975 resultados para VEGETAL TISSUES


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Nickel, although essential to plants, may be toxic to plants and animals. It is mainly assimilated by food ingestion. However, information about the average levels of elements (including Ni) in edible vegetables from different regions is still scarce in Brazil. The objectives of this study were to: (a) evaluate and optimize a method for preparation of vegetable tissue samples for Ni determination; (b) optimize the analytical procedures for determination by Flame Atomic Absorption Spectrometry (FAAS) and by Electrothermal Atomic Absorption (ETAAS) in vegetable samples and (c) determine the Ni concentration in vegetables consumed in the cities of Lorena and Taubaté in the Vale do Paraíba, State of São Paulo, Brazil. By means of the analytical technique for determination by ETAAS or FAAS, the results were validated by the test of analyte addition and recovery. The most viable method tested for quantification of this element was HClO4-HNO3 wet digestion. All samples but carrot tissue collected in Lorena contained Ni levels above the permitted by the Brazilian Ministry of Health. The most disturbing results, requiring more detailed studies, were the Ni concentrations measured in carrot samples from Taubaté, where levels were five times higher than permitted by Brazilian regulations.

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Many mucosal pathogens invade the host by initially infecting the organized mucosa-associated lymphoid tissue (o-MALT) such as Peyer's patches or nasal cavity-associated lymphoid tissue (NALT) before spreading systemically. There is no clear demonstration that serum antibodies can prevent infections in o-MALT. We have tested this possibility by using the mouse mammary tumor virus (MMTV) as a model system. In peripheral lymph nodes or in Peyer's patches or NALT, MMTV initially infects B lymphocytes, which as a consequence express a superantigen (SAg) activity. The SAg molecule induces the local activation of a subset of T cells within 6 days after MMTV infection. We report that similar levels of anti-SAg antibody (immunoglobulin G) in serum were potent inhibitors of the SAg-induced T-cell response both in peripheral lymph nodes and in Peyer's patches or NALT. This result clearly demonstrates that systemic antibodies can gain access to Peyer's patches or NALT.

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A contaminação de solos por chumbo representa importante risco à saúde humana, sendo o município de Santo Amaro da Purificação, BA, um dos mais graves casos de contaminação do metal. O objetivo deste trabalho foi avaliar o efeito de ácidos húmicos e carvão vegetal ativado como amenizantes da toxidez de Pb para plantas de milho cultivadas em solo contaminado, coletado próximo à área da metalúrgica responsável pela contaminação. As doses foram estabelecidas com base no teor de C dos materiais (ácidos húmicos de compostagem, ácidos húmicos comerciais e carvão vegetal) e corresponderam a 0; 0,75; 1,5; 3; e 7,5 g kg-1 de C no solo. Ao final de 43 dias de cultivo, as plantas foram coletadas rente ao solo, separadas em parte aérea e raízes e submetidas à digestão nítrico perclórica para determinação de Pb. A fim de avaliar o efeito do metal sobre o aparato fotossintético, os teores de clorofilas a e b foram também avaliados. Os amenizantes aplicados no solo contaminado foram eficientes em diminuir o estresse provocado por Pb nas plantas de milho, sendo a maior eficiência obtida para os ácidos húmicos de compostagem, seguida pelo carvão vegetal e pelos ácidos húmicos comerciais. Todos os amenizantes testados diminuíram a translocação de Pb para a parte aérea das plantas, o que implica em maior fixação do metal no solo, com consequente diminuição dos riscos de transferência à cadeia trófica. Por essa razão, esses amenizantes podem ser recomendados para programas de fitoestabilização de Pb em solos.

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In comparison with other micronutrients, the levels of nickel (Ni) available in soils and plant tissues are very low, making quantification very difficult. The objective of this paper is to present optimized determination methods of Ni availability in soils by extractants and total content in plant tissues for routine commercial laboratory analyses. Samples of natural and agricultural soils were processed and analyzed by Mehlich-1 extraction and by DTPA. To quantify Ni in the plant tissues, samples were digested with nitric acid in a closed system in a microwave oven. The measurement was performed by inductively coupled plasma/optical emission spectrometry (ICP-OES). There was a positive and significant correlation between the levels of available Ni in the soils subjected to Mehlich-1 and DTPA extraction, while for plant tissue samples the Ni levels recovered were high and similar to the reference materials. The availability of Ni in some of the natural soil and plant tissue samples were lower than the limits of quantification. Concentrations of this micronutrient were higher in the soil samples in which Ni had been applied. Nickel concentration differed in the plant parts analyzed, with highest levels in the grains of soybean. The grain, in comparison with the shoot and leaf concentrations, were better correlated with the soil available levels for both extractants. The methods described in this article were efficient in quantifying Ni and can be used for routine laboratory analysis of soils and plant tissues.

