Young "healthy" smokers have functional and inflammatory changes in the nasal and the lower airways.

BACKGROUND: Smoking is responsible for most COPD. Although people with COPD often have concomitant nasal disease, there are few studies that report physiologic or inflammatory changes in the upper airways in young asymptomatic smokers. We investigated physiologic and inflammatory changes in the nasal and lower airways of young smokers and if these changes were related to smoking history. METHODS: Seventy-two subjects aged between 18 and 35 years (32 healthy nonsmokers and 40 young smokers) participated in this study. We measured nasal mucociliary clearance (MCC), nasal mucus surface contact angle, cell counts, myeloperoxidase and cytokine concentrations in nasal lavage fluid, exhaled breath condensate (EBC) pH, and lung function. RESULTS: Smokers had faster MCC, an increased number of cells (macrophages, ciliated cells, and goblet cells), increased lavage myeloperoxidase concentration, and decreased EBC pH compared with nonsmokers. There was a significant inverse relationship between pack-year smoking history and EBC pH. There were no differences in lung function or mucus surface properties comparing smokers to nonsmokers. CONCLUSIONS: Young adult smokers have functional and inflammatory changes in the nasal and lower airways and these correlate with smoking history. However, in these young smokers, smoking history was not associated with pulmonary function decline, probably because it is unlikely that spirometry detects early physiologic changes in the airways. TRIAL REGISTRY: ClinicalTrials.gov; No.: NCT01877291; URL: www.clinicaltrials.gov.

Effects of heavy metals and light levels on the biosynthesis of carotenoids and fatty acids in the macroalgae Gracilaria tenuistipitata (var. liui Zhang & Xia)

We present here the effect of heavy metals and of different light intensities on the biosynthesis of fatty acids and pigments in the macroalga Gracilaria tenuistipitata (var. liui Zhang & Xia). In order to verify the fatty acid content, gas chromatography with flame ionization detection (GC-FID) was employed. Pigments (major carotenoids and chlorophyl-a) were monitored by liquid chromatography with diode array detection (HPLC-DAD). Cultures of G. tenuistipitata were exposed to cadmium (Cd2+, 200 ppb) and copper (Cu2+, 200 ppb), as well as to different light conditions (low light: 100 µmol.photons.m-2.s-1, or high light: 1000 µmol.photons.m-2.s-1). Cd2+ and Cu2+ increased the saturated and monounsaturated fatty acid content [14:0, 16:0, 18:0, 18:1 (n-7) and 18:1 (n-9)] and all major pigments (violaxanthin, antheraxanthin, lutein, zeaxanthin, chlorophyll-a and β-carotene). Both heavy metals decreased the levels of polyunsaturated fatty acids (PUFA) [18:2 (n-6), 18:3 (n-6), 18:5 (n-4), 20:4 (n-6), 20:5 (n-3), 22:6 (n-3)]. G. tenuistipitata cultures were exposed to high light intensity for five days and no statistically significant differences were observed in the content of fatty acids. On the other hand, the levels of pigments rose markedly for chlorophyll-a and all of the carotenoids studied.

Desenvolvimento de técnicas de imunoensaio para detecção de microcistina em amostras ambientais / Development of immunoassay techniques to detect microcystin in environmental samples

A contaminação da água para consumo humano por toxinas produzidas por cianobactérias é um problema de saúde pública e das autoridades em todo o mundo. Microcistina-LR (MCLR) é uma cianotoxina heptapeptídica cíclica que inibe as proteínas fosfatases PP1 E PP2A nos hepatócitos. Microcistinas são produzidas por diversos gêneros de cianobactérias e mais de 70 variações estruturais têm sido caracterizadas em florações naturais. Por serem haptenos, as microcistinas são incapazes de induzir uma resposta imune em animais. Conseqüentemente, foi necessário aplicar métodos de conjugação envolvendo a adição de uma proteína carreadora, mcKLH (cationized Keyhole Limpet Hemocyanin). Portanto, o objetivo inicial desta tese foi o de obter anticorpos monoclonal (em camundongos) e policlonal (em coelho) anti- MCLR. Com relação ao anticorpo monoclonal foram obtidos 9 hibridomas (k₂9, k₂10, k₃17, k₂48, k₂84, k₂90, k₂161, k₂226, k₂232), sendo que apenas 5 se mostraram estáveis (k₂9, k₃17, k₂48, k₂84, k₂232). Estes foram selecionados para serem isotipados, expandidos em líquido ascítico, purificados em coluna cromatográfica de proteína-A e titulados. Dentre estes cinco hibridomas secretores de anticorpos, o clone k₃17 foi o que melhor reconheceu (mais específico) a toxina MCLR. Os anticorpos do sobrenadante de meio de cultura do hibridoma e o fluido ascítico purificado foram identificados pelo ensaio ELISA (Enzyme Linked Immunosorbent Assay) previamente padronizado. Mesmo sensibilizando a placa de ELISA com diferentes antígenos, tais como MCLR-cBSA, MCLR, MCLR, MCRR, MCYR e MCLA, o clone 17 foi o que apresentou melhor linearidade frente às variantes de microcistina. Portanto, o clone 17 (isótipo IgG1) obtido é muito promissor e será usado para detecção de MCLR na água para consumo humano através do...

The contamination of drinking water by cyanobacterial toxins is a public health issue and a concern for water authorities throughout the world. Microcystin-LR (MCLR) is a hazardous cyclic heptapeptide cyanotoxin, which inhibits protein phosphatase PP1 and PP2A in hepatocytes. Microcystins are produced by several genera of cyanobacteria and presents more than 70 structural variations characterized in natural blooms. As haptens, microcystins are unable to invoke an immune response in animals. Consequently, the application of conjugation methods with an additional carrier protein, the KLH (Keyhole Limpet Hemocyanin) was necessary. The main objective of this study was to obtain monoclonal (in mice) and polyclonal (in rabbits) antibodies for reacting against MCLR. In what refers to monoclonal antibodies, 9 hybridomas (k₂9, k₂10, k₃17, k₂48, k₂84, k₂90, k₂161, k₂226, k₂232) were obtained; however only 5 were stables (k₂9, k₃17, k₂48, k₂84, k₂232). These were selected to be isotyped, expanded in ascitic fluid, purified by protein-A column chromatography and then, they were titrated. Out of these five antibody-secretor hybridomas, clone k₃17 was the best to recognize (more specific) the MCLR toxins. Antibodies in hybridoma cell culture supernatant and purified ascites fluid were identified by ELISA assay (Enzyme Linked Immunosorbent Assay) as prior standardized. Even when sensitizing ELISA plate with different antigens, as MCLR-cBSA, MCLR, MCLR, MCRR, MCYR and MCLA, clone 17 presented the best linearity against microcystin variants. Therefore, the obtained clone 17 (isotype IgG1) is a promising clone and shall be used for detecting MCLR in drinking water through the development of a competitive ELISA immunoassay kit. In what refers to the polyclonal antibody, MCLR-mcKLH was used as...