Neuroprosthetics - PowerPoint PPT Presentation

1 / 20
About This Presentation
Title:

Neuroprosthetics

Description:

Retina ganglion or bipolar cells. Cochlea/Ear spiral ganglion cells. Motor prostheses nerve-muscle junction ... In each example interface between ... – PowerPoint PPT presentation

Number of Views:118
Avg rating:3.0/5.0
Slides: 21
Provided by: bdh
Category:

less

Transcript and Presenter's Notes

Title: Neuroprosthetics


1
Neuroprosthetics
  • Week 4
  • Neuron Modelling

2
Implants excite neurons
  • Retina ganglion or bipolar cells
  • Cochlea/Ear spiral ganglion cells
  • Motor prostheses nerve-muscle junction
  • In each example interface between electrode and
    neuronal membrane

3
Passive properties of neuronal membrane
  • Resistance from intra and extra cellular fluids
  • Capacitance of membrane (like a cable)
  • Combination means spatial and temporal filtering
    of voltage signals
  • Typical low pass RC circuit losses/fidelity
  • Spinal motor neurons or axons from retina
    ganglion to thalamus in brain must reliably carry
    signals with a frequency up to 4KHz/1KHz for up
    to 1 metre

4
Passive limitations
  • Rise and fall of signals given by
  • V(t) V(0)exp(-t/T) where T RC
  • Typical RC 1 to 100msec so voltage changes
    are slowed
  • Same equation for distance that a signal can be
    detected
  • V(x) V(0)exp(-x/X) where X length constant
  • Typical X is a few hundred micrometers

5
Passive response
  • Voltage profile for a constant current on
    peripheral nerve of KW

6
Active Membranes
  • Active membranes overcome temporal and spatial
    degradations
  • Ionic gradients exist between the inside and
    outside of cells
  • Exchanges between sodium, calcium and potassium
    ions driven in and out of cells
  • Action potential brief, transient, regenerating
    depolarization
  • Resting potential typically -70mV. External
    stimulus brings membrane to threshold. Cell fires
    or not, peak amplitude may reach 40mV

7
Ion channels
  • Whole cell currents represent the ensemble of
    thousands of individual channels
  • Thousands of individual ion channels are
    responsible for membrane conductance changes
  • Channels are selective for different types of
    ions

8
Gating
  • Time dependence of the opening and closing of a
    channel
  • Probability of finding a channel in an open or
    closed state as a function of
  • membrane potential
  • the presence of a drug or neurotransmitter

9
Permeation
  • Conductive properties of a channel in terms of
    its selectivity for specific ions
  • The rate at which ions can pass through the
    channel (hence max current)
  • Effects of blocking drugs

10
Permeation
  • Conductive properties of a channel in terms of
    its selectivity for specific ions
  • The rate at which ions can pass through the
    channel (hence max current)
  • Effects of blocking drugs

11
Nerve Tissue
12
Membrane voltage
  • The main equation for stimulation of the Soma is
    always
  • I(st) I(io) C dV/dt
  • One part of the current loads the cell membrane
    capacity and the other part passes through the
    ion channels
  • Alternatively dV/dt I(st) I(io) /C
  • A positive stimulating current causes V to
    increase
  • To generate a spike this current must cause V to
    reach its threshold value

13
Threshold
  • Once the threshold voltage is reached many of the
    (sodium) ion channels open
  • The voltage increases to an action potential
    without the need for further stimulation
  • Once the threshold is reached the stimulus can be
    switched off
  • Alternatively, once the threshold is reached
    increasing the stimulating current further has
    little/no effect
  • But different cells have different threshold
    values depends on size of axons and somas

14
Axon models
  • Operation of axons have been modelled extensively
    for e.g. squid, frogs, rabbits and rats
  • An expression for human nerve fibres is given by
  • dV/dt -I(Na)-I(K)-I(L)I(st) /C
  • Where I(L) is a leakage current
  • Each current is then defined by means of a
    complex minimum (first) order equation

15
Temperature effects
  • Usually membrane model data is gathered at low
    temperatures
  • Raising the temperature generally causes a
    shortening of the action potential and an
    increase in spike propagation velocity
  • For temperatures higher than 31 to 33 degC action
    potentials no longer propagate in squid axons
  • In warm blooded animals spike durations shorten
    considerably but no heat block
  • Threshold levels change warmer means easier to
    excite!

16
(No Transcript)
17
Compartment models
  • Pieces of neuron can be treated as elements
  • A whole neuron is represented by an electrical
    network
  • Currents injected then can be treated with
    Kirchoffs law
  • Resistances become internal resistances of
    neighbouring compartments
  • Modeller must decide about degree of complexity
  • Much research in this area!

18
Model variability
  • Large variability in neuron models due partly to
    the large variability in neurons
  • Example absolute threshold current at the soma
    for a point source stimulation was
  • Passive model 32.9
    microA
  • Hodgkin-Huxley model 43
    microA
  • FCM(5 ion channels) model 71 microA
  • Compare with our studies (human)80 to 100 microA
  • Passive (based on RC) HH (based on squids)

19
Problems
  • Selective stimulation of neural tissue is an
    enormous challenge
  • Example in bladder control activation of the
    detrusor muscle without activation of the urethal
    sphincter
  • Every type of neuron exhibits different operating
    characteristics big problem in
    modelling/simulation
  • Neural geometry is complex, leading to complex
    models which require a high computational effort
    even for simple studies
  • External stimulation/monitoring very limited

20
(No Transcript)
Write a Comment
User Comments (0)
About PowerShow.com