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PURPOSE: To objectively characterize different heart tissues from functional and viability images provided by composite-strain-encoding (C-SENC) MRI. MATERIALS AND METHODS: C-SENC is a new MRI technique for simultaneously acquiring cardiac functional and viability images. In this work, an unsupervised multi-stage fuzzy clustering method is proposed to identify different heart tissues in the C-SENC images. The method is based on sequential application of the fuzzy c-means (FCM) and iterative self-organizing data (ISODATA) clustering algorithms. The proposed method is tested on simulated heart images and on images from nine patients with and without myocardial infarction (MI). The resulting clustered images are compared with MRI delayed-enhancement (DE) viability images for determining MI. Also, Bland-Altman analysis is conducted between the two methods. RESULTS: Normal myocardium, infarcted myocardium, and blood are correctly identified using the proposed method. The clustered images correctly identified 90 +/- 4% of the pixels defined as infarct in the DE images. In addition, 89 +/- 5% of the pixels defined as infarct in the clustered images were also defined as infarct in DE images. The Bland-Altman results show no bias between the two methods in identifying MI. CONCLUSION: The proposed technique allows for objectively identifying divergent heart tissues, which would be potentially important for clinical decision-making in patients with MI.

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Background: Current methodology of gene expression analysis limits the possibilities of comparison between cells/tissues of organs in which cell size and/or number changes as a consequence of the study (e.g. starvation). A method relating the abundance of specific mRNA copies per cell may allow direct comparison or different organs and/or changing physiological conditions. Methods: With a number of selected genes, we analysed the relationship of the number of bases and the fluorescence recorded at a present level using cDNA standards. A lineal relationship was found between the final number of bases and the length of the transcript. The constants of this equation and those of the relationship between fluorescence and number of bases in cDNA were determined and a general equation linking the length of the transcript and the initial number of copies of mRNA was deduced for a given pre-established fluorescence setting. This allowed the calculation of the concentration of the corresponding mRNAs per g of tissue. The inclusion of tissue RNA and the DNA content per cell, allowed the calculation of the mRNA copies per cell. Results: The application of this procedure to six genes: Arbp, cyclophilin, ChREBP, T4 deiodinase 2, acetyl-CoA carboxylase 1 and IRS-1, in liver and retroperitoneal adipose tissue of food-restricted rats allowed precise measures of their changes irrespective of the shrinking of the tissue, the loss of cells or changes in cell size, factors that deeply complicate the comparison between changing tissue conditions. The percentage results obtained with the present methods were essentially the same obtained with the delta-delta procedure and with individual cDNA standard curve quantitative RT-PCR estimation. Conclusion: The method presented allows the comparison (i.e. as copies of mRNA per cell) between different genes and tissues, establishing the degree of abundance of the different molecular species tested.

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MicroRNAs (miRNAs) are short non-coding RNA molecules playing regulatory roles by repressing translation or cleaving RNA transcripts. Although the number of verified human miRNA is still expanding, only few have been functionally described. However, emerging evidences suggest the potential involvement of altered regulation of miRNA in pathogenesis of cancers and these genes are thought to function as both tumours suppressor and oncogenes. In our study, we examined by Real-Time PCR the expression of 156 mature miRNA in colorectal cancer. The analysis by several bioinformatics algorithms of colorectal tumours and adjacent non-neoplastic tissues from patients and colorectal cancer cell lines allowed identifying a group of 13 miRNA whose expression is significantly altered in this tumor. The most significantly deregulated miRNA being miR-31, miR-96, miR-133b, miR-135b, miR-145, and miR-183. In addition, the expression level of miR-31 was correlated with the stage of CRC tumor. Our results suggest that miRNA expression profile could have relevance to the biological and clinical behavior of colorectal neoplasia.

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Background Plant hormones play a pivotal role in several physiological processes during a plant's life cycle, from germination to senescence, and the determination of endogenous concentrations of hormones is essential to elucidate the role of a particular hormone in any physiological process. Availability of a sensitive and rapid method to quantify multiple classes of hormones simultaneously will greatly facilitate the investigation of signaling networks in controlling specific developmental pathways and physiological responses. Due to the presence of hormones at very low concentrations in plant tissues (10-9 M to 10-6 M) and their different chemistries, the development of a high-throughput and comprehensive method for the determination of hormones is challenging. Results The present work reports a rapid, specific and sensitive method using ultrahigh-performance liquid chromatography coupled to electrospray ionization tandem spectrometry (UPLC/ESI-MS/MS) to analyze quantitatively the major hormones found in plant tissues within six minutes, including auxins, cytokinins, gibberellins, abscisic acid, 1-amino-cyclopropane-1-carboxyic acid (the ethylene precursor), jasmonic acid and salicylic acid. Sample preparation, extraction procedures and UPLC-MS/MS conditions were optimized for the determination of all plant hormones and are summarized in a schematic extraction diagram for the analysis of small amounts of plant material without time-consuming additional steps such as purification, sample drying or re-suspension. Conclusions This new method is applicable to the analysis of dynamic changes in endogenous concentrations of hormones to study plant developmental processes or plant responses to biotic and abiotic stresses in complex tissues. An example is shown in which a hormone profiling is obtained from leaves of plants exposed to salt stress in the aromatic plant, Rosmarinus officinalis.

