199 research outputs found
Perfil de desempenho de técnicas coproscópicas Coproplus® e Hoffman, Pons e Janner no diagnóstico de giardíase
Justificativa e Objetivos: Os parasitas intestinais representam um problema de saúde pública
no Brasil, e sua identificação é feita rotineiramente, por meio de várias técnicas diagnósticas.
Muitas dessas técnicas são criticadas por suas limitações, como a de Hoffman, Pons e Janner.
Considerou-se avaliar o grau de sensibilidade diagnóstica dessa técnica em comparação ao
método coproscópico de coleta e filtragem Coproplus®, uma vez que esta metodologia também
é baseada na concentração de estruturas parasíticas e é uma adaptação prática aos métodos
usuais, pois não há documentos diagnósticos de protozoários. Métodos: A análise gráfica pelo
método de Bland-Altman mostrou que há concordância entre os dois métodos de identificação
dos cistos avaliados, ao traçar as diferenças entre o número de cistos contra as médias de ambos
os valores. Resultados: Verificou-se que, para os protozoários, o uso de apenas um método
parasitológico de Hoffman, Pons e Janner não é suficiente para identificar todas as amostras.
Conclusão: Os métodos têm se mostrado eficazes na identificação de parasitas intestinais, mas
nem todos os agentes foram identificados simultaneamente em ambas as técnicas e números de
cistos, o que leva à conclusão de que uma técnica pode complementar a outra
The background in the neutrinoless double beta decay experiment GERDA
The GERmanium Detector Array (GERDA) experiment at the Gran Sasso underground
laboratory (LNGS) of INFN is searching for neutrinoless double beta decay of
76Ge. The signature of the signal is a monoenergetic peak at 2039 keV, the
Q-value of the decay, Q_bb. To avoid bias in the signal search, the present
analysis does not consider all those events, that fall in a 40 keV wide region
centered around Q_bb. The main parameters needed for the neutrinoless double
beta decay analysis are described. A background model was developed to describe
the observed energy spectrum. The model contains several contributions, that
are expected on the basis of material screening or that are established by the
observation of characteristic structures in the energy spectrum. The model
predicts a flat energy spectrum for the blinding window around Q_bb with a
background index ranging from 17.6 to 23.8*10^{-3} counts/(keV kg yr). A part
of the data not considered before has been used to test if the predictions of
the background model are consistent. The observed number of events in this
energy region is consistent with the background model. The background at Q-bb
is dominated by close sources, mainly due to 42K, 214Bi, 228Th, 60Co and alpha
emitting isotopes from the 226Ra decay chain. The individual fractions depend
on the assumed locations of the contaminants. It is shown, that after removal
of the known gamma peaks, the energy spectrum can be fitted in an energy range
of 200 kev around Q_bb with a constant background. This gives a background
index consistent with the full model and uncertainties of the same size
Simulation of Special Bubble Detectors for PICASSO
The PICASSO project is a cold dark matter (CDM) search experiment relying on
the superheated droplet technique. The detectors use superheated freon liquid
droplets (active material) dispersed and trapped in a polymerized gel. This
detection technique is based on the phase transition of superheated droplets at
about room temperature and ambient pressure. The phase transition is induced by
nuclear recoils when an atomic nucleus in the droplets interacts with incoming
subatomic particles. This includes CDM particles candidate as the neutralino (a
yet-to-discover particle predicted in extensions of the Standard Model of
particle physics). Simulations performed to understand the detector response to
neutrons and alpha particles are presented along with corresponding data
obtained at the Montreal Laboratory.Comment: 13 pages, 4 figures. To appear in the Proceedings of the 14th
International Conference on Solid State Dosimetry, June 27 - July 2 2004,
Yale University, New Haven, CT, US
Grey and white matter correlates of recent and remote autobiographical memory retrieval:Insights from the dementias
The capacity to remember self-referential past events relies on the integrity of a distributed neural network. Controversy exists, however, regarding the involvement of specific brain structures for the retrieval of recently experienced versus more distant events. Here, we explored how characteristic patterns of atrophy in neurodegenerative disorders differentially disrupt remote versus recent autobiographical memory. Eleven behavioural-variant frontotemporal dementia, 10 semantic dementia, 15 Alzheimer's disease patients and 14 healthy older Controls completed the Autobiographical Interview. All patient groups displayed significant remote memory impairments relative to Controls. Similarly, recent period retrieval was significantly compromised in behavioural-variant frontotemporal dementia and Alzheimer's disease, yet semantic dementia patients scored in line with Controls. Voxel-based morphometry and diffusion tensor imaging analyses, for all participants combined, were conducted to investigate grey and white matter correlates of remote and recent autobiographical memory retrieval. Neural correlates common to both recent and remote time periods were identified, including the hippocampus, medial prefrontal, and frontopolar cortices, and the forceps minor and left hippocampal portion of the cingulum bundle. Regions exclusively implicated in each time period were also identified. The integrity of the anterior temporal cortices was related to the retrieval of remote memories, whereas the posterior cingulate cortex emerged as a structure significantly associated with recent autobiographical memory retrieval. This study represents the first investigation of the grey and white matter correlates of remote and recent autobiographical memory retrieval in neurodegenerative disorders. Our findings demonstrate the importance of core brain structures, including the medial prefrontal cortex and hippocampus, irrespective of time period, and point towards the contribution of discrete regions in mediating successful retrieval of distant versus recently experienced events
