Observation of β-ray spectra after penetrating absorbing materials

β-Ray spectra after penetrating absorbing materials of various thicknesses were observed by the use of a scintillation-type β-ray spectrometer equipped with a flat NE-102 plastic scintillator of 5 mm thickness for sources of ⁶⁰Co, ⁹⁰Sr–⁹⁰Y, ¹³⁷Cs, ¹⁴⁷Pm and ²⁰⁴Tl. Although the spectra changed rapidly with increasing absorber thickness, the average β-ray energy was kept nearly constant for a wider range. These results are consistent in that the β-ray absorption curve becomes quasi-linear in a semi-logarithmic plot. Spectra including scattered β-rays from several materials placed behind the source were also measured for ¹³⁷Cs and ²⁰⁴Tl. It may be concluded that mean energy measurements by the use of β-ray spectrometer of this kind is useful for the identification of nuclides in radiation protection purposes even in worse source-conditions.     

Standardization of (18)F using the 4pi(beta+gamma) integral counting technique.

Α 4π(β+γ) integral counting technique using a 4πβ−4πγ detector configuration was adopted for the standardization of ¹⁸F. In this technique, the β-detector is composed of two thin plastic scintillators sandwiching the source, coupled with a slender photomultiplier tube. The β-detector part with the source was inserted into a large well-type NaI(Tl) scintillation detector for γ-ray detection, making a 4πβ−4πγ coincidence counting system. In this work, positron particles were detected with high efficiency in the β-channel and annihilation quanta were also detected with high efficiency in the 4πγ channel. The very small inefficiency of the 4π(β+γ) integral counter for the β-plus branch has been confirmed by EGS5 Monte Carlo simulation. The result using this technique agreed within the uncertainties with the result obtained by the conventional 4πβ−γ coincidence counting with the efficiency extrapolation technique using the same detector configuration and a conventional 4πβ−γ coincidence counter.     

MRI assessment of neuropathology in a transgenic mouse model of Alzheimer's disease.

The cerebral deposition of amyloid beta-peptide, a central event in Alzheimer's disease (AD) pathogenesis, begins several years before the onset of clinical symptoms. Noninvasive detection of AD pathology at this initial stage would facilitate intervention and enhance treatment success. In this study, high-field MRI was used to detect changes in regional brain MR relaxation times in three types of mice: 1). transgenic mice (PS/APP) carrying both mutant genes for amyloid precursor protein (APP) and presenilin (PS), which have high levels and clear accumulation of beta-amyloid in several brain regions, starting from 10 weeks of age; 2). transgenic mice (PS) carrying only a mutant gene for presenilin (PS), which show subtly elevated levels of Abeta-peptide without beta-amyloid deposition; and 3). nontransgenic (NTg) littermates as controls. The transverse relaxation time T(2), an intrinsic MR parameter thought to reflect impaired cell physiology, was significantly reduced in the hippocampus, cingulate, and retrosplenial cortex, but not the corpus callosum, of PS-APP mice compared to NTg. No differences in T(1) values or proton density were detected between any groups of mice. These results indicate that T(2) may be a sensitive marker of abnormalities in this transgenic mouse model of AD.     

beta-Ureidopropionase deficiency: a novel inborn error of metabolism discovered using NMR spectroscopy on urine.

In this work, NMR investigations that led to the discovery of a new inborn error of metabolism, beta-ureidopropionase (UP) deficiency, are reported. 1D (1)H-NMR experiments were performed using a patient's urine. 3-Ureidopropionic acid was observed in elevated concentrations in the urine spectrum. A 1D (1)H-(1)H total correlation spectroscopy (TOCSY) and two heteronuclear 2D NMR techniques (heteronuclear multiple bond correlation (HMBC) and heteronuclear single-quantum correlation (HSQC)) were used to identify the molecular structure of the compound that caused an unknown doublet resonance at 1.13 ppm. Combining the information from the various NMR spectra, this resonance could be assigned to 3-ureidoisobutyric acid. These observations suggested a deficiency of UP. With 1D (1)H-NMR spectroscopy, UP deficiency can be easily diagnosed. The (1)H-NMR spectrum can also be used to diagnose patients suffering from other inborn errors of metabolism in the pyrimidine degradation pathway.     

