Considerable evidence suggests a close relationship between vascular and degenerative pathology in the human hippocampus. Due to the intrinsic fragility of its vascular network, the hippocampus appears less able to cope with hypoperfusion and anoxia than other cortical areas. Although hippocampal blood supply is generally provided by the collateral branches of the posterior cerebral artery (PCA) and the anterior choroidal artery (AChA), different vascularization patterns have been detected postmortem. To date, a methodology that enables the classification of individual hippocampal vascularization patterns in vivo has not been established. In this study, using high-resolution 7 Tesla time-of-flight angiography data (0.3 mm isotropic resolution) in young adults, we classified individual variability in hippocampal vascularization patterns involved in medial temporal lobe blood supply in vivo. A strong concordance between our classification and previous autopsy findings was found, along with interesting anatomical observations, such as the variable contribution of the AChA to hippocampal supply, the relationships between hippocampal and PCA patterns, and the different distribution patterns of the right and left hemispheres. The approach presented here for determining hippocampal vascularization patterns in vivo may provide new insights into not only the vulnerability of the hippocampus to vascular and neurodegenerative diseases but also hippocampal vascular plasticity after exercise training.
Germination, the process whereby a dry, quiescent seed springs to life, has been a focus of plant biologist for many years, yet the early events following water uptake, during which metabolism of the embryo is restarted, remain enigmatic. Here, the nature of the cues required for this restarting in oilseed rape (Brassica napus) seed has been investigated. A holistic in vivo approach was designed to display the link between the entry and allocation of water, metabolic events and structural changes occurring during germination. For this, we combined functional magnetic resonance imaging with Fourier transform infrared microscopy, fluorescence-based respiration mapping, computer-aided seed modeling and biochemical tools. We uncovered an endospermal lipid gap, which channels water to the radicle tip, from whence it is distributed via embryonic vasculature toward cotyledon tissues. The resumption of respiration is initiated first in the endosperm, only later spreading to the embryo. Sugar metabolism and lipid utilization are linked to the spatiotemporal sequence of tissue rehydration. Together, this imaging study provides insights into the spatial aspects of key events in oilseed rape seeds leading to germination. It demonstrates how seed architecture predetermines the pattern of water intake, which sets the stage for the orchestrated restart of life.
Computational fluid dynamic (CFD) simulations of blood flow provide new insights into the hemodynamics of vascular pathologies such as cerebral aneurysms. Understanding the relations between hemodynamics and aneurysm initiation, progression, and risk of rupture is crucial in diagnosis and treatment. Recent studies link the existence of vortices in the blood flow pattern to aneurysm rupture and report observations of embedded vortices -a larger vortex encloses a smaller one flowing in the opposite direction -whose implications are unclear. We present a clustering-based approach for the visual analysis of vortical flow in simulated cerebral aneurysm hemodynamics. We show how embedded vortices develop at saddle-node bifurcations on vortex core lines and convey the participating flow at full manifestation of the vortex by a fast and smart grouping of streamlines and the visualization of group representatives. The grouping result may be refined based on spectral clustering generating a more detailed visualization of the flow pattern, especially further off the core lines. We aim at supporting CFD engineers researching the biological implications of embedded vortices.
Epidemiological population studies impose information about a set of subjects (a cohort) to characterize disease-specific risk factors. Cohort studies comprise heterogenous variables describing the medical condition as well as demographic and lifestyle factors and, more recently, medical image data. We propose an Interactive Visual Analysis (IVA) approach that enables epidemiologists to rapidly investigate the entire data pool for hypothesis validation and generation. We incorporate image data, which involves shape-based object detection and the derivation of attributes describing the object shape. The concurrent investigation of image-based and non-image data is realized in a web-based multiple coordinated view system, comprising standard views from information visualization and epidemiological data representations such as pivot tables. The views are equipped with brushing facilities and augmented by 3D shape renderings of the segmented objects, e.g., each bar in a histogram is overlaid with a mean shape of the associated subgroup of the cohort. We integrate an overview visualization, clustering of variables and object shape for data-driven subgroup definition and statistical key figures for measuring the association between variables. We demonstrate the IVA approach by validating and generating hypotheses related to lower back pain as part of a qualitative evaluation.
Here, we present an extension to our previously published structural ultrahigh resolution T1-weighted magnetic resonance imaging (MRI) dataset with an isotropic resolution of 250 µm, consisting of multiple additional ultrahigh resolution contrasts. Included are up to 150 µm Time-of-Flight angiography, an updated 250 µm structural T1-weighted reconstruction, 330 µm quantitative susceptibility mapping, up to 450 µm structural T2-weighted imaging, 700 µm T1-weighted back-to-back scans, 800 µm diffusion tensor imaging, one hour continuous resting-state functional MRI with an isotropic spatial resolution of 1.8 mm as well as more than 120 other structural T1-weighted volumes together with multiple corresponding proton density weighted acquisitions collected over ten years. All data are from the same participant and were acquired on the same 7 T scanner. The repository contains the unprocessed data as well as (pre-)processing results. The data were acquired in multiple studies with individual goals. This is a unique and comprehensive collection comprising a “human phantom” dataset. Therefore, we compiled, processed, and structured the data, making them publicly available for further investigation.
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