Investigação da memória autobiográfica em idosos com demência de Alzheimer nas fases leve e moderada

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Remoção de frações de óleo leve e pesado de rocha calcária através de sistemas microemulsionados

In this research the removal of light and heavy oil from disintegrated limestone was investigated with use of microemulsions. These chemical systems were composed by surfactant, cosurfactant, oil phase and aqueous phase. In the studied systems, three points in the water -rich microemulsion region of the phase diagrams were used in oil removal experiments. These microemulsion systems were characterized to evaluate the influence of particle size, surface tension, density and viscosity in micellar stability and to understand how the physical properties can influence the oil recovery process. The limestone rock sample was characterized by thermogravimetry, BET area, scanning electron microscopy and X-ray fluorescence. After preparation, the rock was placed in contact with light and heavy oil solutions to allow oil adsorption. The removal tests were performed to evaluate the influence of contact time (1 minute, 30 minutes, 60 minutes and 120 minutes), the concentration of active matter (20, 30 and 40 %), different cosurfactants and different oil phases. For the heavy oil, the best result was on SME 1, with 20 % of active matter, 1 minute of contact time, with efficiency of 93,33 %. For the light oil, also the SME 1, with 20 % of active matter, 120 minutes of contact time, with 62,38 % of efficiency. From the obtained results, it was possible to conclude that microemulsions can be considered as efficient chemical systems for oil removal from limestone formations

Efeitos do sistema de condução, poda e irrigação na produção do maracujazeiro doce

O maracujá é um fruto de ampla aceitação dada a qualidade de seu suco, sendo o maracujazeiro-amarelo o mais cultivado no Brasil. Nos últimos anos, cresceu o interesse pelo maracujazeiro doce, em função de alcançar bons preços no mercado in natura. Assim, informações técnicas por parte dos agricultores têm se intensificado. Este trabalho teve como objetivo avaliar a produção e a qualidade dos frutos desta espécie, cultivada sob poda e irrigação em diferentes sistemas de condução. O experimento foi conduzido no delineamento em faixas, contendo 12 tratamentos (plantas com e sem irrigação, com e sem poda e três sistemas de condução) e 3 repetições. Com base nos resultados obtidos, pode-se concluir: a) o sistema de condução e a poda não afetaram o tamanho dos frutos; b) o sistema de condução não afetou a massa dos frutos, porém as plantas podadas produziram frutos com maior massa; c) a poda diminuiu o número de frutos por planta e o rendimento por área, nos sistemas de condução em T normal e espaldeira vertical com um fio de arame; d) a poda não alterou o número de frutos por planta e o rendimento por área, no sistema de condução em espaldeira vertical com dois fios de arame.

Poda apical, densidade de plantas e cobertura plástica do solo na produtividade do tomateiro em cultivo protegido

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Capacidade de enraizamento de variedades de nespereira submetidas à poda de renovação

O presente trabalho avaliou a capacidade de enraizamento de cinco variedades de nespereira (Eriobotrya japonica Lindl.), sendo Champagne, Precoce de Itaquera, Mizuho, Mogui e Tanaka, obtidas pela poda de renovação. Estacas tenras apicais, contendo um par de folhas e cerca de 15 cm, foram tratadas por cinco segundos com ácido indolbutírico (IBA) (0; 1.000; 3.000; 5.000 e 7.000 mg.L-1). O experimento foi conduzido em câmara de nebulização intermitente pertencente à UNESP/FCAV (21º15'22 S e 48º18'58 W). O delineamento experimental foi inteiramente casualizado, em esquema fatorial 5x5 (5 variedades e 5 concentrações de IBA), com 4 repetições e 10 estacas por parcela. As avaliações foram feitas após 90 dias. Os resultados indicaram um incremento de enraizamento e número de raízes crescente com a concentração de IBA utilizada, com exceção da variedade Mogui, que apresentou melhores resultados apenas quanto ao comprimento de raízes. Posterior ao transplantio, a sobrevivência das mudas foi alta (90%), apresentando condições de serem plantadas no campo, aos seis meses, ou de serem enxertadas aos oito meses, decorrido desde o estaqueamento.

