Phase-dependent closed-loop modulation of beta-frequency network oscillations in parkinsonian rats
<p>Normal brain function is associated with an assortment of oscillations of various frequencies, each reflecting the timing of separate computational processes and levels of synchronization within and between brain areas. Stimulation accurately delivered on a specified phase of a given oscill...
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| Other Authors: | |
| Format: | Thesis |
| Language: | English |
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2020
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| _version_ | 1797073108641775616 |
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| author | Rothwell, M |
| author2 | Sharott, A |
| author_facet | Sharott, A Rothwell, M |
| author_sort | Rothwell, M |
| collection | OXFORD |
| description | <p>Normal brain function is associated with an assortment of oscillations of various frequencies, each reflecting the timing of separate computational processes and levels of synchronization within and between brain areas. Stimulation accurately delivered on a specified phase of a given oscillation provides the opportunity to target individual aspects of brain function. To achieve this, we have developed a highly responsive system to produce a continuous online phase-estimate. In addition to stable oscillations, the system accurately tracks the early cycles of short, transient oscillations and can operate across the frequency range of most established neuronal oscillations (4 to 250 Hz).</p>
<p>Here we demonstrate bidirectional modulation of the pathologically elevated parkinsonian beta-band oscillation (around 35 Hz) in 6-OHDA hemi-lesioned rats. Beta phase, monitored using a single channel electrocorticogram above secondary motor cortex, was used to drive electrical stimulation of the globus pallidus or subthalamic nucleus on one of eight phases spanning the oscillation cycle. Stimulation of the early ascending phase suppressed the oscillation whereas stimulation of the early descending phase was amplifying. By implementing a rule that prevented stimulation when the phase estimate was unstable, we achieved a system that could adapt stimulation rate and pattern to respond to the changes produced in the target oscillation. This allowed the electronic system to create and maintain a state of equilibrium with the biological system resulting in continuous stable modulation of the target oscillation over time.</p>
<p>Elevated beta-band activity correlates with motor impairment in humans, primates, and rodents. In an attempt to establish a causal relationship, we used phase-locked stimulation to modulate ongoing cortical beta activity during concurrent assessment of spontaneous forelimb use or goal-directed walking. Despite large deficits in paw use on the injured side during the cylinder task, phase-locked stimulation was unable to modulate forelimb asymmetry. In contrast, consistent reductions in average speed were produced when amplifying beta activity that were driven by a change in running style preference that favoured smaller and slower steps. Altered stand time variance was also observed during individual runs, suggesting that beta-band amplification impaired interlimb coordination. Locomotor deficits were phase-dependent and only present when targeting amplifying phases, thus supporting the functional role of beta-band oscillations in parkinsonian motor impairment.</p>
<p>The results in this study demonstrate the feasibility of phase locked stimulation as a more refined strategy for remediation of pathological beta oscillations in the treatment of the motor symptoms of Parkinson’s disease. Furthermore, they establish the utility of our algorithm and allow for the potential to assess the contribution of rhythmic activity in neuronal computation across a number of brain systems.</p> |
| first_indexed | 2024-03-06T23:17:18Z |
| format | Thesis |
| id | oxford-uuid:678f2b26-076e-47eb-81c8-5b4fdb53d2de |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-06T23:17:18Z |
| publishDate | 2020 |
| record_format | dspace |
| spelling | oxford-uuid:678f2b26-076e-47eb-81c8-5b4fdb53d2de2022-03-26T18:39:07ZPhase-dependent closed-loop modulation of beta-frequency network oscillations in parkinsonian ratsThesishttp://purl.org/coar/resource_type/c_db06uuid:678f2b26-076e-47eb-81c8-5b4fdb53d2deEnglishHyrax Deposit2020Rothwell, MSharott, AMcNamara, C<p>Normal brain function is associated with an assortment of oscillations of various frequencies, each reflecting the timing of separate computational processes and levels of synchronization within and between brain areas. Stimulation accurately delivered on a specified phase of a given oscillation provides the opportunity to target individual aspects of brain function. To achieve this, we have developed a highly responsive system to produce a continuous online phase-estimate. In addition to stable oscillations, the system accurately tracks the early cycles of short, transient oscillations and can operate across the frequency range of most established neuronal oscillations (4 to 250 Hz).</p> <p>Here we demonstrate bidirectional modulation of the pathologically elevated parkinsonian beta-band oscillation (around 35 Hz) in 6-OHDA hemi-lesioned rats. Beta phase, monitored using a single channel electrocorticogram above secondary motor cortex, was used to drive electrical stimulation of the globus pallidus or subthalamic nucleus on one of eight phases spanning the oscillation cycle. Stimulation of the early ascending phase suppressed the oscillation whereas stimulation of the early descending phase was amplifying. By implementing a rule that prevented stimulation when the phase estimate was unstable, we achieved a system that could adapt stimulation rate and pattern to respond to the changes produced in the target oscillation. This allowed the electronic system to create and maintain a state of equilibrium with the biological system resulting in continuous stable modulation of the target oscillation over time.</p> <p>Elevated beta-band activity correlates with motor impairment in humans, primates, and rodents. In an attempt to establish a causal relationship, we used phase-locked stimulation to modulate ongoing cortical beta activity during concurrent assessment of spontaneous forelimb use or goal-directed walking. Despite large deficits in paw use on the injured side during the cylinder task, phase-locked stimulation was unable to modulate forelimb asymmetry. In contrast, consistent reductions in average speed were produced when amplifying beta activity that were driven by a change in running style preference that favoured smaller and slower steps. Altered stand time variance was also observed during individual runs, suggesting that beta-band amplification impaired interlimb coordination. Locomotor deficits were phase-dependent and only present when targeting amplifying phases, thus supporting the functional role of beta-band oscillations in parkinsonian motor impairment.</p> <p>The results in this study demonstrate the feasibility of phase locked stimulation as a more refined strategy for remediation of pathological beta oscillations in the treatment of the motor symptoms of Parkinson’s disease. Furthermore, they establish the utility of our algorithm and allow for the potential to assess the contribution of rhythmic activity in neuronal computation across a number of brain systems.</p> |
| spellingShingle | Rothwell, M Phase-dependent closed-loop modulation of beta-frequency network oscillations in parkinsonian rats |
| title | Phase-dependent closed-loop modulation of beta-frequency network oscillations in parkinsonian rats |
| title_full | Phase-dependent closed-loop modulation of beta-frequency network oscillations in parkinsonian rats |
| title_fullStr | Phase-dependent closed-loop modulation of beta-frequency network oscillations in parkinsonian rats |
| title_full_unstemmed | Phase-dependent closed-loop modulation of beta-frequency network oscillations in parkinsonian rats |
| title_short | Phase-dependent closed-loop modulation of beta-frequency network oscillations in parkinsonian rats |
| title_sort | phase dependent closed loop modulation of beta frequency network oscillations in parkinsonian rats |
| work_keys_str_mv | AT rothwellm phasedependentclosedloopmodulationofbetafrequencynetworkoscillationsinparkinsonianrats |