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2.
Rev. Soc. Cardiol. Estado de Säo Paulo ; 33(supl. 2B): 170-170, abr. 2023. tab
Article de Portugais | CONASS, Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-1438058

RÉSUMÉ

INTRODUÇÃO: Em 5% a 6% dos IAM não são observadas lesões obstrutivas maiores que 50%, sendo estes classificados como MINOCA (Infarto do Miocárdio com Artérias Coronárias não Obstrutivas). Estudos maiores de longo prazo demonstraram que o prognóstico desses pacientes não é benigno com risco aumentado de morte e novos eventos cardiovasculares. MÉTODOS: Nesta coorte de centro único, todos os pacientes que preencheram os critérios diagnósticos para MINOCA com (1) IAM (2) ausência de estenose coronária ≥ 50% na artéria relacionada ao infarto e (3) nenhuma outra causa específica clinicamente evidente entre março de 2000 e junho de 2022 foram incluídos com um acompanhamento médio de 30 (9,5-67,3) meses. As características da amostra foram descritas em frequências e valores medianos (p25%-p75%). A incidência de um novo evento cardiovascular (CV) em 36 meses após a MINOCA foi estimada pelo método de Kaplan-Meier e o teste de log-rank aplicado para comparar os grupos, acompanhado de intervalos de confiança de 95% e alfa de 5% (R 3,6,1 para MacOS). RESULTADOS: Dos 126 pacientes, 57,1% eram mulheres com cerca de 50 anos de idade (42,0-57,8). 20,6% tinham diabetes, 47,6% dislipidemia, 60,3% hipertensão e 20% IAM prévio. A apresentação clínica predominante foi IAMSSST (55,6%) e 7 pacientes tiveram um episódio de morte súbita abortada durante a internação. 38,1% dos pacientes não tiveram uma etiologia identificada. O mecanismo fisiopatológico mais prevalente foi ruptura da placa < 50% (16,7%), seguido de tromboembolismo (13,5%) e dissecção espontânea de coronária (13,5%). Apenas 3,2% realizaram tomografia de coerência óptica (OCT) ou ultrassom intravascular (IVUS). Nenhum teste provocativo foi realizado. 44,4% realizaram ressonância magnética cardíaca (RMC), com mediana de tempo para realização de 180,0 (60,0-707,5) dias após o evento. Em relação à medicação prescrita na alta hospitalar, 79,4% tiveram betabloqueador e IECA/BRA prescritos, 14,3% iniciaram anticoagulação e apenas 34,1% receberam dupla antiagregação plaquetária (DAP). A incidência do desfecho composto (morte CV, novo IAM, AVC e internação CV) em 36 meses foi de 15% (IC95% 8,9%-24,6%). A incidência de novo IAM foi de 6,3% (N=8), de AVC 2,4% (N=3), de hospitalização CV 17,5% (N=22) e apenas um óbito. CONCLUSÃO: Chama a atenção o risco do desfecho primário em 36 meses. Notavelmente, a maior parte da incidência foi atribuída à hospitalização CV. Um número importante de pacientes recebeu alta sem etiologia conhecida para sua apresentação clínica e, consequentemente, sem tratamento individualizado.

3.
Med. infant ; 19(3): 199-201, sept. 2012.
Article de Espagnol | LILACS | ID: lil-774337

RÉSUMÉ

La infección respiratoria es un importante motivo de internación en pediatría. Ultimamente se identificó a los Metapneumovirus como agentes etiológicos de infecciones respiratorias. Se estudiaron 897 niños internados a los cuales se les realizó el estudio de detección de virus respiratorios, incluyendo Metapneumovirus, por inmunofluorescencia indirecta entre noviembre y diciembre de 2009. Se detectaron 55 pacientes con muestras positivas para virus respiratorios en secreciones nasofaringeas: 33 de ellas fueron positivas para Metapneumovirus. Se analizaron las características epidemiológicas, clínicas y evolutivas de niños con Metapneumovirus en forma retrospectiva. La edad media fue de 45 meses (r =0 a 204) y el 60% eran mayores de un año. Diecisiete de los mayores de un año (85%) presentaron comorbilidades. La bronquiolitis fue la forma clínica más frecuente en los menores de un año [9 (69%) y 8 (61%)] requirieron oxígeno. Todos tuvieron buena evolución. Conclusiones: Metapneumovirus fue causa de internación en los menores de un año y en los mayores con enfermedad de base. La presentación clínica fue similar a la producida por otros virus. Se observó su predominio sobre otros virus como causa de infección respiratoria entre noviembre y diciembre de 2009.


Respiratory infection is a common cause for hospital admission in children. Recently, the metapneumovirus has been identified as a causative agent of respiratory infection. Between Novem-ber and December 2009, 897 pediatric inpatients were studied for respiratory viruses, including the metapneumovirus, using indirect immunofluorescence techniques. Of all patients, 55 had positive nasopharyngeal samples for respiratory viruses; 33 were positive for the metapneumovirus. The epidemio-logical and clinical features and outcome of the children with metapneumovirus were retrospectively analyzed. Mean age was 45 months (r = 0 to 204) and 60% was older than one year. Seventeen of the children older than one year (85%) presented with comorbidities. Bronchiolitis was the most com-mon clinical presentation in children younger than one year. Nine (69%) and eight (61%) children, respectively, required oxygen therapy. Outcome was good in all patients. Conclu-sions: Metapneumovirus was the cause of hospital admission in children under one year of age and in children older than one year with an underlying disease. Symptoms were similar to those produced by other viruses. Between November and December 2009, the metapneumovirus was more commonly observed than other viruses as a cause of respiratory infection.


Sujet(s)
Humains , Mâle , Femelle , Nouveau-né , Nourrisson , Enfant d'âge préscolaire , Hôpitaux pédiatriques , Hôpitaux publics , Infections de l'appareil respiratoire/diagnostic , Infections de l'appareil respiratoire/étiologie , Metapneumovirus , Argentine , Bronchiolite/étiologie
4.
Gene Expr Patterns ; 10(4-5): 207-13, 2010 Jun.
Article de Anglais | MEDLINE | ID: mdl-20302971

RÉSUMÉ

Vitronectin (vn) is a cell-adhesive glycoprotein present in blood and extracellular matrix of all vertebrates. In the present study we reported the cDNA cloning of Xenopus laevisvitronectin and its spatial and temporal expression pattern during the embryonic development of this important model organism. The deduced amino acid sequence of Xenopus laevis vn showed 49%, 47% and 43% identity with human, chicken and zebrafish orthologs, respectively, whereas the comparison with Xenopus tropicalis vn presented 85% identity. The structural organization consisting of a somatomedin B domain and two hemopexin-like domains was similar to higher vertebrate vitronectins. The vn transcripts were detected from stage 28 onward. At tadpole stages, vn is expressed in heart, gut derivatives and in the notochord. The protein was detected in heart, liver, foregut, pronephros and notochord at stages 43 and 47 of Xenopus embryos. Our results suggest that vitronectin is developmentally regulated and could participate in embryo organogenesis.


Sujet(s)
Vitronectine/métabolisme , Xenopus laevis/métabolisme , Séquence d'acides aminés , Animaux , ADN complémentaire , Électrophorèse sur gel de polyacrylamide , Développement embryonnaire , Hybridation in situ , Microscopie de fluorescence , Données de séquences moléculaires , RT-PCR , Similitude de séquences d'acides aminés , Vitronectine/composition chimique , Xenopus laevis/embryologie
5.
Zygote ; 15(3): 273-83, 2007 Aug.
Article de Anglais | MEDLINE | ID: mdl-17637109

RÉSUMÉ

In this work we carried out ultrastructural, autoradiographic and biochemical analyses of the follicular epithelium during C. cranwelli previtellogenesis. This study revealed that the follicular epithelium in early previtellogenesis is constituted of a single layer of squamous homogeneous cells. During mid-previtellogenesis two types of cells develop: dark cells and clear cells. The follicular dark cells are actively involved in the synthesis of RNA, which is transferred to the oocyte through the interface. In late previtellogenesis the dark cells show apoptotic characteristics such as chromatin condensation, DNA fragmentation and cytoplasm shrinkage. This process forms apoptotic bodies that seem to be engulfed by the oocyte. Our results show evidence that, during mid- and late C. cranwelli previtellogenesis, the follicular epithelium undergoes remodelling processes interacting with the oocyte.


Sujet(s)
Ovocytes/ultrastructure , Follicule ovarique/ultrastructure , Vitellogenèse , Animaux , Anura , Épithélium/ultrastructure , Femelle , Microscopie électronique à transmission
6.
Zygote ; 15(2): 149-57, 2007 May.
Article de Anglais | MEDLINE | ID: mdl-17462107

RÉSUMÉ

The aim of the present study was to investigate the physiological role and the expression pattern of heterologous gap junctions during Xenopus laevis vitellogenesis. Dye transfer experiments showed that there are functional gap junctions at the oocyte/follicle cell interface during the vitellogenic process and that octanol uncouples this intercellular communication. The incubation of vitellogenic oocytes in the presence of biotinylated bovine serum albumin (b-BSA) or fluorescein dextran (FDX), showed that oocytes develop stratum of newly formed yolk platelets. In octanol-treated follicles no sign of nascent yolk sphere formation was observed. Thus, experiments in which gap junctions were downregulated with octanol showed that coupled gap junctions are required for endocytic activity. RT-PCR analysis showed that the expression of connexin 43 (Cx43) was first evident at stage II of oogenesis and increased during the subsequent vitellogenic stages (III, IV and V), which would indicate that this Cx is related to the process that regulates yolk uptake. No expression changes were detected for Cx31 and Cx38 during vitellogenesis. Based on our results, we propose that direct gap junctional communication is a requirement for endocytic activity, as without the appropriate signal from surrounding epithelial cells X. laevis oocytes were unable to endocytose VTG.


Sujet(s)
Jonctions communicantes/physiologie , Vitellogenèse/physiologie , Vitellogénines/pharmacologie , Animaux , Bovins , Communication cellulaire , Connexine 43/métabolisme , Connexines/métabolisme , Jaune d'œuf/métabolisme , Endocytose , Cellules épithéliales/métabolisme , Femelle , Techniques immunoenzymatiques , Octanols/pharmacologie , Ovocytes/cytologie , Ovocytes/physiologie , Ovogenèse/physiologie , Follicule ovarique/cytologie , Follicule ovarique/physiologie , ARN messager/génétique , ARN messager/métabolisme , RT-PCR , Xenopus laevis
7.
Plant Dis ; 84(5): 595, 2000 May.
Article de Anglais | MEDLINE | ID: mdl-30841368

RÉSUMÉ

Colletotrichum gloeosporioides was isolated from symptomatic strawberry (Fragaria × ananassa Duch. 'Chandler') growing in Lules (Tucumán, Argentina). Isolates were characterized based on several criteria. Potato dextrose agar (PDA) was used to evaluate cultural and morphological characteristics of the isolates. After 10 days on PDA at 28°C under continuous white light, colonies showed abundant aerial, cottony white to pale beige growth, with orange asexual fruiting bodies in older colonies. Isolates displayed cylindrical conidia, rounded at both ends, averaging 10.4 × 3.9 µm (length by width). A sexual phase (perithecia) was observed in all isolates in 2-month-old cultures on PDA at 28°C under continuous white light. Pathogenicity tests were conducted with healthy plants of cvs. Pájaro and Chandler. Spray inoculation with conidial suspensions (106 conidia per ml) resulted in disease symptoms (petiole and crown lesions with wilting of crown-infected plants) 7 days after inoculation. Infection progressed at a higher rate in Pájaro than in Chandler. Reisolations from infected strawberry lesions yielded isolates with characteristics identical to the isolate used to inoculate the host. Based on morphological and cultural characteristics, isolates were identified as C. gloeosporioides Penz. & Sacc. (teleomorph Glomerella cingulata Spauld & H. Schenk) (1). This is the first report of C. gloeosporioides causing strawberry anthracnose in northwestern Argentina. Reference: (1) P. S. Gunnell and W. D. Gubler. Mycol. 84:157, 1992.

8.
Curr Microbiol ; 31(6): 327-31, 1995 Dec.
Article de Anglais | MEDLINE | ID: mdl-8528003

RÉSUMÉ

The temperature-sensitive cell division cycle (cdc) G1 mutants cdc28 and cdc35 show decreased mitochondrial volumes with respect to the wild type strain A364A (WT) at the restrictive temperature. Of the three criteria of mitochondrial biogenesis studied, that is, number of mitochondria per cell, relative area of the cell occupied by mitochondria, or relative area of mitochondria occupied by inner membranes, only the second indicator was significantly lower in cdc mutants than in the WT. The mitochondrial inner membranes development did not compensate for the decrease in the organelles volume. Apparently, the reduced mitochondrial biogenesis was not due to the temperature shift because the relative area of the cell occupied by mitochondria was already significantly lower at 25 degrees C in cdc mutants. The specific fluxes of oxygen consumption confirmed that the respiratory capacity of cdc mutants is largely impaired in respect to the WT. Cdc28 and cdc35 mutants of Saccharomyces cerevisiae had been previously shown to exhibit high respiratory quotients (from 3 to 7) in respect to the WT (RQ approximately 1.0), which correlated with carbon and energy uncoupling probably the result of glucose-induced catabolite repression [Aon MA, Mónaco ME, Cortassa S (1995) Exp Cell Res 217, 42-51; Mónaco ME, Valdecantos PA, Aon MA (1995) Exp Cell Res 217, 52-56].


Sujet(s)
Gènes cdc/génétique , Mitochondries/métabolisme , Saccharomyces cerevisiae/cytologie , Phase G1 , Cinétique , Mitochondries/ultrastructure , Mutation , Consommation d'oxygène , Saccharomyces cerevisiae/génétique , Saccharomyces cerevisiae/métabolisme , Température
9.
Exp Cell Res ; 217(1): 42-51, 1995 Mar.
Article de Anglais | MEDLINE | ID: mdl-7867719

RÉSUMÉ

Cell proliferation arrest at 37 degrees C (restrictive temperature) of the cell division cycle (cdc) mutants of Saccharomyces cerevisiae cdc28, cdc35, cdc19, cdc21, and cdc17 was correlated with carbon and energy uncoupling. At 37 degrees C, cdc mutants diverted to biomass synthesis only 3 to 4% and 8 to 24% of the fluxes of carbon consumed and ATP obtained by catabolism, respectively, compared with 48 and 34% in the wild-type strain A364A. At the permissive temperature (25 degrees C), the wild type showed similar carbon and energy coupling indexes as at 37 degrees C. However, carbon and energy coupling indexes were two- to sevenfold higher at 25 degrees than at 37 degrees C in cdc mutants; e.g., at 25 degrees C two- to sevenfold higher amounts of carbon and ATP were directed to biomass production than at 37 degrees C. The wild-type strain exhibited a purely oxidative glucose catabolism at 37 degrees C (RQ approximately 1.0), while the cell proliferation arrest of cdc mutants at the same temperature was characterized by fermentative metabolism. At 37 degrees C, cdc mutants directed 50 to 60% of the carbon to ethanol production; 3 to 12% of the carbon was recovered as glycerol in cdc mutants as well as in the wild type. The proliferation arrest of the cell division cycle mutant cdc28 correlated with a significant decrease in the incorporation of radioactive precursors into DNA, RNA, and proteins. In the presence of 8-hydroxyquinoline, the wild-type strain underwent cell proliferation arrest and also exhibited metabolic uncoupling with bioenergetic and catabolic behavior similar to that of the cdc mutants at 37 degrees C. Experimental evidence obtained with cdc19, whose defective gene product is pyruvate kinase, suggests that the primary defect of cdc mutants correlates with a metabolically, highly uncoupled yeast cell. The results presented point to the existence of strong carbon and energy uncoupling together with cell division arrest exhibited by cdc mutants at the restrictive temperature. The degree of uncoupling appears to be tuned, at least in part, by the increase in flux of sugar catabolism through the ethanol fermentative pathway.


Sujet(s)
Cycle cellulaire/physiologie , Saccharomyces cerevisiae/cytologie , Carbone/métabolisme , Cycle cellulaire/génétique , Protéines du cycle cellulaire/génétique , Division cellulaire/physiologie , Métabolisme énergétique/physiologie , Éthanol/métabolisme , Fermentation , Structures macromoléculaires , Mutation , Hydroxy-8 quinoléine/pharmacologie , Phénotype , Saccharomyces cerevisiae/génétique , Saccharomyces cerevisiae/métabolisme , Température
10.
Exp Cell Res ; 217(1): 52-6, 1995 Mar.
Article de Anglais | MEDLINE | ID: mdl-7867720

RÉSUMÉ

Several cell division cycle (cdc) mutants of Saccharomyces cerevisiae (cdc28, cdc35, cdc19, cdc21, and cdc17) at the restrictive temperature (37 degrees C) in the presence of 1% glucose and defined medium divert most of the carbon (approximately 50%) to ethanol production with low biomass growth yields (Yglc) that correlate with carbon and energy uncoupling and arrest of cell proliferation. The cdc mutants studied are shown to be glucose-repressed, while this was not the case for the wild-type A364A (WT). At 37 degrees C, in the presence of 1% glycerol, derepressed cdc28 mutant cells did not show arrest of cell division and carbon and energy uncoupling since the Yglc levels measured were similar to those of the WT strain. These results suggest that the increased fermentative ability and carbon and energy uncoupling exhibited in the presence of glucose by cdc mutants with respect to those exhibited by the WT may be due to catabolite repression.


Sujet(s)
Cycle cellulaire/physiologie , Glucose/pharmacologie , Saccharomyces cerevisiae/cytologie , Carbone/métabolisme , Cycle cellulaire/génétique , Protéines du cycle cellulaire/génétique , Division cellulaire/effets des médicaments et des substances chimiques , Division cellulaire/physiologie , Métabolisme énergétique/physiologie , Mutation , Saccharomyces cerevisiae/effets des médicaments et des substances chimiques , Saccharomyces cerevisiae/génétique , Saccharomyces cerevisiae/métabolisme
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