Comportamento geotécnico de misturas granulometricas de solo-grits

Neste artigo, analisou-se a influência das diversas frações granulométricas do resíduo grits nos parâmetros ótimos de compactação, resistência mecânica e expansão, quando em misturas com dois solos típicos da Zona da Mata Norte de Minas Gerais, Brasil, com fins de aplicação em estradas florestais. Os teores de resíduo empregados nas misturas foram de 4, 8, 12, 16, 20, 24 e 28%, em relação à massa seca de solos, trabalhando-se com as energias de compactação dos ensaios Proctor intermediário e modificado. As frações de resíduo estudadas foram as equivalentes a argila e silte (Ø < 0,074 mm), areia (0,074 mm < Ø < 2,0 mm) e pedregulho (2,0 mm< Ø < 76 mm), considerando-se a escala granulométrica adotada pelo DNIT (1996). Fez-se uso do ensaio de CBR para avaliação da capacidade de suporte e expansão dos solos e misturas. Os resultados indicaram que a fração fina do grits é a que mais contribui para ganhos de resistência mecânica, o que evidencia a sua importância na reatividade das misturas, sendo a fração pedregulho a menos influente no ganho de capacidade de suporte dos solos.

Efeitos da cultura da cevada e de períodos de controle sobre o crescimento e produção de sementes de Raphanus sativus L.

Este experimento teve por objetivo avaliar os efeitos da cultura da cevada e de períodos de controle das plantas daninhas sobre o crescimento e produção de sementes de Raphanus sativus. Foram considerados dois tratamentos testemunha sem controle das plantas daninhas, com e sem a cultura. Nos oito demais tratamentos, a cultura esteve sempre presente, controlando-se as plantas daninhas até 10, 20, 30, 40, 50, 60, 80 e 100 dias após a emergência da cevada. A comunidade infestante da área era composta quase exclusivamente por R. .sativus. Avaliou-se o número de plantas, acúmulos de matéria seca, número médio de frutos e sementes de nabiça por planta e por unidade de área ; foram ainda avaliados o número médio de sementes por fruto, peso médio de 1.000 sementes e a contribuição das sementes na composição da matéria se catota. A análise dos resultados evidenciou que a espécie Raphanus sativus apresenta elevado potencial reprodutivo, sendo possível concluir pela ineficiência de programas de controle de curta duração, em termos de redução do banco de sementes. A presença da cultura da cevada reduziu tanto o crescimento quanto o número de sementes produzidas pela nabiça (R. sativus). Na ausência da cultura e de práticas de controle foram produzidas 5.074 sementes/m, a partir de 125 plantas/m ainda presentes na colheita da cultura.

Anti-leishmania antibodies in cerebrospinal fluid from dogs with visceral leishmaniasis

Visceral leishmaniasis in Brazil is caused by Leishmania (Leishmania) chagasi and the dog is its most important reservoir. The clinical features in dogs include loss of weight, lymphadenopathy, renal failure, skin lesions, fever, hypergammaglobulinemia, hepatosplenomegaly, anemia, and, rarely, neurological symptoms. Most infected animals develop active disease, characterized by high anti-leishmania antibody titers and depressed lymphoproliferative ability. Antibody production is not primarily important for protection but might be involved in the pathogenesis of tissue lesions. An ELISA test was used to determine if there is an association between neurological symptoms and the presence of anti-L. chagasi antibodies in cerebrospinal fluid (CSF). Thirty serum and CSF samples from symptomatic mixed breed dogs (three with neurological symptoms) from a region of high incidence of visceral leishmaniasis in Brazil were examined for antibody using total parasite antigen and anti-dog IgG peroxidase conjugate. A high level of L. chagasi antibodies was observed in sera (mean absorbance ± SD, 1.939 ± 0.405; negative control, N = 20, 0.154 ± 0.074) and CSF (1.571 ± 0.532; negative control, N = 10, 0.0195 ± 0.040) from all animals studied. This observation suggests that L. chagasi can cause breakdown of filtration barriers and the transfer of antibodies and antigens from the blood to the CSF compartment. No correlation was observed between antibody titer in CSF and neurological symptoms.

Molecular and cellular pathogenesis of autosomal recessive polycystic kidney disease

Autosomal recessive polycystic kidney disease (ARPKD) is an inherited disease characterized by a malformation complex which includes cystically dilated tubules in the kidneys and ductal plate malformation in the liver. The disorder is observed primarily in infancy and childhood, being responsible for significant pediatric morbidity and mortality. All typical forms of ARPKD are caused by mutations in a single gene, PKHD1 (polycystic kidney and hepatic disease 1). This gene has a minimum of 86 exons, assembled into multiple differentially spliced transcripts and has its highest level of expression in kidney, pancreas and liver. Mutational analyses revealed that all patients with both mutations associated with truncation of the longest open reading frame-encoded protein displayed the severe phenotype. This product, polyductin, is a 4,074-amino acid protein expressed in the cytoplasm, plasma membrane and primary apical cilia, a structure that has been implicated in the pathogenesis of different polycystic kidney diseases. In fact, cholangiocytes isolated from an ARPKD rat model develop shorter and dysmorphic cilia, suggesting polyductin to be important for normal ciliary morphology. Polyductin seems also to participate in tubule morphogenesis and cell mitotic orientation along the tubular axis. The recent advances in the understanding of in vitro and animal models of polycystic kidney diseases have shed light on the molecular and cellular mechanisms of cyst formation and progression, allowing the initiation of therapeutic strategy designing and promising perspectives for ARPKD patients. It is notable that vasopressin V2 receptor antagonists can inhibit/halt the renal cystic disease progression in an orthologous rat model of human ARPKD.

There is no difference in hepatic fibrosis rates of patients infected with hepatitis C virus and those co-infected with HIV

Some studies have suggested that human immunodeficiency virus (HIV) infection modifies the natural history of hepatitis C virus (HCV) infection, accelerating the progression of fibrosis and the development of cirrhosis. Our objective was to evaluate the fibrosis progression rate (FPR) in HCV/HIV-co-infected patients, and to identify factors that may influence it. HCV-mono-infected and HCV/HIV-co-infected patients with a known date of HCV infection (transfusion or injection drug use) and a liver biopsy were included. The FPR was defined as the ratio between the fibrosis stage (Metavir score) and the estimated length of infection in years and the result was reported as fibrosis units per year. The factors studied were gender, age at infection, consumption of alcohol, aminotransferase levels, histological activity grade, HCV genotype and viral load, CD4 cell count, HIV viral load, and the use of antiretroviral therapy. Sixty-five HCV-infected (group 1) and 53 HCV/HIV-co-infected (group 2) patients were evaluated over a period of 19 months. The mean FPR of groups 1 and 2 was 0.086 ± 0.074 and 0.109 ± 0.098 fibrosis units per year, respectively (P = 0.276). There was a correlation between length of HCV infection and stage of fibrosis in both groups. The age at infection, the aspartate aminotransferase level (r = 0.36) and the inflammatory activity grade were correlated with the FPR (P < 0.001). No difference in FPR was found between HCV-mono-infected and HCV/HIV-co-infected patients.