Produção e qualidade de frutos da goiabeira 'Paluma', submetida à diferentes épocas de poda em clima subtropical

O objetivo deste trabalho foi avaliar a produção e a qualidade dos frutos da goiabeira 'Paluma' com cinco anos de idade, submetida a podas drásticas, em diferentes meses, na Fazenda Experimental São Manuel FCA/UNESP, Campus de Botucatu-SP. O delineamento experimental foi o inteiramente casualizado, com quatro tratamentos e dez repetições, com uma planta útil por parcela experimental, completamente rodeada por quatro plantas na bordadura. Os tratamentos corresponderam aos seguintes meses de poda: T1: sem poda (testemunha), T2: poda em agosto, T3: poda em setembro e T4: poda em outubro. As características avaliadas foram: número, peso médio, diâmetros longitudinal e transversal dos frutos, produção por planta, produtividade, teores de sólidos solúveis (SS), acidez titulável (AT), relação SS/AT e pH. Com relação ao número de dias entre o início e o final das colheitas (período produtivo), observou-se que a poda, independentemente da época, favoreceu o aumento do intervalo de produção. As goiabeiras submetidas à poda em agosto apresentaram maiores valores de número médio de frutos (385) e de produção por planta (58,82 kg planta-1), diferindo das outras épocas. Os teores de sólidos solúveis, acidez titulável, pH e relação SS/AT dos frutos não foram influenciados pelas épocas de realização da poda.

ESTUDO COMPARATIVO DUPLO-CEGO DA EFICACIA E SEGURANCA DO CILAZAPRIL COMPARADAS A NIFEDIPINE 'RETARD' NO TRATAMENTO DA HIPERTENSAO ARTERIAL LEVE E MODERADA

Purpose: To evaluate the antihypertensive efficacy and safety of cilazapril compared to nifedipine retard in mild to moderate hypertension. Methods: Forty randomized out-patients with mild moderate hypertension, diastolic pressure (DP) between 95 and 115 mmg/Hg, with placebo for 15 days were randomized and allocated for treatment, double-blind, once daily with cilazapril 2.5 mg (n = 20) or nifedipine retard 20 mg (20 = n) for four weeks. The non-responders (DP > 90 mmHg) had the dosage increased twice, b.i.d., while responders were maintained up to 10 weeks. Clinical visits were performed before, at baseline and every two weeks and the laboratory test was performed after placebo run-in, 4th and 10th weeks of treatment. Results: The blood pressure (BP) were similar between groups at the end of the placebo (cilazapril 151 ± 14/103 ± 5 - nifedipine 157 ± 17/108 ± 7 mmHg, p > 0.05). DP decreased already at second weeks (cilazapril 95 ± 9 - nifedipine 96 ± 11 mmHg, p < 0.05, compared to week 0) in both groups at the end of study with no differences inter groups. BP normalization was obtained in 58% of the patients with cilazapril and in 61% in the nifedipine group. Adverse biochemical effects were not observed in any group. Six (16%) patients of the cilazapril and 15 (39%) of nifedipine related collateral events, although no difference were observed between groups. Conclusion: Cilazapril 2.5 to 5 mg normalized BP in 58% of mild and moderate hypertension patients, and this efficacy was similar to sustained-release nifedipine 20 to 40 mg. Cilazapril had no adverse effects on the biochemical parameters with low incidence of collateral effects.

TRATAMENTO DA HIPERTENSAO ARTERIAL LEVE E MODERADA COM FOSINOPRIL. COMPARACAO DE EFEITOS ADVERSOS COM OUTROS ANTI-HIPERTENSIVOS

Purpose - To evaluate the adverse reactions of fosinopril with other antihypertensives used as monotherapy. Methods - Out-patients (n = 2,568) with diagnostic of mild to moderate hypertension, diastolic blood pressure (DBP) 95-115 mmHg, with no antihypertensive treatment for 15 days, were included to treatment initially with fosinopril (F) 10mg, once daily, for six weeks. After this period, patients with DBP >95mmHg had the dosage, once daily, increased to 20 mg, while the others were maintained with the same dosage for six more weeks. Adverse reactions of 822 patients treated as monotherapy were grouped as absent, musculoskeletal, cardiovascular, cough, gastrointestinal, neurological, genital-urinary dysfunctions and dermatological and compared with 1,568 with F. Monotherapy consist in α-methyldopa (100 patients); β-blocker (129); calcium blocker (106); diuretic (394); and another ACE inhibitors (93). Results - At the end of the period without treatment, the blood pressure (BP), 165 ± 16/105 ± 7 mmHg decreased significantly at 6(th) week to 144 ± 15/91 ± 9 mmHg (p < 0.05 vs week 0) with further lowering to 139 ± 13/86 ± 7 mmHg till the end of 12(th) week. BP response (DBP ≤90 mmHg) was obtained in 89% of the patients with F. Absence of adverse reactions were ≥70% in patients with F compared to other drugs. Conclusion - Fosinopril has demonstrated therapeutic efficacy and less adverse reactions compared to antihypertensives used previously as monotherapy.

