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Uszynski, I.

Publications and source records attributed to Uszynski, I..

2 recordsLinked to original sources

In vivo mapping of the deep and superficial whitematter connectivity in the chimpanzee brain

Mapping the chimpanzee brain connectome, and comparing it to humans, is key to our understanding of similarities and differences in primate evolution that occurred after the split from their common ancestor around 6 million years ago. In contrast with macaque species brain studies, less studies have specifically addressed the structural connectivity of the chim-panzee brain and its comparison with the human brain. Most comparative studies in the liter-ature focus on the anatomy of the cortex and deep nuclei to evaluate how their morphometry and asymmetry differs from that of the human brain, and some studies have emerged concern-ing the study of brain connectivity between primates. In this work, we established a new white matter atlas of the deep and superficial white matter structural connectivity in chimpanzees. In vivo anatomical and diffusion weighted magnetic resonance imaging (MRI) data were collected on a 3 Tesla magnetic resonance imaging (MRI) system in 39 chimpanzees. These datasets were subsequently processed using a dedicated fiber clustering pipeline adapted to the chimpanzee brain enabling us to create two novel deep and superficial white matter connectivity atlases representative of the chimpanzee brain. These atlases provide the scientific community with an important and novel set of reference data for understanding the commonalities and differ-ences of the structural connectivity between the human and chimpanzee brains, which will contribute to a better understanding of the hominin brain evolution.

neuroscience↗

Characterization of early white matter changes in CADASIL using microscopic diffusion imaging and relaxometry

Background and purposeCerebral small vessel diseases (SVDs) are characterized by early white matter (WM) changes, whose pathological underpinnings are yet poorly understood. CADASIL is a monogenic and archetypal SVD, providing an ideal model for investigating these changes. Here, we used multicompartment microscopic diffusion imaging and relaxometry to elucidate microstructural changes underlying early WM abnormalities in CADASIL. MethodsWe acquired diffusion MRI data with a multiple-shell Q-space sampling strategy, and relaxometry T1 and T2 data, with a 160 and 80-m isotropic resolution respectively, ex vivo, in CADASIL and control mice. Diffusion datasets were computed with the Neurite Orientation Dispersion and Density Imaging model to extract the neurite density index, the extracellular free water and the orientation dispersion index. Relaxometry datasets were computed with a 3-compartment myelin water imaging model to extract the myelin content. MRI metrics were compared between CADASIL and control mice using voxel and WM tract-based analyses and with electron microscopy analysis. ResultsWM in CADASIL mice displayed a widespread reduction in general fractional anisotropy, a large increase in extracellular free water, a reduction in the myelin content, but no reduction in neurite density. Electron microscopy analysis showed a {bsim}2-fold increase in the extracellular spaces and an elevation of the g-ratio indicative of myelin sheath thinning in CADASIL WM. ConclusionOur findings suggest that accumulation of interstitial fluid and myelin damage are 2 major factors underlying early WM changes in CADASIL. Advanced diffusion MRI and relaxometry are promising approaches to decipher the underpinnings of WM alterations in SVDs.

neuroscience↗