999 resultados para Angiotensin III


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Expone los resultados del análisis de las muestras de zooplancton colectados frente al Perú, para cumplir uno de los objetivos, la obtención de huevos y larvas de peces y Myctophidoe en diversas fases de desarrollo.

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Entre els dies 13 i 17 de novembre de 2002 va tenir lloc a la ciutat de Sevilla el III Congrés Ibèric sobre Gestió i Planificació de l’Aigua, que, en aquesta ocasió, portava per títol «La Directiva Marc de l’Aigua: realitats i futurs». El congrés fou organitzat per la Fundación Nueva Cultura del Agua, amb la col•laboració de la Universidad de Sevilla i d’una àmplia sèrie d’institucions relacionades amb la investigació o gestió d’aquest recurs. Considerant l’anàlisi i la diagnosi de la situació actual contingudes a les edicions anteriors (Saragossa 1998 i Porto 2000) i l’ampli debat dels últims anys, el III Congrés Ibèric es caracteritza per un plantejament d’avenç i propostes i per incloure alguns dels aspectes de la política de l’aigua menys atesos fins aleshores

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En aquest treball d’investigació, s’estudiaran nanopartícules magnètiques concretament nanopartícules de magnetita (Fe3O4) on a partir de diferents precursors i amb unes condicions determinades es poden variar la seva forma i la seva mida. Aquestes mides i formes diferents són molt útils a l’hora d’introduir-les dins d’una solució de precursor del material superconductor ceràmic YBa2Cu3O7-δ (YBCO) ja que es produeix un augment significatiu de la densitat de corrent crítica. El mètode sintètic utilitzat en aquests treball d’investigació, és l’anomenat descomposició tèrmica, que ens permet sintetitzar nanopartícules de magnetita amb el corresponent control de mida i de forma desitjats.

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Collection : Bibliothèque pour tous

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There are only a few studies on the ontogeny and differentiation process of the hypothalamic supraoptic-paraventriculo-neurohypophysial neurosecretory system. In vitro neuron survival improves if cells are of embryonic origin; however, surviving hypothalamic neurons in culture were found to express small and minimal amounts of arginine-vasopressin (AVP) and oxytocin (OT), respectively. The aim of this study was to develop a primary neuronal culture design applicable to the study of magnocellular hypothalamic system functionality. For this purpose, a primary neuronal culture was set up after mechanical dissociation of sterile hypothalamic blocks from 17-day-old Sprague-Dawley rat embryos (E17) of both sexes. Isolated hypothalamic cells were cultured with supplemented (B27)-NeuroBasal medium containing an agent inhibiting non-neuron cell proliferation. The neurosecretory process was characterized by detecting AVP and OT secreted into the medium on different days of culture. Data indicate that spontaneous AVP and OT release occurred in a culture day-dependent fashion, being maximal on day 13 for AVP, and on day 10 for OT. Interestingly, brain-derived neurotrophic factor (BDNF) and Angiotensin II (A II) were able to positively modulate neuropeptide output. Furthermore, on day 17 of culture, non-specific (high-KCl) and specific (Angiotensin II) stimuli were able to significantly (P < 0.05) enhance the secretion of both neuropeptides over respective baselines. This study suggests that our experimental design is useful for the study of AVP- and OT-ergic neuron functionality and that BDNF and A II are positive modulators of embryonic hypothalamic cell development.

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O objetivo principal deste trabalho foi analisar a variação dos fatores de retardamento (R) e dos coeficientes de dispersão-difusão (D) para o crômio (III) em dois solos muito intemperizados, considerando diferentes atributos edáficos: textura, pH e matéria orgânica. Utilizaram-se amostras dos horizontes A e B com diferença marcante no teor de matéria orgânica de dois solos coletados no estado de São Paulo: Latossolo Vermelho eutroférrico textura argilosa (LVe) e Latossolo Vermelho-Amarelo distrófico textura média (LVd). A alteração do pH das amostras do horizonte superficial foi realizada com adição de carbonato de cálcio para elevar a saturação por bases a 70%. Foram realizados experimentos de adsorção em condições estáticas e de lixiviação em colunas de solo, utilizando a teoria do deslocamento miscível. Os Rs obtidos para o LVe foram maiores em comparação aos obtidos para o LVd. O aumento do pH do solo propiciado pela adição de carbonato de cálcio resultou em aumento no R. No LVe, a presença significativa de ácidos fúlvicos na matéria orgânica propiciou um R menor no horizonte superficial em relação ao subsuperficial. Não foi evidenciada relação nítida entre D e os diferentes solos, níveis de calagem e horizontes.

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This study was conducted to assess the pharmacologic properties of the new orally active angiotensin II subtype I (AT1) antagonist UR-7247, a product with a half-life >100 h in humans. The experiment was designed as an open-label, single-dose administration study with four parallel groups of four healthy men receiving increasing single oral doses (2.5, 5, and 10 mg) of UR-7247 or losartan, 100 mg. Angiotensin II receptor blockade was investigated < or =96 h after drug intake, with three independent methods [i.e., the inhibition of blood pressure (BP) response to exogenous Ang II, an in vitro Ang II-receptor assay (RRA), and the reactive increase in plasma angiotensin II. Plasma drug levels also were measured. The degree of blockade observed in vivo was statistically significant < or = 96 h with all UR-7247 doses for diastolic BP (p < 0.05) and < or =48 h for systolic BP. The maximal inhibition achieved with 10 mg UR-7247 was measured 6-24 h after drug intake and reached 54 +/- 17% and 48 +/- 20% for diastolic and systolic responses, respectively. Losartan, 100 mg, induced a greater short-term AT1-receptor blockade than 2.5- and 5.0-mg doses of UR-7247 (p < 0.001 for diastolic BP), but the UR-7247 effect was longer lasting. In vivo, no significant difference was observed between 10 mg UR-7247 and 100 mg losartan 4 h after drug intake, but in vitro, the blockade achieved with 100 mg losartan was higher than that seen with UR-7247. Finally, the results confirm that UR-7247 has a very long plasma elimination half-life, which may be due to a high but also tight binding to protein binding sites. In conclusion, UR-7247 is a long-lasting, well-tolerated AT1 receptor in healthy subjects.