21 research outputs found
Characterization of Large Volume 3.5 x 8 inches LaBr3:Ce Detectors
The properties of large volume cylindrical 3.5 x 8 inches (89 mm x 203 mm)
LaBr3:Ce scintillation detectors coupled to the Hamamatsu R10233-100SEL
photo-multiplier tube were investigated. These crystals are among the largest
ones ever produced and still need to be fully characterized to determine how
these detectors can be utilized and in which applications. We tested the
detectors using monochromatic gamma-ray sources and in-beam reactions producing
gamma rays up to 22.6 MeV; we acquired PMT signal pulses and calculated
detector energy resolution and response linearity as a function of gamma-ray
energy. Two different voltage dividers were coupled to the Hamamatsu
R10233-100SEL PMT: the Hamamatsu E1198-26, based on straightforward resistive
network design, and the LABRVD, specifically designed for our large volume
LaBr3:Ce scintillation detectors, which also includes active semiconductor
devices. Because of the extremely high light yield of LaBr3:Ce crystals we
observed that, depending on the choice of PMT, voltage divider and applied
voltage, some significant deviation from the ideally proportional response of
the detector and some pulse shape deformation appear. In addition, crystal
non-homogeneities and PMT gain drifts affect the (measured) energy resolution
especially in case of high-energy gamma rays. We also measured the time
resolution of detectors with different sizes (from 1x1 inches up to 3.5x8
inches), correlating the results with both the intrinsic properties of PMTs and
GEANT simulations of the scintillation light collection process. The detector
absolute full energy efficiency was measured and simulated up to gamma-rays of
30 Me
Characterization of Large Volume 3.5″ x 8″ LaBr3:Ce Detectors for the HECTOR+ array
A selection of the properties of large volume, cylindrical 3.5" x 8" LaBr 3 :Ce scintillation detectors coupled to a 3.5" PMT (model R10233-1000SEL from HAMAMATSU) and a special designed Voltage Divider (LABRVD) will be discussed. A number of 10 of such detectors constitute the HECTOR + array which, in fall 2012, measured at GSI coupled to the AGATA DEMOSTRATOR at the PRESPEC experimental setup. These crystals are among the largest ever produced and needed to be characterized. We have performed several tests and here we discuss, in particular, the energy resolution measured using monochromatic γ −ray sources and in-beam reactions producing γ −rays up to 22.6 MeV. As already measured in two previous works a saturation in the energy resolution was observed in case of high energy gamma rays. Crystal non-homogeneities and PMT gain drifts can affect the resolution of measurements especially in case of high energy γ −rays
Endogenous proteolytic activity in a rat model of spontaneous cerebral stroke
We evaluated the expression of two extra-cellular protease systems in a model of spontaneous cerebrovascular pathology: spontaneously hypertensive stroke-prone rats (SHRSP). The appearance of brain damage in individual animals was imaged and followed by means of magnetic resonance imaging (MRI). In situ zymography of brain slices obtained 3 days after the appearance of brain damage showed an increase in plasminogen activator (PA)/plasmin activity that co-localised with the cerebral damage detected by MRI; there was also concomitant accumulation/activation of inflammatory cells in the damaged area. Proteolytic activity was inhibited by the urokinase-specific inhibitor amiloride but not by an antibody against tissue-type plasminogen activator (t-PA). SDS-PAGE zymography of brain extracts revealed the presence of 58 kDa plasminogen-dependent lysis areas in the ischemic and non-ischemic tissues, and a 33 kDa lysis area in ischemic tissue only. An antibody against t-PA inhibited the former, whereas the latter was inhibited by amiloride. The specific induction of urokinase-type plasminogen activator (u-PA) in the damaged tissue was further confirmed by the fact that both u-PA protein mass and mRNA were markedly increased in the damaged cerebral areas. Concomitant metalloproteinase-2 (MMP-2) activation was only observed in the damaged area. These data suggest that u-PA is expressed and selectively catalyses proteolysis in the injured area of spontaneous brain damage in SHRSP
Treatment with statins after induction of focal ischemia in rats reduces the extent of brain damage
OBJECTIVE:
In the present study, MRI has been used to investigate therapeutic intervention with statins in a model of permanent focal cerebral ischemia in rat.
