An evaluation of malaria transmission and epidemiology in the Amazonian city of Belém over the last 70 years shows that (1) Anopheles darlingi, reported to be eradicated in 1968, reappeared in the mid 1990s, with a marked increase in abundance between 1997 to 1999 in two of three districts sampled; (2) An. darlingi and An. aquasalis are each implicated in current malaria transmission in different districts of the city; (3) mosquito species diversity (in Anopheles subgenus Nyssorhynchus) has increased from two in the 1930s to six in the 1940s to 10 in the 1990s; (4) there is no overall correlation between malaria case incidence and human population size from 1940 to 1996 in Belém; (5) however, the total number of malaria cases has increased significantly since the late 1970s and over the short term from 1993 to 1999; and (6) interestingly, the short term increases are due solely to cases of Plasmodium vivax infection; cases of P. falciparum malaria are declining (significantly for Pará state only). The reappearance of An. darlingi may be a result of the continued expansion of Belém into the surrounding forest in the 1990s. In the absence of preventative measures, we predict an increase in local outbreaks of malaria in the DAENT and DAICO districts where the population sizes of An. darlingi are increasing.

Several animal experimental models have been used in the study of malignant gliomas. The objective of the study was to test the efficacy of a simple, reproducible and low cost animal model, using human cells of glioblastoma multiforme (GBM) xenotransplantated in subcutaneous tissue of Wistar rats, immunosuppressed with cyclosporin given by orogastric administration, controlled by nonimunosuppressed rats. The animals were sacrificed at weekly intervals and we have observed gradual growth of tumor in the immunosuppressed group. The average tumor volume throughout the experiment was 4.38 cm 3 in the immunosuppressed group, and 0.27 cm 3 in the control one (p<0.001). Tumors showed histopathological hallmarks of GBM and retained its glial identity verified by GFAP and vimentin immunoreaction. Immunosuppression of rats with cyclosporin was efficient in allowing the development of human glioblastoma cells in subcutaneous tissues. The model has demonstrated the maintenance of most of the histopathological characteristics of human glioblastoma in an heterotopic site and might by considered in research of molecular and proliferative pathways of malignant gliomas. Key words: animal model, Wistar rats, cyclosporin, glioblastoma, xenotransplant.Modelo murino de xenotransplante de glioblastoma humano com imunossupressão utilizando ciclosporina orogástrica RESUMO Vários modelos animais têm sido avaliados no estudo dos gliomas e até o momento nenhum pôde ser considerado ideal. O objetivo deste trabalho é verificar a eficácia de um modelo animal simples, reprodutível e de baixo custo. Utilizamos células humanas de glioblastoma multiforme (GBM) xenotransplantadas em ratos Wistar, submetidos a imunossupressão com ciclosporina administrada por via orogástrica. Células tumorais foram implantadas no tecido subcutâneo dos ratos imunossuprimidos com ciclosporina, sendo o controle feito em ratos não imunossuprimidos. Os animais foram sacrificados em intervalos semanais e foi observado crescimento progressivo do tumor no grupo imunossuprimido. A média do volume tumoral em todo o experimento foi de 4,38 cm 3 no grupo imunossuprimido e 0,27 cm 3 no grupo controle (p<0,001). Os tumores apresentavam características histopatológica do GBM e mantinham sua identidade glial, verificadas por imunoreação para GFAP e vimentina. A imunossupressão dos ratos com ciclosporina

In this work we present and discuss some results concerning the application of colloidal semiconductor quantum dots for cancer diagnostic. We have prepared and applied different core-shell semiconductor quantum dots such as Cadmium Teluride-Cadmium Sulfide (CdTe-CdS) and Cadmium SulfideCadmium Hydroxide (CdS/Cd(OH) 2 ). For the purpose of diagnostic with living cells, the CdS/Cd(OH) 2 presented best results, maintaining high levels of luminescence as well high stability in biological media. The quantum dots were obtained in aqueous medium, by reacting Cd 2+ and S 2-in the presence of sodium polyphosphate as the stabilizing agent. Subsequent surface passivation with Cd(OH) 2 was carried out to improve luminescence. At a pH of 7,2 the quantum dots were functionalized with a 0.01% glutaraldehyde solution and then, incubated with living healthy and neoplastic cells (glial, glioblastoms and cervical) and tissues (breast) in culture medium. Tissue and cell staining were evaluated by the laser scanning confocal microscopy. Fluorescence Microscopy was used as a primary tool in order to explore the labeling of the samples. The procedure presented in this work, shown to be very efficient as a potential tool for fast and precise cancer diagnostic.

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In this work we present the preparation, characterization and conjugation of colloidal core shell CdS-Cd(OH) 2 quantum dots to health and cancer glial rats living cells in culture media. The particles were obtained via colloidal synthesis in aqueous medium, with final pH=7.3-7.4. Laser Scan Confocal Microscopy (LSCM) and Fluorescence Microscopy were used to evaluate fluorescence intensities and patterns of health and cancer (glioblastoma) glial cells labeled with the quantum dots in different time intervals. Health and cancer glial cells clearly differ in their fluorescence intensities and patterns. These different fluorescence intensities and patterns may be associated to differences concerning cellular membrane and metabolic features of health and cancer cells. The results obtained indicate the potential of the methodology for fast and precise cancer diagnostics.