPEC-RP

Genistein at Maximal Physiologic Serum Levels Induces G0/G1 Arrest in MCF-7 and HB4a Cells, But Not Apoptosis

Several studies have demonstrated that a balanced diet can contribute to better human health. For this reason, soy-based food and pure isoflavones (pills) are one of the most consumed. The association of this consumption and lower risks of chronic diseases and cancer is well established for the Asian population and has been attracting thw attention of people worldwide, especially women at menopause who seek to alleviate the symptoms associated with the lack of estrogen. Despite positive epidemiological data, concerns still exist because of conflicting results found in scientific literature with relation to the role of isoflavones in breast and hormone-related cancers. The aim of our study was to investigate the cytotoxicity, induction of apoptosis, and changes in apoptosis-related genes of maximal physiological serum levels of the isoflavone genistein (Gen) in MCF-7 tumoral cells and in HB4a non-tumoral cells. In addition, induction of cell cycle arrest was also investigated. Only supraphysiological levels of Gen (50 and 100M) were cytotoxic to these cell lines. Concentrations of 10 and 25M did not induce apoptosis and significant changes in expression of the studied genes. Positive results were found only in cell cycle analysis: G0/G1 delay of MCF-7 cells in both concentrations of Gen and at 25M in HB4a cells. It is the first study investigating effects of Gen in the HB4a cell line. Thus, despite the lack of apoptosis induction (generally found with high concentrations), Gen at physiologically relevant serum levels still exerts chemopreventive effects through the modulation of cell cycle.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES