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1.
Med Intensiva ; 37(1): 6-11, 2013.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-22749460

RESUMO

AIM: A study is made of the influence of alcohol and/or drug abuse upon traumatismo recurrence, with an analysis of the influence of such abuse upon the time to appearance of first injury in patients without antecedents of trauma. DESIGN: A prospective observational study was made. SETTING: Trauma patients admitted to the Intensive care Unit (ICU) of a University Hospital. PATIENTS: Trauma patients admitted to the ICU. INTERVENTION: None. MAIN MEASUREMENTS: Trauma recurrence was defined by a history of previous trauma requiring medical care. The presence of alcohol and other drugs of abuse were determined upon admission after severe trauma. RESULTS: Out of the 166 trauma patients admitted to the ICU during the study period, 102 (87 males) were included in the study. Some substance was detected in 51 patients (50%), most frequently in the males (48/87, p<0.02). The most frequently detected substance was alcohol (39%), followed by cannabis (12%) and cocaine (7%), while more than one substance was found in 10 patients (9.8%). Of the 102 patients, 42 were recurrent trauma cases, and 32 (76%) of them were substance-positive, while only 10 were substance-negative (p<0.001). Of the 60 patients without antecedents of trauma, 19 (32%) were substance-positive, and these were significantly younger (34.3±9 years) than the 41 subjects who were substance-negative (48±23 years) (p<0.001). CONCLUSION: Alcohol and/or drug abuse increases the likelihood of recurrent trauma and may shorten the mean trauma-free period among patients without a history of trauma by almost 15 years.


Assuntos
Alcoolismo/complicações , Transtornos Relacionados ao Uso de Substâncias/complicações , Ferimentos e Lesões/etiologia , Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Recidiva , Fatores de Tempo
2.
Phys Rev E ; 106(5-2): 055205, 2022 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-36559494

RESUMO

The collisionless ion-Weibel instability is a leading candidate mechanism for the formation of collisionless shocks in many astrophysical systems, where the typical distance between particle collisions is much larger than the system size. Multiple laboratory experiments aimed at studying this process utilize laser-driven (I≳10^{15} W/cm^{2}), counterstreaming plasma flows (V≲2000 km/s) to create conditions unstable to Weibel-filamentation and growth. This technique intrinsically produces temporally varying plasma conditions at the midplane of the interaction where Weibel-driven B fields are generated and studied. Experiments discussed herein demonstrate robust formation of Weibel-driven B fields under multiple plasma conditions using CH, Al, and Cu plasmas. Linear theory based on benchmarked radiation-hydrodynamic FLASH calculations is compared with Fourier analyses of proton images taken ∼5-6 linear growth times into the evolution. The new analyses presented here indicate that the low-density, high-velocity plasma-conditions present during the first linear-growth time (∼300-500 ps) sets the spectral characteristics of Weibel filaments during the entire evolution. It is shown that the dominant wavelength (∼300µm) at saturation persists well into the nonlinear phase, consistent with theory under these experimental conditions. However, estimates of B-field strength, while difficult to determine accurately due to the path-integrated nature of proton imaging, are shown to be in the ∼10-30 T range, an order of magnitude above the expected saturation limit in homogenous plamas but consistent with enhanced B fields in the midplane due to temporally varying plasma conditions in experiments.

3.
Rev Sci Instrum ; 87(7): 073301, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27475550

RESUMO

Radiochromic films (RCF) are commonly used in dosimetry for a wide range of radiation sources (electrons, protons, and photons) for medical, industrial, and scientific applications. They are multi-layered, which includes plastic substrate layers and sensitive layers that incorporate a radiation-sensitive dye. Quantitative dose can be retrieved by digitizing the film, provided that a prior calibration exists. Here, to calibrate the newly developed EBT3 and HDv2 RCFs from Gafchromic™, we used the Stanford Medical LINAC to deposit in the films various doses of 10 MeV photons, and by scanning the films using three independent EPSON Precision 2450 scanners, three independent EPSON V750 scanners, and two independent EPSON 11000XL scanners. The films were scanned in separate RGB channels, as well as in black and white, and film orientation was varied. We found that the green channel of the RGB scan and the grayscale channel are in fact quite consistent over the different models of the scanner, although this comes at the cost of a reduction in sensitivity (by a factor ∼2.5 compared to the red channel). To allow any user to extend the absolute calibration reported here to any other scanner, we furthermore provide a calibration curve of the EPSON 2450 scanner based on absolutely calibrated, commercially available, optical density filters.


Assuntos
Dosimetria Fotográfica/instrumentação , Dosimetria Fotográfica/métodos , Modelos Teóricos , Calibragem , Dosimetria Fotográfica/normas
4.
J Atten Disord ; 14(1): 86-94, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-19805621

RESUMO

OBJECTIVE: The article discusses a feasibility study conducted to examine whether Pay Attention!, an intervention training sustained, selective, alternating, and divided attention, could be utilized in a clinical setting with children diagnosed with ADHD, and whether children who received the intervention made attention and executive functioning gains. METHOD: After a diagnostic and baseline evaluation, 23 school-aged children with ADHD participate in up to 16 sessions of Pay Attention! and the outcomes are evaluated. RESULTS: Results show the intervention is feasible to administer and acceptable to participants. Parents and clinicians rate fewer ADHD symptoms following the intervention and report improvements in executive function. Child performance on neuropsychological tests showed improvements in fluid reasoning and cognitive flexibility and working memory. CONCLUSION: The findings suggest that a randomized clinical trial of Pay Attention! is warranted to investigate its viability as a treatment for attention and executive functioning deficits in ADHD.


Assuntos
Transtorno do Deficit de Atenção com Hiperatividade/terapia , Terapia Comportamental , Função Executiva , Adolescente , Atenção , Criança , Feminino , Humanos , Masculino , Testes Neuropsicológicos , Seleção de Pacientes , Resultado do Tratamento
5.
Cytobios ; 82(329): 81-99, 1995.
Artigo em Inglês | MEDLINE | ID: mdl-7587376

RESUMO

Several novel intermediate filament-associated proteins (IFAPs) have been discovered using hybridoma technology on multiple sclerosis plaque tissue. One of these, designated the G.3.5 antigen, is a desmin-binding IFAP in skeletal and cardiac muscle. It has been suggested that because of sequence similarities to alpha-actinin the G.3.5 antigen is an alpha-actinin-like protein which may cross-link actin and intermediate filaments in the cytoskeleton. In this study, it is reported that (1) the G.3.5 antigen is present in hepatocytes in addition to the previously described astrocytes, skeletal and cardiac myocytes, fibroblasts, and several other non-nervous tissues; (2) in myocytes and hepatocytes, the G.3.5 and alpha-actinins do not co-localize; (3) by transmission electron microscopy the G.3.5 antigen appears to be a rod-shaped dimer similar to alpha-actinin; (4) isolation of the G.3.5 antigen does not simultaneously isolate alpha-actinin; and (5) limited proteolysis of the G.3.5 antigen and alpha-actinin generates dissimilar maps. In binding studies, alpha-actinin cross-links actin but has no effect on desmin; the G.3.5 antigen does not appear to cross-link actin, desmin or mixtures of both under the assay conditions. These results support the hypothesis that the G.3.5 antigen is a novel IFAP related to alpha-actinin, but do not support a role for the antigen as a cross-linker between intermediate filaments and actin.


Assuntos
Actinina , Proteínas de Filamentos Intermediários , Fígado/metabolismo , Músculo Esquelético/metabolismo , Actinina/análise , Actinina/metabolismo , Actinina/ultraestrutura , Sequência de Aminoácidos , Animais , Proteínas de Filamentos Intermediários/análise , Proteínas de Filamentos Intermediários/metabolismo , Proteínas de Filamentos Intermediários/ultraestrutura , Dados de Sequência Molecular , Ratos
6.
Am J Obstet Gynecol ; 182(2): 296-9, 2000 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-10694327

RESUMO

OBJECTIVE: We sought to compare the effects of fluoxetine, imipramine, and nortriptyline on spontaneous and serotonin-activated contractile activity of the uterine rings from midterm and term pregnant rats. STUDY DESIGN: Uterine rings from timed-pregnant Sprague-Dawley rats on day 14 (midgestation) and day 22 (term gestation) were used for isometric tension recording. Responses to cumulative concentrations of fluoxetine, imipramine, nortriptyline, and serotonin in the absence and presence of the monoamine reuptake inhibitors were studied. RESULTS: Neither of the monoamine reuptake inhibitors significantly influenced spontaneous contractile activity, whereas the concentration-dependent increase in activity induced by serotonin was inhibited in rings from both midterm and term pregnant rats. CONCLUSIONS: The reported increase in preterm delivery in women receiving fluoxetine during the third trimester cannot be explained by a direct effect on uterine contractility.


Assuntos
Fluoxetina/farmacologia , Inibidores Seletivos de Recaptação de Serotonina/farmacologia , Serotonina/farmacologia , Contração Uterina/efeitos dos fármacos , Útero/fisiologia , Inibidores da Captação Adrenérgica/farmacologia , Animais , Antidepressivos Tricíclicos/farmacologia , Relação Dose-Resposta a Droga , Feminino , Imipramina/farmacologia , Contração Isométrica/efeitos dos fármacos , Contração Isométrica/fisiologia , Nortriptilina/farmacologia , Gravidez , Ratos , Ratos Sprague-Dawley , Contração Uterina/fisiologia , Útero/efeitos dos fármacos
7.
Cytobios ; 94(375): 39-61, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-9853368

RESUMO

The G.3.5 antigen (named for the monoclonal antibody which recognizes it) has been characterized as an intermediate filament-associated protein found in a variety of tissue types, including human and rat astrocytes, rat skeletal and cardiac myocytes, fibroblasts, rat hepatocytes, and chicken and fish retinal tissues. Sequencing of proteolytic fragments indicated a high degree of similarity to alpha-actinin. Comparison of the G.3.5 antigen to alpha-actinin revealed that alpha-actinin and the G.3.5 antigen migrated similarly in reducing and non-reducing environments and had similar molecular masses (approximately 100,000). Overlay-immunoblotting assays indicated that the G.3.5 antigen and alpha-actinin could bind filamentous actin and desmin simultaneously. In contrast, immunocytochemistry indicated the G.3.5 antigen and alpha-actinin were immunologically distinct in tissue sections. The results of this study suggest that the G.3.5 antigen is an isoform of alpha-actinin which may serve to cross-link intermediate filaments to microfilaments, and that other isoforms of alpha-actinin may also share this property.


Assuntos
Citoesqueleto de Actina/metabolismo , Actinina/metabolismo , Proteínas de Filamentos Intermediários/metabolismo , Filamentos Intermediários/metabolismo , Proteínas Musculares/metabolismo , Isoformas de Proteínas/metabolismo , Citoesqueleto de Actina/ultraestrutura , Actinina/química , Actinina/imunologia , Actinina/isolamento & purificação , Sequência de Aminoácidos , Animais , Anticorpos Monoclonais/imunologia , Especificidade de Anticorpos , Bovinos , Galinhas , Humanos , Hibridização In Situ , Filamentos Intermediários/ultraestrutura , Dados de Sequência Molecular , Peso Molecular , Proteínas Musculares/química , Proteínas Musculares/imunologia , Músculo Esquelético/química , Músculo Liso/química , Isoformas de Proteínas/química , Isoformas de Proteínas/imunologia , Ratos , Homologia de Sequência de Aminoácidos
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