Academic Thesis

Basic information

Name Inoue Takashi
Belonging department
Occupation name
researchmap researcher code B000003480
researchmap agency Okayama University of Science

Title

VOXEL-BASED MORPHOMETRY OF THE MARMOSET BRAIN: IN VIVO DETECTION OF VOLUME LOSS IN THE SUBSTANTIA NIGRA OF THE MPTP-TREATED PARKINSON'S DISEASE MODEL

Bibliography Type

 

Author

K. Hikishima
K. Ando
Y. Komaki
K. Kawai
R. Yano
T. Inoue
T. Itoh
M. Yamada
S. Momoshima
H. J. Okano
H. Okano

Summary

Movement dysfunction in Parkinson's disease (PD) is caused by the degeneration of dopaminergic (DA) neurons in the substantia nigra (SN). Here, we established a method for voxel-based morphometry (VBM) and automatic tissue segmentation of the marmoset monkey brain using a 7-T animal scanner and applied the method to assess DA degeneration in a PD model, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-treated animals, with tyrosine-hydroxylase staining. The most significant decreases of local tissue volume were detected in the bilateral SN of MPTP-treated marmoset brains (-53.0% in right and -46.5% in left) and corresponded with the location of DA neurodegeneration found in histology (-65.4% in right). In addition to the SN, the decreases were also confirmed in the locus coeruleus, and lateral hypothalamus. VBM using 7-T MRI was effective in detecting volume loss in the SN of the PD-model marmoset. This study provides a potential basis for the application of VBM with ultra-high field MRI in the clinical diagnosis of PD. The developed method may also offer value in automatic whole-brain evaluation of structural changes for the marmoset monkey. (C) 2015 IBRO. Published by Elsevier Ltd. All rights reserved.

Magazine(name)

NEUROSCIENCE

Publisher

PERGAMON-ELSEVIER SCIENCE LTD

Volume

300

Number Of Pages

 

StartingPage

585

EndingPage

592

Date of Issue

2015-08

Referee

Exist

Invited

Not exist

Language

English

Thesis Type

Research papers (academic journals)

ISSN

 

DOI

10.1016/j.neuroscience.2015.05.041

NAID

 

PMID

 

J-GLOBAL ID

 

arXiv ID

 

ORCID Put Code

 

DBLP ID