Improved Assessment of Ex Vivo Brainstem Neuroanatomy With High-Resolution MRI and DTI at 7 Tesla
Version of Record online: 3 MAY 2011
Copyright © 2011 Wiley-Liss, Inc.
The Anatomical Record
Volume 294, Issue 6, pages 1035–1044, June 2011
How to Cite
Soria, G., De Notaris, M., Tudela, R., Blasco, G., Puig, J., Planas, A. M., Pedraza, S. and Prats-Galino, A. (2011), Improved Assessment of Ex Vivo Brainstem Neuroanatomy With High-Resolution MRI and DTI at 7 Tesla. Anat Rec, 294: 1035–1044. doi: 10.1002/ar.21383
- Issue online: 20 MAY 2011
- Version of Record online: 3 MAY 2011
- Manuscript Accepted: 15 FEB 2011
- Manuscript Received: 27 AUG 2010
- Spanish Government grants by ISCIII, Subdirección General de Evaluación y Fomento de la Investigación. Grant Numbers: PS09/00596, PS09/00527
- diffusion tensor imaging;
- high-resolution MRI;
- 7 Tesla
The aim of the present work was to provide the topography of the main gray nuclei and white matter tracts of the human brainstem at 7 Tesla (7 T) high-field magnetic resonance imaging (MRI) using structural imaging (T1) and diffusion tensor imaging (DTI). Both imaging techniques represent a new field of increasing interest for its potential neuroanatomic and neuropathologic value. Brainstems were obtained postmortem from human donors, fixated by intracarotid perfusion of 10% neutral buffered formalin, and scanned in a Bruker BioSpec 7 T horizontal scanner. 3D-data sets were acquired using the modified driven equilibrium Fourier transform (MDEFT) sequence and Spin Echo-DTI (SE-DTI) sequence was used for DTI acquisition. High-resolution structural MRI and DTI of the human brainstem acquired postmortem reveals its basic cyto- and myeloar-chitectonic organization, only visualized to this moment by histological techniques and higher magnetic field strengths. Brainstem structures that are usually not observed with lower magnetic fields were now topographically identified at midbrain, pons, and medullar levels. The application of high-resolution structural MRI will contribute to precisely determine the extension and topography of brain lesions. Indeed, the current findings will be useful to interpret future high-resolution in vivo MRI studies in living humans. Anat Rec, 2011. © 2011 Wiley-Liss, Inc.