Magnetic transfer contrast accurately localizes substantia nigra confirmed by histology.

Magnetic transfer contrast accurately localizes substantia nigra confirmed by histology.
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DOI:
10.1016/j.biopsych.2012.07.035
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发表时间:
2013-02-01
影响因子:
10.6
通讯作者:
Lahti AC
Lahti AC
中科院分区:
医学1区
文献类型:
--
作者:
Bolding MS;Reid MA;Avsar KB;Roberts RC;Gamlin PD;Gawne TJ;White DM;den Hollander JA;Lahti AC

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Magnetic Resonance Imaging (MRI) has multiple contrast mechanisms. Like various staining techniques in histology, each contrast type reveals different information about the structure of the brain. However, it is not always clear how structures visible in MRI correspond to structures previously identified by histology. The purpose of this study was to determine if magnetic transfer contrast (MTC) or T2 contrast MRI was better at delineating the substantia nigra. MRI scans were acquired in-vivo from two non-human primates (NHPs). The NHPs were subsequently euthanized, perfused, and their brains sectioned for histological analyses. Each slice was photographed prior to sectioning. Each brain was sectioned into approximately 500, 40-micron sections, encompassing most of the cortex, midbrain, and dorsal parts of the hindbrain. Levels corresponding to anatomical MRI images were selected. From these, adjacent sections were stained using Kluver Barrera (myelin and cell bodies) or tyrosine hydroxylase (TH) (dopaminergic neurons) immunohistochemistry. The resulting images were coregistered to the block-face images using a moving least squares algorithm with similarity transformations. MR images were similarly coregistered to the block-face images, allowing the structures in the MRI to be identified with structures in the histological images. We found that hyperintense (light) areas in MTC images were coextensive with the SN as delineated histologically. The hypointense (dark) areas in T2-weighted images were not coextensive with the SN, but extended partially into the SN and partially into the cerebral peduncles. MTC is a more accurate contrast mechanism than T2-weighting for localizing the SN in vivo.
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