Strong Gravitational Lensing as a Probe of Gravity, Dark-Matter and Super-Massive Black Holes
Whereas considerable effort has been afforded in understanding the properties
of galaxies, a full physical picture, connecting their baryonic and dark-matter
content, super-massive black holes, and (metric) theories of gravity, is still
ill-defined. Strong gravitational lensing furnishes a powerful method to probe
gravity in the central regions of galaxies. It can (1) provide a unique
detection-channel of dark-matter substructure beyond the local galaxy group,
(2) constrain dark-matter physics, complementary to direct-detection
experiments, as well as metric theories of gravity, (3) probe central
super-massive black holes, and (4) provide crucial insight into galaxy
formation processes from the dark matter point of view, independently of the
nature and state of dark matter. To seriously address the above questions, a
considerable increase in the number of strong gravitational-lens systems is
required. In the timeframe 2010-2020, a staged approach with radio (e.g. EVLA,
e-MERLIN, LOFAR, SKA phase-I) and optical (e.g. LSST and JDEM) instruments can
provide 10^(2-4) new lenses, and up to 10^(4-6) new lens systems from
SKA/LSST/JDEM all-sky surveys around ~2020. Follow-up imaging of (radio) lenses
is necessary with moderate ground/space-based optical-IR telescopes and with
30-50m telescopes for spectroscopy (e.g. TMT, GMT, ELT). To answer these
fundamental questions through strong gravitational lensing, a strong investment
in large radio and optical-IR facilities is therefore critical in the coming
decade. In particular, only large-scale radio lens surveys (e.g. with SKA)
provide the large numbers of high-resolution and high-fidelity images of lenses
needed for SMBH and flux-ratio anomaly studies.Comment: White paper submitted to the 2010 Astronomy & Astrophysics Decadal
Surve
Grafted Human Embryonic Progenitors Expressing Neurogenin-2 Stimulate Axonal Sprouting and Improve Motor Recovery after Severe Spinal Cord Injury
7 p.Background: Spinal cord injury (SCI) is a widely spread pathology with currently no effective treatment for any symptom. Regenerative medicine through cell transplantation is a very attractive strategy and may be used in different non-exclusive ways to promote functional recovery. We investigated functional and structural outcomes after grafting human embryonic neural progenitors (hENPs) in spinal cord-lesioned rats.Methods and Principal Findings: With the objective of translation to clinics we have chosen a paradigm of delayed grafting, i.e., one week after lesion, in a severe model of spinal cord compression in adult rats. hENPs were either naive or engineered to express Neurogenin 2 (Ngn2). Moreover, we have compared integrating and non-integrating lentiviral vectors, since the latter present reduced risks of insertional mutagenesis. We show that transplantation of hENPs transduced to express Ngn2 fully restore weight support and improve functional motor recovery after severe spinal cord compression at thoracic level. This was correlated with partial restoration of serotonin innervations at lumbar level, and translocation of 5HT1A receptors to the plasma membrane of motoneurons. Since hENPs were not detectable 4 weeks after grafting, transitory expression of Ngn2 appears sufficient to achieve motor recovery and to permit axonal regeneration. Importantly, we also demonstrate that transplantation of naive hENPs is detrimental to functional recovery.Conclusions and Significance: Transplantation and short-term survival of Ngn2-expressing hENPs restore weight support after SCI and partially restore serotonin fibers density and 5HT1A receptor pattern caudal to the lesion. Moreover, grafting of naive-hENPs was found to worsen the outcome versus injured only animals, thus pointing to the possible detrimental effect of stem cell-based therapy per se in SCI. This is of major importance given the increasing number of clinical trials involving cell grafting developed for SCI patients.This study was supported by the European Union FP6 "RESCUE" STREP; the "Institut pour la Recherche sur la Moelle Epiniere"; the "Academie de Medecine"; the "Societe Francaise de Neurochirurgie"; "Verticale" and the "Association Demain Debout Aquitaine". The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript
Protoplasmic Astrocytes Enhance the Ability of Neural Stem Cells to Differentiate into Neurons In Vitro
Protoplasmic astrocytes have been reported to exhibit neuroprotective effects on neurons, but there has been no direct evidence for a functional relationship between protoplasmic astrocytes and neural stem cells (NSCs). In this study, we examined neuronal differentiation of NSCs induced by protoplasmic astrocytes in a co-culture model. Protoplasmic astrocytes were isolated from new-born and NSCs from the E13-15 cortex of rats respectively. The differentiated cells labeled with neuron-specific marker β-tubulin III, were dramatically increased at 7 days in the co-culture condition. Blocking the effects of brain-derived neurotrophic factor (BDNF) with an anti-BDNF antibody reduced the number of neurons differentiated from NSCs when co-cultured with protoplasmic astrocytes. In fact, the content of BDNF in the supernatant obtained from protoplasmic astrocytes and NSCs co-culture media was significantly greater than that from control media conditions. These results indicate that protoplasmic astrocytes promote neuronal differentiation of NSCs, which is driven, at least in part, by BDNF
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