Literature DB >> 25740526

Movement-related discharge in the macaque globus pallidus during high-frequency stimulation of the subthalamic nucleus.

Andrew J Zimnik1, Gerald J Nora1, Michel Desmurget2, Robert S Turner3.   

Abstract

Deep brain stimulation (DBS) of the subthalamic nucleus (STN-DBS) has largely replaced ablative therapies for Parkinson's disease. Because of the similar efficacies of the two treatments, it has been proposed that DBS acts by creating an "informational lesion," whereby pathologic neuronal firing patterns are replaced by low-entropy, stimulus-entrained firing patterns. The informational lesion hypothesis, in its current form, states that DBS blocks the transmission of all information from the basal ganglia, including both pathologic firing patterns and normal, task-related modulations in activity. We tested this prediction in two healthy rhesus macaques by recording single-unit spiking activity from the globus pallidus (232 neurons) while the animals completed choice reaction time reaching movements with and without STN-DBS. Despite strong effects of DBS on the activity of most pallidal cells, reach-related modulations in firing rate were equally prevalent in the DBS-on and DBS-off states. This remained true even when the analysis was restricted to cells affected significantly by DBS. In addition, the overall form and timing of perimovement modulations in firing rate were preserved between DBS-on and DBS-off states in the majority of neurons (66%). Active movement and DBS had largely additive effects on the firing rate of most neurons, indicating an orthogonal relationship in which both inputs contribute independently to the overall firing rate of pallidal neurons. These findings suggest that STN-DBS does not act as an indiscriminate informational lesion but rather as a filter that permits task-related modulations in activity while, presumably, eliminating the pathological firing associated with parkinsonism.
Copyright © 2015 the authors 0270-6474/15/353978-12$15.00/0.

Entities:  

Keywords:  basal ganglia; nonhuman primate; reaching

Mesh:

Year:  2015        PMID: 25740526      PMCID: PMC4348192          DOI: 10.1523/JNEUROSCI.4899-14.2015

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  79 in total

1.  Deep brain stimulation creates an informational lesion of the stimulated nucleus.

Authors:  Warren M Grill; Andrea N Snyder; Svjetlana Miocinovic
Journal:  Neuroreport       Date:  2004-05-19       Impact factor: 1.837

2.  Complex locking rather than complete cessation of neuronal activity in the globus pallidus of a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-treated primate in response to pallidal microstimulation.

Authors:  Izhar Bar-Gad; Shlomo Elias; Eilon Vaadia; Hagai Bergman
Journal:  J Neurosci       Date:  2004-08-18       Impact factor: 6.167

3.  Excitotoxic acid lesions of the primate subthalamic nucleus result in transient dyskinesias of the contralateral limbs.

Authors:  I Hamada; M R DeLong
Journal:  J Neurophysiol       Date:  1992-11       Impact factor: 2.714

4.  Functional imaging of sequence learning in Parkinson's disease.

Authors:  Maren Carbon; David Eidelberg
Journal:  J Neurol Sci       Date:  2006-06-05       Impact factor: 3.181

5.  Bilateral deep brain stimulation in Parkinson's disease: a multicentre study with 4 years follow-up.

Authors:  M C Rodriguez-Oroz; J A Obeso; A E Lang; J-L Houeto; P Pollak; S Rehncrona; J Kulisevsky; A Albanese; J Volkmann; M I Hariz; N P Quinn; J D Speelman; J Guridi; I Zamarbide; A Gironell; J Molet; B Pascual-Sedano; B Pidoux; A M Bonnet; Y Agid; J Xie; A-L Benabid; A M Lozano; J Saint-Cyr; L Romito; M F Contarino; M Scerrati; V Fraix; N Van Blercom
Journal:  Brain       Date:  2005-06-23       Impact factor: 13.501

6.  Subthalamic deep brain stimulation increases pallidal firing rate and regularity.

Authors:  René Reese; Arthur Leblois; Frank Steigerwald; Monika Pötter-Nerger; Jan Herzog; H Maximilian Mehdorn; Günther Deuschl; Wassilios G Meissner; Jens Volkmann
Journal:  Exp Neurol       Date:  2011-02-15       Impact factor: 5.330

7.  In a rat model of parkinsonism, lesions of the subthalamic nucleus reverse increases of reaction time but induce a dramatic premature responding deficit.

Authors:  C Baunez; A Nieoullon; M Amalric
Journal:  J Neurosci       Date:  1995-10       Impact factor: 6.167

8.  The primate subthalamic nucleus. III. Changes in motor behavior and neuronal activity in the internal pallidum induced by subthalamic inactivation in the MPTP model of parkinsonism.

