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Disrupted brain metabolic connectivity in a 6-OHDA-induced mouse model of Parkinson’s disease examined using persistent homology-based analysis

Movement impairments in Parkinson’s disease (PD) are caused by the degeneration of dopaminergic neurons and the consequent disruption of connectivity in the cortico-striatal-thalamic loop. This study evaluated brain metabolic connectivity in a 6-Hydroxydopamine (6-OHDA)-induced mouse model of PD usi...

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Autores principales: Im, Hyung-Jun, Hahm, Jarang, Kang, Hyejin, Choi, Hongyoon, Lee, Hyekyoung, Hwang, Do Won, Kim, E. Edmund, Chung, June-Key, Lee, Dong Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030651/
https://www.ncbi.nlm.nih.gov/pubmed/27650055
http://dx.doi.org/10.1038/srep33875
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author Im, Hyung-Jun
Hahm, Jarang
Kang, Hyejin
Choi, Hongyoon
Lee, Hyekyoung
Hwang, Do Won
Kim, E. Edmund
Chung, June-Key
Lee, Dong Soo
author_facet Im, Hyung-Jun
Hahm, Jarang
Kang, Hyejin
Choi, Hongyoon
Lee, Hyekyoung
Hwang, Do Won
Kim, E. Edmund
Chung, June-Key
Lee, Dong Soo
author_sort Im, Hyung-Jun
collection PubMed
description Movement impairments in Parkinson’s disease (PD) are caused by the degeneration of dopaminergic neurons and the consequent disruption of connectivity in the cortico-striatal-thalamic loop. This study evaluated brain metabolic connectivity in a 6-Hydroxydopamine (6-OHDA)-induced mouse model of PD using (18)F-fluorodeoxy glucose positron emission tomography (FDG PET). Fourteen PD-model mice and ten control mice were used for the analysis. Voxel-wise t-tests on FDG PET results yielded no significant regional metabolic differences between the PD and control groups. However, the PD group showed lower correlations between the right caudoputamen and the left caudoputamen and right visual cortex. Further network analyses based on the threshold-free persistent homology framework revealed that brain networks were globally disrupted in the PD group, especially between the right auditory cortex and bilateral cortical structures and the left caudoputamen. In conclusion, regional glucose metabolism of PD was preserved, but the metabolic connectivity of the cortico-striatal-thalamic loop was globally impaired in PD.
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spelling pubmed-50306512016-09-26 Disrupted brain metabolic connectivity in a 6-OHDA-induced mouse model of Parkinson’s disease examined using persistent homology-based analysis Im, Hyung-Jun Hahm, Jarang Kang, Hyejin Choi, Hongyoon Lee, Hyekyoung Hwang, Do Won Kim, E. Edmund Chung, June-Key Lee, Dong Soo Sci Rep Article Movement impairments in Parkinson’s disease (PD) are caused by the degeneration of dopaminergic neurons and the consequent disruption of connectivity in the cortico-striatal-thalamic loop. This study evaluated brain metabolic connectivity in a 6-Hydroxydopamine (6-OHDA)-induced mouse model of PD using (18)F-fluorodeoxy glucose positron emission tomography (FDG PET). Fourteen PD-model mice and ten control mice were used for the analysis. Voxel-wise t-tests on FDG PET results yielded no significant regional metabolic differences between the PD and control groups. However, the PD group showed lower correlations between the right caudoputamen and the left caudoputamen and right visual cortex. Further network analyses based on the threshold-free persistent homology framework revealed that brain networks were globally disrupted in the PD group, especially between the right auditory cortex and bilateral cortical structures and the left caudoputamen. In conclusion, regional glucose metabolism of PD was preserved, but the metabolic connectivity of the cortico-striatal-thalamic loop was globally impaired in PD. Nature Publishing Group 2016-09-21 /pmc/articles/PMC5030651/ /pubmed/27650055 http://dx.doi.org/10.1038/srep33875 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Im, Hyung-Jun
Hahm, Jarang
Kang, Hyejin
Choi, Hongyoon
Lee, Hyekyoung
Hwang, Do Won
Kim, E. Edmund
Chung, June-Key
Lee, Dong Soo
Disrupted brain metabolic connectivity in a 6-OHDA-induced mouse model of Parkinson’s disease examined using persistent homology-based analysis
title Disrupted brain metabolic connectivity in a 6-OHDA-induced mouse model of Parkinson’s disease examined using persistent homology-based analysis
title_full Disrupted brain metabolic connectivity in a 6-OHDA-induced mouse model of Parkinson’s disease examined using persistent homology-based analysis
title_fullStr Disrupted brain metabolic connectivity in a 6-OHDA-induced mouse model of Parkinson’s disease examined using persistent homology-based analysis
title_full_unstemmed Disrupted brain metabolic connectivity in a 6-OHDA-induced mouse model of Parkinson’s disease examined using persistent homology-based analysis
title_short Disrupted brain metabolic connectivity in a 6-OHDA-induced mouse model of Parkinson’s disease examined using persistent homology-based analysis
title_sort disrupted brain metabolic connectivity in a 6-ohda-induced mouse model of parkinson’s disease examined using persistent homology-based analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030651/
https://www.ncbi.nlm.nih.gov/pubmed/27650055
http://dx.doi.org/10.1038/srep33875
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