Altered functional organization of the motor system related to ankle movements in Parkinson’s disease: insights from functional MRI

2011 ◽  
Vol 118 (5) ◽  
pp. 783-793 ◽  
Author(s):  
Petra Katschnig ◽  
Petra Schwingenschuh ◽  
Margit Jehna ◽  
Martin Švehlík ◽  
Katja Petrovic ◽  
...  
2018 ◽  
Vol 129 (8) ◽  
pp. e48-e50
Author(s):  
K.A. Schindlbeck ◽  
A. Vo ◽  
K. Fujita ◽  
P.J. Mattis ◽  
F. Marzinzik ◽  
...  

2020 ◽  
Vol 2 (1) ◽  
Author(s):  
Karsten Mueller ◽  
Dušan Urgošík ◽  
Tommaso Ballarini ◽  
Štefan Holiga ◽  
Harald E Möller ◽  
...  

Abstract Levodopa is the first-line treatment for Parkinson’s disease, although the precise mechanisms mediating its efficacy remain elusive. We aimed to elucidate treatment effects of levodopa on brain activity during the execution of fine movements and to compare them with deep brain stimulation of the subthalamic nuclei. We studied 32 patients with Parkinson’s disease using functional MRI during the execution of finger-tapping task, alternating epochs of movement and rest. The task was performed after withdrawal and administration of a single levodopa dose. A subgroup of patients (n = 18) repeated the experiment after electrode implantation with stimulator on and off. Investigating levodopa treatment, we found a significant interaction between both factors of treatment state (off, on) and experimental task (finger tapping, rest) in bilateral putamen, but not in other motor regions. Specifically, during the off state of levodopa medication, activity in the putamen at rest was higher than during tapping. This represents an aberrant activity pattern probably indicating the derangement of basal ganglia network activity due to the lack of dopaminergic input. Levodopa medication reverted this pattern, so that putaminal activity during finger tapping was higher than during rest, as previously described in healthy controls. Within-group comparison with deep brain stimulation underlines the specificity of our findings with levodopa treatment. Indeed, a significant interaction was observed between treatment approach (levodopa, deep brain stimulation) and treatment state (off, on) in bilateral putamen. Our functional MRI study compared for the first time the differential effects of levodopa treatment and deep brain stimulation on brain motor activity. We showed modulatory effects of levodopa on brain activity of the putamen during finger movement execution, which were not observed with deep brain stimulation.


2016 ◽  
Vol 38 (2) ◽  
pp. 617-630 ◽  
Author(s):  
An Vo ◽  
Wataru Sako ◽  
Koji Fujita ◽  
Shichun Peng ◽  
Paul J. Mattis ◽  
...  

2019 ◽  
Vol 116 (52) ◽  
pp. 26259-26265 ◽  
Author(s):  
Jerrold L. Vitek ◽  
Luke A. Johnson

Parkinson’s disease (PD) is a progressive neurodegenerative movement disorder affecting over 10 million people worldwide. In the 1930s and 1940s there was little understanding regarding what caused PD or how to treat it. In a desperate attempt to improve patients’ lives different regions of the neuraxis were ablated. Morbidity and mortality were common, but some patients’ motor signs improved with lesions involving the basal ganglia or thalamus. With the discovery ofl-dopa the advent of medical therapy began and surgical approaches became less frequent. It soon became apparent, however, that medical therapy was associated with side effects in the form of drug-induced dyskinesia and motor fluctuations and surgical therapies reemerged. Fortunately, during this time studies in monkeys had begun to lay the groundwork to understand the functional organization of the basal ganglia, and with the discovery of the neurotoxin MPTP a monkey model of PD had been developed. Using this model scientists were characterizing the physiological changes that occurred in the basal ganglia in PD and models of basal ganglia function and dysfunction were proposed. This work provided the rationale for the return of pallidotomy, and subsequently deep brain stimulation procedures. In this paper we describe the evolution of these monkey studies, how they provided a greater understanding of the pathophysiology underlying the development of PD and provided the rationale for surgical procedures, the search to understand mechanisms of DBS, and how these studies have been instrumental in understanding PD and advancing the development of surgical therapies for its treatment.


2011 ◽  
Vol 18 (6) ◽  
pp. 807-810 ◽  
Author(s):  
James M. Shine ◽  
Philip B. Ward ◽  
Sharon L. Naismith ◽  
Mark Pearson ◽  
Simon J.G. Lewis

2006 ◽  
Vol 111 (1) ◽  
pp. 104-115 ◽  
Author(s):  
M. Ukmar ◽  
C. Furlan ◽  
R. Moretti ◽  
G. Garbin ◽  
P. Torre ◽  
...  

2004 ◽  
Vol 14 (4) ◽  
pp. 686-690 ◽  
Author(s):  
Bettina Sorger ◽  
Ralf Girnus ◽  
Oliver Schulte ◽  
Barbara Krug ◽  
Klaus Lackner ◽  
...  

2008 ◽  
Vol 23 (S3) ◽  
pp. S548-S559 ◽  
Author(s):  
Jose A. Obeso ◽  
Maria Cruz Rodríguez-Oroz ◽  
Beatriz Benitez-Temino ◽  
Franscisco J. Blesa ◽  
Jorge Guridi ◽  
...  

2011 ◽  
Vol 310 (1-2) ◽  
pp. 79-81 ◽  
Author(s):  
Naroa Ibarretxe-Bilbao ◽  
Carme Junque ◽  
Maria J. Marti ◽  
Eduardo Tolosa

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