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@ARTICLE{Apetz:863492,
author = {Apetz, Nadine and Kordys, Elena and Simon, Mascha and Mang,
Britta and Aswendt, Markus and Wiedermann, Dirk and
Neumaier, Bernd and Drzezga, Alexander and Timmermann, Lars
and Endepols, Heike},
title = {{E}ffects of subthalamic deep brain stimulation on striatal
metabolic connectivity in a rat hemiparkinsonian model},
journal = {Disease models $\&$ mechanisms},
volume = {12},
number = {5},
issn = {1754-8411},
address = {Cambridge},
publisher = {Company of Biologists Limited},
reportid = {FZJ-2019-03546},
pages = {dmm039065 -},
year = {2019},
abstract = {Deep brain stimulation (DBS) in the subthalamic nucleus
(STN) has been successfully used for the treatment of
advanced Parkinson’s disease, although the underlying
mechanisms are complex and not well understood. There are
conflicting results about the effects of STN-DBS on neuronal
activity of the striatum, and its impact on functional
striatal connectivity is entirely unknown. We therefore
investigated how STN-DBS changes cerebral metabolic activity
in general and striatal connectivity in particular. We used
ipsilesional STN stimulation in a hemiparkinsonian rat model
in combination with [18F]FDOPA-PET, [18F]FDG-PET and
metabolic connectivity analysis. STN-DBS reversed
ipsilesional hypometabolism and contralesional
hypermetabolism in hemiparkinsonian rats by increasing
metabolic activity in the ipsilesional ventrolateral
striatum and by decreasing it in the contralesional
hippocampus and brainstem. Other STN-DBS effects were
subject to the magnitude of dopaminergic lesion severity
measured with [18F]FDOPA-PET, e.g. activation of the
infralimbic cortex was negatively correlated to lesion
severity. Connectivity analysis revealed that, in healthy
control animals, left and right striatum formed a bilateral
functional unit connected by shared cortical afferents,
which was less pronounced in hemiparkinsonian rats. The
healthy striatum was metabolically connected to the
ipsilesional substantia nigra in hemiparkinsonian rats only
(OFF condition). STN-DBS (ON condition) established a new
functional striatal network, in which interhemispheric
striatal connectivity was strengthened, and both the
dopamine-depleted and the healthy striatum were functionally
connected to the healthy substantia nigra. We conclude that
both unilateral dopamine depletion and STN-DBS affect the
whole brain and alter complex interhemispheric networks.},
cin = {INM-5 / INM-2},
ddc = {570},
cid = {I:(DE-Juel1)INM-5-20090406 / I:(DE-Juel1)INM-2-20090406},
pnm = {572 - (Dys-)function and Plasticity (POF3-572)},
pid = {G:(DE-HGF)POF3-572},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:31064773},
UT = {WOS:000470069500010},
doi = {10.1242/dmm.039065},
url = {https://juser.fz-juelich.de/record/863492},
}