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Ectopic or tertiary lymphoid tissues (TLTs) are often induced at sites of chronic inflammation. They typically contain various hematopoietic cell types, high endothelial venules, and follicular dendritic cells; and are organized in lymph node-like structures. Although fibroblastic stromal cells may play a role in TLT induction and persistence, they have remained poorly defined. Herein, we report that TLTs arising during inflammation in mice and humans in a variety of tissues (eg, pancreas, kidney, liver, and salivary gland) contain stromal cell networks consisting of podoplanin(+) T-zone fibroblastic reticular cells (TRCs), distinct from follicular dendritic cells. Similar to lymph nodes, TRCs were present throughout T-cell-rich areas and had dendritic cells associated with them. They expressed lymphotoxin (LT) β receptor (LTβR), produced CCL21, and formed a functional conduit system. In rat insulin promoter-CXCL13-transgenic pancreas, the maintenance of TRC networks and conduits was partially dependent on LTβR and on lymphoid tissue inducer cells expressing LTβR ligands. In conclusion, TRCs and conduits are hallmarks of secondary lymphoid organs and of well-developed TLTs, in both mice and humans, and are likely to act as important scaffold and organizer cells of the T-cell-rich zone.

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Compararam-se diferentes formas de análise de experimentos em blocos incompletos, abordadas como casos particulares de modelos mistos, quais sejam: (a) análise intrablocos, em que apenas o efeito do erro experimental é suposto aleatório; (b) análise interblocos (látice), com efeitos de blocos supostos aleatórios; (c) análise BLUP, com os efeitos de tratamentos supostos aleatórios, e (d) modelo aleatório. Além disso, montou-se a ANAVA, considerando duas alternativas: (e) usando o quadrado médio de tratamentos ajustados para blocos e o quadrado médio do erro efetivo do látice; (f) tomando as repetições como blocos completos. Um exemplo de análise de um teste de progênies de Eucalyptus grandis (Hill) Maiden ilustra as implicações da escolha dos modelos para fins de seleção e de caracterização genética de populações. Observou-se que em geral o ordenamento dos tratamentos sofreu maiores alterações ao se mudar a alternativa de análise do que as estimativas do progresso esperado pela seleção. Tendência que se reforça com a seleção mais intensa. As formas de análise que consideram a restrição da casualização (blocos incompletos) foram as mais precisas, e dentre estas, a análise BLUP de tratamentos é conceitualmente a melhor, pois os tratamentos eram progênies de polinização livre, sendo a que mais difere da análise usual do látice. Isto indica ser possível minorar os erros de seleção nas análises de blocos incompletos no melhoramento vegetal.

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O desempenho operacional de uma semeadora-adubadora de plantio direto, versão soja e milho, foi avaliado em um Podzólico Vermelho-Amarelo câmbico, fase terraço, e um Latossolo Vermelho-Amarelo, da Zona da Mata de Minas Gerais. A máquina foi testada em três tipos de cobertura do solo e em duas velocidades de trabalho. Por ocasião do plantio, foram avaliados a patinagem do trator e da semeadora-adubadora, o consumo de combustível e a potência exigida, a distribuição de fertilizante e o nível de danos às sementes. Depois do plantio, foram avaliados o número de sementes distribuídas, o estande final, a profundidade de plantio e a distribuição longitudinal da semente. A uniformidade de distribuição longitudinal foi avaliada pela porcentagem de espaçamentos aceitáveis, distribuição dupla e falhas na distribuição, e pelo coeficiente de variação dos espaçamentos entre sementes. A demanda de potência foi maior no Podzólico, por sua maior densidade e resistência à penetração. Independentemente do tratamento, o número de sementes distribuídas e o estande final não apresentaram diferenças significativas. As sementes distribuídas não tiveram sua qualidade afetada pelos dosadores da máquina. A análise de variância não indicou diferença significativa entre os porcentuais de espaçamentos aceitáveis, a distribuição dupla e as falhas.