2,266 research outputs found
Sobre a identidade profissional na Enfermagem: reconsiderações pontuais em visão filosófica
The molecular detection of different Leishmania species within sand flies from a cutaneous and visceral leishmaniasis sympatric area in Southeastern Brazil
Chagas disease in the State of Pernambuco, Brazil: analysis of admissions and mortality time series
Secular Evolution and the Formation of Pseudobulges in Disk Galaxies
We review internal processes of secular evolution in galaxy disks,
concentrating on the buildup of dense central features that look like
classical, merger-built bulges but that were made slowly out of disk gas. We
call these pseudobulges. As an existence proof, we review how bars rearrange
disk gas into outer rings, inner rings, and gas dumped into the center. In
simulations, this gas reaches high densities that plausibly feed star
formation. In the observations, many SB and oval galaxies show central
concentrations of gas and star formation. Star formation rates imply plausible
pseudobulge growth times of a few billion years. If secular processes built
dense central components that masquerade as bulges, can we distinguish them
from merger-built bulges? Observations show that pseudobulges retain a memory
of their disky origin. They have one or more characteristics of disks: (1)
flatter shapes than those of classical bulges, (2) large ratios of ordered to
random velocities indicative of disk dynamics, (3) small velocity dispersions,
(4) spiral structure or nuclear bars in the bulge part of the light profile,
(5) nearly exponential brightness profiles, and (6) starbursts. These
structures occur preferentially in barred and oval galaxies in which secular
evolution should be rapid. So the cleanest examples of pseudobulges are
recognizable. Thus a large variety of observational and theoretical results
contribute to a new picture of galaxy evolution that complements hierarchical
clustering and merging.Comment: 92 pages, 21 figures in 30 Postscript files; to appear in Annual
Review of Astronomy and Astrophysics, Vol. 42, 2004, in press; for a version
with full resolution figures, see
http://chandra.as.utexas.edu/~kormendy/ar3ss.htm
Thrombocytopenia in the experimental leptospirosis of guinea pig is not related to disseminated intravascular coagulation
BACKGROUND: Thrombocytopenia is commonly observed in severe leptospirosis. However, previous studies on coagulation alterations during leptospirosis resulted in inconsistent conclusions. Some findings showed that the prominent levels of thrombocytopenia observed in severe leptospirosis did not reflect the occurrence of disseminated intravascular coagulation (DIC) syndrome, while the others reached the conclusion that the hemorrhages observed in leptospirosis were due to DIC. The aim of this study is to elucidate whether DIC is an important feature of leptospirosis. METHODS: The leptospirosis model of guinea pig was established by intraperitoneal inoculation of Leptospira interrogans strain Lai. Hematoxylin and eosin (HE) staining, electron microscopy and immunohistochemistry staining were used to detect the pathologic changes. Platelet thrombus or fibrin thrombus was detected by HE, Martius Scarlet Blue (MSB) staining and electron microscopy. Hemostatic molecular markers such as 11-dehydrogenate thromboxane B2 (11-DH-TXB2), thrombomodulin (TM), thrombin-antithrombin III complex (TAT), D-Dimer and fibrin (ogen) degradation products (FDPs) in the plasma were examined by quantitative enzyme-linked immunosorbent assay (ELISA) to evaluate the hematological coagulative alterations in leptospirosis models. RESULTS: Pulmonary hemorrhage appeared in the model guinea pig 24 hours after leptospires intraperitoneal inoculation, progressing to a peak at 96 hours after the infection. Leptospires were detected 24 hours post-inoculation in the liver, 48 hours in the lung and 72 hours in the kidney by immunohistochemistry staining. Spiral form of the bacteria was initially observed in the liver, lung and kidney suggestive of intact leptospires, granular form of leptospires was seen as the severity increased. Platelet aggregation in hepatic sinusoid as well as phagocytosis of erythrocytes and platelets by Kupffer cells were both observed. Neither platelet thrombus nor fibrin thrombus was found in the liver, lung or kidney via morphological observation. Thrombocytopenia was observed in all infected guinea pigs of our experimental leptospirosis study. Analysis of hematologic molecular markers showed that 11-DH-TXB2 and TM in the plasma were elevated significantly. TAT that reflects the thrombin activation had a trend of decline after infection. Although D-dimer and FDPs increased statistically, the increasing may not bear clinical significance. CONCLUSION: Pathologic and hematological studies for experimental leptospirosis of guinea pig indicated that the thrombocytopenia found in guinea pigs did not correlate with the occurrence of DIC. The platelet aggregation and Kupffer cells phagocytosis might be the potential causes of thrombocytopenia in severe leptospirosis
Seroprevalence and factors associated with herpes simplex virus type 2 among HIV-negative high-risk men who have sex with men from Rio de Janeiro, Brazil: a cross-sectional study
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Previous issue date: 2009Fundação Oswaldo Cruz. Instituto de Pesquisa Clínica Evandro Chagas. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Instituto de Pesquisa Clínica Evandro Chagas. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Instituto de Comunicação e Informação Científica e Tecnológica em Saúde. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Instituto de Pesquisa Clínica Evandro Chagas. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Instituto de Pesquisa Clínica Evandro Chagas. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Instituto de Pesquisa Clínica Evandro Chagas. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Instituto de Pesquisa Clínica Evandro Chagas. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Instituto de Pesquisa Clínica Evandro Chagas. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Instituto de Pesquisa Clínica Evandro Chagas. Rio de Janeiro, RJ, Brasil.Background: Herpes simplex virus type 2 (HSV-2) is the leading cause of genital ulcer disease in
developing countries, including Brazil, and is especially prevalent among men who have sex with
men (MSM). HSV-2 infection represents a risk factor for the acquisition and transmission of other
sexually transmitted diseases. The goal of the present cross-sectional study was to estimate HSV-
2 seroprevalence and to determine the factors associated with HSV-2 seropositivity in HIVnegative
high-risk MSM from Rio de Janeiro, Brazil.
Methods: Stored sera were tested to estimate HSV-2 seroprevalence, while socio-demographic
and sexual behavior data were used to measure associations between risk factors and HSV-2
seropositivity. Using the Poisson regression model with robust variance, prevalence ratios (PR)
were used to estimate de degree of association between risk factors and HSV-2 seropositivity in
bivariate and multivariate analyses.
Results: Seroprevalence of HSV-2 was of 45.7% (184 out of 403). Factors independently associated
with HSV-2 seroprevalence in the multivariate model were: older age (≥ 26 years, PR: 1.41 95%
Confidence Interval: 1.11–1.78), non-white race (PR: 1.32 95%CI: 1.06–1.64), positive serology for
syphilis (PR: 1.65 95%CI: 1.33–2.05), positive serology for hepatitis B (PR: 1.25 95%CI: 0.99–1.57),
stable male partner in the past 6 months (PR: 1.42 95%CI: 1.12–1.79), and unprotected anal sex
with a stable female partner (PR: 1.46 95%CI: 1.05–2.04) in the 6 months preceding the crosssectional
assessment.
Conclusion: The present study made evident a high prevalence of HSV-2 infection in a sample of
HIV-negative high-risk MSM from Rio de Janeiro. This finding indicates the need and urgency for
implementing integrated programs for the prevention of HSV-2 and other sexually transmitted
diseases, and, in particular, programs targeting high-risk MSM
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