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When the neuron of a motor unit fires an action potential, it triggers a series of events, leading to a twitch contraction in the muscle fibers. The process of excitation-contraction coupling is crucial in relaying the action potential to the muscle fibers.
The latent period of contraction marks the onset of excitation-contraction coupling, when the action potential propagates across the sarcolemma, preparing the muscle fibers for contraction. As the fibers enter the contraction phase, the...
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Targeting Neuronal Fiber Tracts for Deep Brain Stimulation Therapy Using Interactive, Patient-Specific Models
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Neurovascular coupling during deep brain stimulation.

M Sohail Noor1, Linhui Yu2, Kartikeya Murari3

  • 1Hotchkiss Brain Institute, University of Calgary, Calgary, AB, Canada; Biomedical Engineering, University of Calgary, Calgary, AB, Canada; Department of Electrical and Computer Engineering, University of Calgary, Calgary, AB, Canada; Department of Clinical Neurosciences, University of Calgary, Calgary, AB, Canada.

Brain Stimulation
|April 15, 2020
PubMed
Summary
This summary is machine-generated.

Deep brain stimulation (DBS) effects on brain activity were studied using optical imaging and electrophysiology in rats. High-frequency DBS impacts neurovascular coupling, with corticofugal fiber activation playing a key role.

Keywords:
ElectrophysiologyIntrinsic optical imagingMotor cortexThalamusfMRI

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Area of Science:

  • Neuroscience
  • Biomedical Engineering
  • Medical Imaging

Background:

  • Deep brain stimulation (DBS) is a key treatment for movement disorders, but its precise mechanisms are not fully understood.
  • Functional magnetic resonance imaging (fMRI) is used to study DBS effects, but requires understanding the link between neural and vascular signals.
  • This relationship is poorly characterized at the high frequencies relevant to DBS.

Purpose of the Study:

  • To investigate neurovascular coupling in the rat motor cortex during thalamic DBS.
  • To determine how different DBS frequencies affect neural and vascular responses.
  • To elucidate the contribution of different neural activation pathways to DBS-induced vascular changes.

Main Methods:

  • Simultaneous intrinsic optical imaging and extracellular electrophysiology were used in anesthetized rats.
  • Thalamic DBS was applied at seven different frequencies.
  • Neurovascular coupling was assessed by correlating optical signals (Maximum Change in Reflectance) with electrophysiological measures (Integrated Evoked Potential, multi-unit activity power).
  • Synaptic blockers were used to differentiate between antidromic and orthodromic activation effects.

Main Results:

  • Neurovascular responses (MCR, IEP, MU power) increased linearly up to 60 Hz and then saturated.
  • Blocking orthodromic transmission reduced the optical signal change by approximately 25%.
  • This suggests that activation of corticofugal fibers significantly contributes to thalamic DBS-induced cortical activation.

Conclusions:

  • The vascular response evoked by DBS is linked to both evoked field potentials and multi-unit activity.
  • Understanding neurovascular coupling is crucial for interpreting fMRI studies of DBS.
  • Corticofugal fiber activation is a major factor in the brain's response to thalamic DBS.