998 resultados para Balneario de Buyeres de Nava (Asturias).
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Se colectaron en diferentes regiones de Cuba semillas de las accesiones de papayo Tallo Morado de Nava, Amarilla de Duaba, Amarilla de Nava y Sapote de Pilón. Estas se plantaron en condiciones de campo en Jagüey Grande, Matanzas - Cuba, donde se evaluó la presencia e intensidad de síntomas de mancha anular, siguiendo una escala graduada del 1 al 5. Los resultados mostraron un incremento temporal de la proporción de plantas afectadas en todas las accesiones. La accesión Amarilla de Duaba mostró los síntomas a los dos meses después de la primera evaluación (MDPE), mientras que el resto lo hizo a los cinco MDPE, aunque con proporciones que variaron entre ellas. A los siete MDPE las accesiones Amarilla de Duaba y Amarilla de Nava mostraron proporciones idénticas de plantas enfermas, mientras que Tallo morado de Nava y Sapote de Pilón mostraron proporciones inferiores. La intensidad de los síntomas se incrementó en los diferentes órganos siguiendo el siguiente orden: tallo (1,7 a 2,66), pecíolos (2,21 a 3,03) y follaje (3,44-4,03). En los frutos la intensidad de los síntomas observados fue inferior a 2,5, considerados como leves de acuerdo a su intensidad y distribución. Se ofrecen los primeros resultados sobre la susceptibilidad a la mancha anular de estas accesiones, siendo de gran utilidad para los productores, así como para los programas de mejoramiento genético en el país.
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A new metalloendopeptidase was purified to apparent homogeneity from a homogenate of normal human liver using successive steps of chromatography on DEAE-cellulose, hydroxyapatite and Sephacryl S-200. The purified enzyme hydrolyzed the Pro7-Phe8 bond of bradykinin and the Ser25-Tyr26 bond of atrial natriuretic peptide. No cleavage was produced in other peptide hormones such as vasopressin, oxytocin or Met- and Leu-enkephalin. This enzyme activity was inhibited by 1 mM divalent cation chelators such as EDTA, EGTA and o-phenanthroline and was insensitive to 1 µM phosphoramidon and captopril, specific inhibitors of neutral endopeptidase (EC 3.4.24.11) and angiotensin-converting enzyme (EC 3.4.15.1), respectively. With Mr 85 kDa, the enzyme exhibits optimal activity at pH 7.5. The high affinity of this endopeptidase for bradykinin (Km = 10 µM) and for atrial natriuretic peptide (Km = 5 µM) suggests that it may play a physiological role in the inactivation of these circulating hypotensive peptide hormones.
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The serious neuropsychological repercussions of hepatic encephalopathy have led to the creation of several experimental models in order to better understand the pathogenesis of the disease. In the present investigation, two possible causes of hepatic encephalopathy, cholestasis and portal hypertension, were chosen to study the behavioral impairments caused by the disease using an object recognition task. This working memory test is based on a paradigm of spontaneous delayed non-matching to sample and was performed 60 days after surgery. Male Wistar rats (225-250 g) were divided into three groups: two experimental groups, microsurgical cholestasis (N = 20) and extrahepatic portal hypertension (N = 20), and a control group (N = 20). A mild alteration of the recognition memory occurred in rats with cholestasis compared to control rats and portal hypertensive rats. The latter group showed the poorest performance on the basis of the behavioral indexes tested. In particular, only the control group spent significantly more time exploring novel objects compared to familiar ones (P < 0.001). In addition, the portal hypertension group spent the shortest time exploring both the novel and familiar objects (P < 0.001). These results suggest that the existence of portosystemic collateral circulation per se may be responsible for subclinical encephalopathy.
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To further understand in vivo localization and trafficking of a-tocopherol (a-Toe), the most biologically active form of vitamin E, between lipid environments, tocopherols are required that can be followed by teclu1iques such as confocal microscopy and fluorescence resonance energy transfer (FRET) assays. To this end, sixteen fluorescent analogues of a-tocopherol (la-d [(1)anthroy loxy -a-tocopherols, A O-a-Toes], 2a-d [w-nitro benzoxadiazole-a-tocopherols, NBD-aToes], 3a-d [w-dansyl-a-tocopherols, DAN-a-Toes], and 4a-d [w-N-methylanthranilamide-atocopherols, NMA-a-TocsD were prepared by substituting fluorescent labels at the terminus of w-functionalized alkyl chains extending from C-2 of the chroman ring while retaining key binding features of the natural ligand. These compounds were prepared starting from (S)-Trolox® acid VIa esterification, protection, and reduction producing the silyl-protected (S)-Trolox aldehyde that was coupled using Wittig chemistry to different w-hydroxyalkylphosphonium bromides. Reduction of the alkene generated the w-hydroxy functionalized 2-n-alkyl intermediates 9a-d having the necessary 2R stereochemistry. A series of functional group manipulations including mesylation, substitution with azide, and hydride reduction provided w-amino functionalized intermediates 12a-d as well. Coupling intermediates 9a-d and 12a-d with the selected fluorophores (9- anthracene carboxylic acid, 4-chloro-7-nitrobenz-2-oxa-l,3-diazole, 5- dimethylaminonapthalene-l-sulfonyl chloride, and I-methyl-2H-3,1-benzoxazine-2,4(1H)dione), followed by deprotection of the phenolic silyl group, gave the desired fluorescent ligands la-d, 2a-d, 3a-d and 4a-d in good yield. Assessment of their binding affinities with recombinant human a-tocopherol transfer protein (ha-TTP) utilizing fluorescent titration binding assays identified competent ligands for further use in protein studies. Compounds Id (C9-AO-a-Toc) and 2d (C9-NBD-a-Toc) both having nonyl alkyl chain extensions between the chromanol and fluorophore were shown to bind specifically to ha-TTP with dissociation constants (KdS) of approximately 280 nM and 55 nM respectively, as compared to 25 nM for the natural ligand 2R,4'R,^'R-a-tocophQxoL.
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Tesis (Maestría en Enseñanza Superior) UANL
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Tesis (Maestría en Enfermería con Especialidad en Salud Mental y Psiquiatría) UANL
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Tesis (Maestría en Ciencias con Especialidad en Físico-Química) UANL
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Tesis (Maestría en Ciencias con Especialidad en Ingeniería Ambiental) UANL
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Tesis (Maestría en Ciencias de la Ingeniería Mecánica con Especialidad en Materiales) UANL
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Tesis (Maestro en Contaduría Pública) U.A.N.L.
Medidas preventivas para la administración de medicamentos de alto riesgo en servicios ambulatorios.
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Tesis (Maestría en Ciencias de Enfermería) UANL, 2012.
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Tesis (Maestría en Ciencias con Orientación en Matemáticas) UANL, 2012.
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UANL
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UANL
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Tesis (Doctor en Ingeniería de Materiales) U.A.N.L.