152 resultados para Substructure
Resumo:
In the central nervous system, iron in several proteins is involved in many important processes: oxygen transportation, oxidative phosphorylation, mitochondrial respiration, myelin production, the synthesis and metabolism of neurotransmitters. Abnormal iron homoeostasis can induce cellular damage through hydroxyl radical production, which can cause the oxidation, modification of lipids, proteins, carbohydrates, and DNA, lead to neurotoxicity. Moreover increased levels of iron are harmful and iron accumulations are typical hallmarks of brain ageing and several neurodegenerative disorders particularly PD. Numerous studies on post mortem tissue report on an increased amount of total iron in the substantia nigra in patients with PD also supported by large body of in vivo findings from Magnetic Resonance Imaging (MRI) studies. The importance and approaches for in vivo brain iron assessment using multiparametric MRI is increased over last years. Quantitative MRI may provide useful biomarkers for brain integrity assessment in iron-related neurodegeneration. Particularly, a prominent change in iron- sensitive T2* MRI contrast within the sub areas of the SN overlapping with nigrosome 1 were shown to be a hallmark of Parkinson's Disease with high diagnostic accuracy. Moreover, differential diagnosis between Parkinson's Disease (PD) and atypical parkinsonian syndromes (APS) remains challenging, mainly in the early phases of the disease. Advanced brain MR imaging enables to detect the pathological changes of nigral and extranigral structures at the onset of clinical manifestations and during the course of the disease. The Nigrosome-1 (N1) is a substructure of the healthy Substantia Nigra pars compacta enriched by dopaminergic neurons; their loss in Parkinson’s disease and atypical parkinsonian syndromes is related to the iron accumulation. N1 changes are supportive MR biomarkers for diagnosis of these neurodegenerative disorders, but its detection is hard with conventional sequences, also using high field (3T) scanner. Quantitative susceptibility mapping (QSM), an iron-sensitive technique, enables the direct detection of Neurodegeneration
Resumo:
Gravitational lensing is a powerful tool to investigate the properties of the distribution of matter, be it barionic or dark. In this work we take advantage of Strong Gravitational Lensing to infer the properties of one of the galaxy-scale substructures that makes up the cluster MACSJ1206. It is relatively easy to model the morphology of the visible components of a galaxy, while the morphology of the dark matter distribution cannot be so easily constrained. Being sensitive to the whole mass, strong lensing provides a way to probe DM distribution, and this is the reason why it is the best tool to study the substructure. The goal of this work consists of performing an analysis of the substructure previously mentioned, an early type galaxy (ETG), by analyzing the highly magnified Einstein ring around it, in order to put stringent constraints on its matter distribution, that, for an ETG, is commonly well described by an isothermal profilele. This turns out to be interesting for three main different reasons. It is well known that galaxies in clusters are subject to interaction processes, both dynamic and hydrodynamic, that can significantly modify the distribution of matter within them. Therefore, finding a different profile from the one usually expected could be a sign that the galaxy has undergone processes that have changed its structure. Studying the mass distribution also means studying the dark matter component, which not only still presents great questions today, but which is also not obviously distributed in the same way as in an isolated galaxy. What emerges from the analysis is that the total mass distribution of the galaxy under examination turns out to have a slope much steeper than the isothermal usually expected.