METHODS AND RESULTS:
Brain ischemia was induced in rats by the permanent occlusion of middle cerebral artery (MCAO) and the brain infarct size followed up in alive animals 2, 24, and 48 hours after MCAO, using the trace of apparent diffusion coefficient [Tr(D)] maps and T2-weighted images. In vehicle-treated rats, the infarct volumes increased by 38.5% and 89% after 24 and 48 hours, respectively, compared with the damage detected at 2 hours after MCAO. Treatment with simvastatin (20 mg/kg) after MCAO prevented the increase in brain infarct volume occurring at 24 hours and induced a 46.6% reduction after 48 hours. This effect was similar to that observed when simvastatin was administered before the induction of focal ischemia. T2W-MRI images confirmed these findings. The neuroprotective effects of simvastatin were paralleled by an increase in endothelial NO synthase immunoreactivity, detectable in the brain of simvastatin-treated rats.
CONCLUSIONS:
Statins, in addition to their preventive effect on cerebral ischemia, exert a neuroprotective role in the attenuation of brain damage after acute stroke
Treatment with statins after induction of focal ischemia in rats reduces the extent of brain damage
Objective-In the present study, MRI has been used to investigate therapeutic intervention with statins in a model of permanent focal cerebral ischemia in rat.
Methods and Results-Brain ischemia was induced in rats by the permanent occlusion of middle cerebral artery (MCAO) and the brain infarct size followed up in alive animals 2, 24, and 48 hours after MCAO, using the trace of apparent diffusion coefficient [Tr(D)] maps and T2-weighted images. In vehicle-treated rats, the infarct volumes increased by 38.5% and 89% after 24 and 48 hours, respectively, compared with the damage detected at 2 hours after MCAO. Treatment with simvastatin (20 mg/kg) after MCAO prevented the increase in brain infarct volume occurring at 24 hours and induced a 46.6% reduction after 48 hours. This effect was similar to that observed when simvastatin was administered before the induction of focal ischemia. T2W-MRI images confirmed these findings. The neuroprotective effects of simvastatin were paralleled by an increase in endothelial NO synthase immunoreactivity, detectable in the brain of simvastatin-treated rats.
Conclusions-Statins, in addition to their preventive effect on cerebral ischemia, exert a neuroprotective role in the attenuation of brain damage after acute stroke
A new approach for assessing winning and losing plant species facing climate change on the GLORIA alpine summits
Climate change in alpine habitats has a direct impact on vascular plant species, and is leading to changes in species abundance and distribution. Alpine plant communities are expected to experience a turnover of species over time, due to the loss of cold-adapted specialists and the upslope migration of more thermophilic taxa. Therefore, assessments of single species changes are important for research and conservation. Here, we propose a new analysis protocol for the GLORIA (GLobal Observation Research Initiative in Alpine environments) network, and potentially, for other monitoring programmes capable of defining winning and losing plant species. The proposed approach involves the non-parametric Cliff's 'Delta' measure of 'effect size', which provides a measure of the intensity of species abundance changes over time and is applicable for vegetation data collected using both re-visitation and long-term monitoring approaches. Compared to other methods, Cliff's 'Delta' was more conservative and efficient in detecting winning/losing taxa, as well as being suitable to analyse data of rare species with few records. To test the effectivity of the Cliff 'Delta' method, we analysed the vegetation data from three Italian GLORIA sites. We investigated 413 vascular plant species and found a total of 41 winning and 24 losing species. Moreover, we used Cliff 'Delta' to assess whether plant assemblages are responding differently among sites and plant growth forms. Our findings showed that alpine plant communities are changing faster on Apennines sites and that growth form types respond differently across the study sites