Authors:  T Wichmann; H Bergman; M R DeLong
Journal:  J Neurophysiol       Date:  1994-08       Impact factor: 2.714

9.  A common optimization principle for motor execution in healthy subjects and parkinsonian patients.

Authors:  Pierre Baraduc; Stéphane Thobois; Jing Gan; Emmanuel Broussolle; Michel Desmurget
Journal:  J Neurosci       Date:  2013-01-09       Impact factor: 6.167

10.  High-frequency stimulation of the subthalamic nucleus suppresses oscillatory beta activity in patients with Parkinson's disease in parallel with improvement in motor performance.

Authors:  Andrea A Kühn; Florian Kempf; Christof Brücke; Louise Gaynor Doyle; Irene Martinez-Torres; Alek Pogosyan; Thomas Trottenberg; Andreas Kupsch; Gerd-Helge Schneider; Marwan I Hariz; Wim Vandenberghe; Bart Nuttin; Peter Brown
Journal:  J Neurosci       Date:  2008-06-11       Impact factor: 6.167

View more
  15 in total

1.  Dissociable Roles of Pallidal Neuron Subtypes in Regulating Motor Patterns.

Authors:  Qiaoling Cui; Arin Pamukcu; Suraj Cherian; Isaac Y M Chang; Brianna L Berceau; Harry S Xenias; Matthew H Higgs; Shivakumar Rajamanickam; Yi Chen; Xixun Du; Yu Zhang; Hayley McMorrow; Zachary A Abecassis; Simina M Boca; Nicholas J Justice; Charles J Wilson; C Savio Chan
Journal:  J Neurosci       Date:  2021-03-17       Impact factor: 6.167

2.  Information in pallidal neurons increases with parkinsonian severity.

Authors:  Alan D Dorval; Abirami Muralidharan; Alicia L Jensen; Kenneth B Baker; Jerrold L Vitek
Journal:  Parkinsonism Relat Disord       Date:  2015-09-26       Impact factor: 4.891

3.  The human subthalamic nucleus and globus pallidus internus differentially encode reward during action control.

Authors:  Peter Justin Rossi; Corinna Peden; Oscar Castellanos; Kelly D Foote; Aysegul Gunduz; Michael S Okun
Journal:  Hum Brain Mapp       Date:  2017-01-28       Impact factor: 5.038

4.  Long-term labeling of microelectrode tracks with fluorescent latex microspheres.

Authors:  Joshua B Simmons; Robert S Turner; Jonathan C Horton
Journal:  J Neurosci Methods       Date:  2020-07-01       Impact factor: 2.390

5.  Modulation of Neuronal Activity in the Motor Thalamus during GPi-DBS in the MPTP Nonhuman Primate Model of Parkinson's Disease.

Authors:  Abirami Muralidharan; Jianyu Zhang; Debabrata Ghosh; Mathew D Johnson; Kenneth B Baker; Jerrold L Vitek
Journal:  Brain Stimul       Date:  2016-10-11       Impact factor: 8.955

Review 6.  Common therapeutic mechanisms of pallidal deep brain stimulation for hypo- and hyperkinetic movement disorders.

Authors:  Kevin W McCairn; Atsushi Iriki; Masaki Isoda
Journal:  J Neurophysiol       Date:  2015-07-15       Impact factor: 2.714

Review 7.  Deep Brain Stimulation for Movement Disorders of Basal Ganglia Origin: Restoring Function or Functionality?

Authors:  Thomas Wichmann; Mahlon R DeLong
Journal:  Neurotherapeutics       Date:  2016-04       Impact factor: 7.620

Review 8.  Deep Brain Stimulation: Expanding Applications.

Authors:  Anand Tekriwal; Gordon Baltuch
Journal:  Neurol Med Chir (Tokyo)       Date:  2015-10-15       Impact factor: 1.742

Review 9.  Deep brain stimulation: current challenges and future directions.

Authors:  Andres M Lozano; Nir Lipsman; Hagai Bergman; Peter Brown; Stephan Chabardes; Jin Woo Chang; Keith Matthews; Cameron C McIntyre; Thomas E Schlaepfer; Michael Schulder; Yasin Temel; Jens Volkmann; Joachim K Krauss
Journal:  Nat Rev Neurol       Date:  2019-03       Impact factor: 42.937

10.  Neural activity during a simple reaching task in macaques is counter to gating and rebound in basal ganglia-thalamic communication.

Authors:  Bettina C Schwab; Daisuke Kase; Andrew Zimnik; Robert Rosenbaum; Marcello G Codianni; Jonathan E Rubin; Robert S Turner
Journal:  PLoS Biol       Date:  2020-10-13       Impact factor: 9.593

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.