Further investigations of a simple counting technique for measuring mixtures of two pure beta-emitting radionuclides

A simple liquid scintillation counting technique to measure the activity composition of a mixture containing two known pure β-emitting radionuclides was recently developed at the NMISA. The method has been applied to various two-component mixtures of ³²P, ³³P and ³⁵S, primarily to gauge the effect of spectral energy differences on the method's ability to extract the individual activities. Excellent results were obtained for mixtures of ³³P and ³⁵S, radionuclides with similar, low β energies. Mixtures containing the high-energy β-emitter ³²P were more difficult to resolve, although quenching of the counting sources with CHCl₃ improved mixture resolution.     

Visualization of beta-amyloid plaques in a transgenic mouse model of Alzheimer's disease using MR microscopy without contrast reagents.

The visualization of beta-amyloid plaque deposition in brain, a key feature of Alzheimer's disease (AD), is important for the evaluation of disease progression and the efficacy of therapeutic interventions. In this study, beta-amyloid plaques in the PS/APP transgenic mouse brain, a model of human AD pathology, were detected using MR microscopy without contrast reagents. beta-Amyloid plaques were clearly visible in the cortex, thalamus, and hippocampus of fixed brains of PS/APP mice. The distribution of plaques identified by MRI was in excellent agreement with those found in the immunohistological analysis of the same brain sections. It was also demonstrated that image contrast for beta-amyloid plaques was present in freshly excised nonfixed brains. Furthermore, the detection of beta-amyloid plaques was achieved with a scan time as short as 2 hr, approaching the scan time considered reasonable for in vivo imaging.     

Passive staining: a novel ex vivo MRI protocol to detect amyloid deposits in mouse models of Alzheimer's disease.

Amyloid plaques are one of the hallmarks of Alzheimer's disease (AD). This study evaluated a novel microMRI strategy based on "passive staining" of brain samples by gadoteric acid. The protocol was tested at 4.7 T on control animals and APP/PS1 mice modeling AD lesions. T(1) was strongly decreased in passively stained brains. On high-resolution 3D gradient echo images, the contrast between the cortex and subcortical structures was highly improved due to a T2* effect. The brains of APP/PS1 mice revealed plaques as hypo-intense spots. They appeared larger in long compared to short TE images. This suggests that, after passive staining, plaques caused a susceptibility effect. This easily performed protocol is a complementary method to classic histology to detect the 3D location of plaques. It may also be used for the validation of in vivo MRI protocols for plaque detection by facilitating registration with histology via post mortem MRI.     

MR properties of excised neural tissue following experimentally induced inflammation.

Changes in the MR parameters of inflamed neural tissue were measured in vitro. Tumor necrosis factor-alpha (TNF-alpha) was injected into rat sciatic nerves to induce inflammation with negligible axonal loss and demyelination. The MR parameters, such as T1/T2 relaxation and magnetization transfer (MT), were measured 2 days after TNF-alpha injection and were found to be substantially different from those of normal nerves. The average T1/T2 relaxation times increased, whereas the MT ratio (MTR) and the quantitative MT parameter M0B (which describes the semisolid pool of protons) decreased. The MR parameters correlated very well with the extracellular volume fraction (EM) of neural tissue evaluated by quantitative histopathology. The multicomponent T2 relaxation was shown to provide the best quantitative assessment of changes in neural tissue microstructure, and allowed us to distinguish between the processes of inflammation and demyelination. In comparison, the MT measurements were less successful due to competing contributions of demyelination and pH-sensitive changes in the MT effect.