EFICACIA E TOLERABILIDADE DA ASSOCIACAO CAPTOPRIL + HIDROCLOROTIAZIDA NO TRATAMENTO DA HIPERTENSAO ARTERIAL LEVE A MODERADA. ESTUDO MULTICENTRICO

Purpose. To evaluate the antihypertensive efficacy and tolerability of captopril 50 mg + hydrochlorothiazide 25 mg daily in mild to moderate primary hypertension. Methods. Out-patients (n = 471) with mild to moderate hypertension, diastolic blood pressure (DBP) 95-115 mmHg, with 15 days of washout, were included to the treatment initially with half tablet of the association of captopril 50 mg + hydrochlorothiazide 25 mg once daily, for 30 days. After this period, patients with DBP > 90 mmHg had the dosage duplicated, while the others had the same dosage for 60 days more. Evaluation was performed 15 days before and then every month during active drug. Results. Twenty six patients were withdrawn, 13 (2,7%) by adverse effects and 13 by protocol violation. At the end of the wash-out period, the blood pressure (BP), 162 ± 16/103 ± 6 mmHg decreased significantly at the 30th day to 146 ± 14/92 ± 8 mmHg (p < 0,001 vs 0th day); 139 ± 12/86 ± 7 mmHg at the 60th day, (p < 0,001 vs 30th day), and further to 136 ± 11/84 ± 5 mmHg (p < 0,001 vs day 0) till the end of the 90th day. Antihypertensive efficay (DBP ≤ 90 mmHg and decreased for the DBP ≥ 10 mmHg) was obtained in 82% of the patients. There was no difference in BP control considering race, hypertension level, previous antihypertensive treatment and obesity. Cough (4%) was the main adverse event. Conclusion. Captopril + hydrochlorothiazide was effective and safe in the treatment of mild to moderate hypertension. The favorable response was observed in 82% of the patients independently of race, hypertensive level, previous antihypertensive treatment and obesity. Low incidence of side effects was reported, with no difference from others reported in the literature.

Avaliação estatística de métodos de poda aplicados em neurônios intermediários da rede neural MLP

There are several papers on pruning methods in the artificial neural networks area. However, with rare exceptions, none of them presents an appropriate statistical evaluation of such methods. In this article, we proved statistically the ability of some methods to reduce the number of neurons of the hidden layer of a multilayer perceptron neural network (MLP), and to maintain the same landing of classification error of the initial net. They are evaluated seven pruning methods. The experimental investigation was accomplished on five groups of generated data and in two groups of real data. Three variables were accompanied in the study: apparent classification error rate in the test group (REA); number of hidden neurons, obtained after the application of the pruning method; and number of training/retraining epochs, to evaluate the computational effort. The non-parametric Friedman's test was used to do the statistical analysis.

Sertralina no tratamento de pacientes com depressão maior leve e moderada: Estudo multicêntrico brasileiro

Introduction: To evaluate the efficacy, safety, and tolerability of sertraline for the treatment of Brazilian patients with mild to moderate major depression. Patients and methods: Patients were 18 years old or older treated on an out-patient basis. Previous medications were stopped for a 2-week washout period. Afterwards, patients received sertraline, initial dose of 50 mg/day up to the 4 th week. The dose could then be increased up to 200 mg/day according to the efficacy and tolerability. Therapeutic efficacy was evaluated with the Montgomery-Asberg Depression Rating Scale (MADRS), Hamilton scale for depression (HAM-D), and Clinical Global Impression (CGI). Results: 51 patients (42 women) were evaluated regarding efficacy and safety. Treatment with sertraline significantly decreased scores of MADRS, HAM-D e ICGfrom 15.7 ± 6.1; 12.2 ± 3.9 e 3.5 ± 0.6 to 6.2 ± 6.5; 5.4 ± 4.7 e 2.3 ± 1.0 (P < 0.0001), respectively. Sertraline was well tolerated. Gastro-intestinal upset (N=14; 24.6%), headache (N=7; 12.3%), sleep alterations (H-7; 12.3%), dizziness (N-4; 7.0%), and anorexia (N=4; 7.0%) were the most common adverse events. Six patients discontinued the treatment due to adverse events. Conclusion: Sertraline is efficient and presents a favorable safety and tolerability profile for the treatment of Brazilian patients with mild to moderate major depression. © Copyright Moreira Jr. Editora.