Title: Lecture 4: Motor Control
1Lecture 4Motor Control
- Prof.dr. Jaap Murre
- University of Maastricht
- University of Amsterdam
- jaap_at_murre.com
- http//neuromod.org
2Overview
- The anatomy of the motor system
- Population coding
- The role of spinal cord, cerebellum, and basal
ganglia - This is not in the book, but can be on exam anyway
3Muscles are activated by alpha motor neurons
4The stretch reflex reveals some elementary
processing in the spinal cord
5Cortical anatomy of the motor system lateral view
6Medial view
7Schematic overview of the motor system
8Basic questions regarding motor control can
nowadays be answered
- How are motor movements represented in the brain?
- How are they used in the production of movement?
- Which brain areas are involved?
9How to be precise with noisy components
Area 5 neuron during repeated reaching movements
each individual trial gives a rather imprecise
signal
10Population coding
- Population coding allows precise representations
on the basis of (very) noisy or even damaged
components - Population coding is based on the statistics of
averages - They rely on coarse-coded neural representations
11Coarse coding
- If a neurons representation responds to many
inputs, this is called coarse coding - The advantage is that more accurate
representations can be formed by suitable
combination of the coarse representations
12Why coarse coding works
- If we move along a straight line, each time we
cross a receptive field boundary one neurons
changes its activation - the representation changes.
13In primates abundant evidence exists for coarse
coding
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17Georgopoulos shows that movement is coded in
population vectors
18Population vectors give accurate movement
direction signals
19Motor cortex sets up the signal, but execution is
dependent upon other areas
20Original plans in motor cortex are sometimes
revised on the go
21Activation of motor areas is a cascade rather
than a sequence
22Simple movement activations motor cortex and
somatosensory cortex
23More complicated sequences involve other areas
SMA supplementary motor area (part of area 6)
24Imagined movements remain limited to the
supplementary motor area (SMA)
25Internally and externally generated movements
PMC premotor cortex (also part of area 6)
26Skilled (Old) versus new motor movements
27Response competition
28Elastic constraints in motor development
- The problem of grasping is overdetermined given
an end-location, many possible joint positions
solve the problem - In order to make the problem soluble elastic
constraints are necessary (cf. Mike Jordan) - Muscles (as springs) are one source of such
constraints
29Spinal cord
30Coarse maps of limb movements in the frog
- Spinal cord of frogs does significant motor
processing - Frog can still clean itself after severing of
cord (dogs can also still scratch themselves) - The data suggest that even at a spinal level
coarse coding is used - It is likely that similar types of coding are
used in mammals
31Cats with severed spinal cord could still walk on
a treadmill
32Method followed by Emilio Bizzi
Based on the idea of muscles as springs by
Feldman
33Limb movements in frog spinal cord are coded with
respect to their end-positions
34The interactions of force fields can be described
by vector calculus
Fields A and B combined predict field ltABgt (see
C). When A and B are stimulated the resulting
field (see D) corresponds to the theoretical
field ltABgt
35Cerebellum
36Glickstein it is not completely clear what the
cerebellum does
- Bimanual control
- Motor learning?
- vestibuloocular reflex
- nictitating membrane response
- Coordination and integration of movements
37Global anatomy of cerebellum
38More detailed anatomy of cerebellum
39Louis Bolk midline cerebellar vernis controls
bilaterally synchronized movements cerebellar
hemispheres control unilateral movements
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41David Marr (1969) cerebellum is excellent for
simple associative learning (conditioning)
42Hebb-Marr networks
- Marrs views can be combined with those of Hebb
to yield associative networks - These networks can store input-output patterns
(hetero-associative learning) - The exhibit
- pattern completion or content-addressable memory
- fault tolerance
43Willshaw networks
- Highly abstracted, early neural network from 1969
- Activations are 0 or 1
- A weight either has the value 0 or 1
- A weight is set to 1 if input and output are 1
- At retrieval the net input is divided by the
total number of active nodes in the input pattern
44Example of a simple heteroassociative memory of
the Willshaw type
1 0 0 1 1 0
0 0 1 0 1 1
1 1 0 1 0 0
0 0 0 1 1 1
1 1 1 1 1 1 1 1 1
1 0 1 0 1 0
0 0 1 0 1 1
1 1 1 1 1 1 1 1 1
1 1 1 1 1 1 1 1 1
45Example of pattern retrieval
(1 0 0 1 1 0)
1 1 1 1 1 1 1 1 1
0 0 1 0 1 1
1 1 1 1 1 1 1 1 1
1 1 1 1 1 1 1 1 1
3 2 2 3 3 2
Sum 3
1 0 0 1 1 0
Div by 3
46Example of successful pattern completion using a
subpattern
(1 0 0 1 1 0)
1 1 1 1 1 1 1 1 1
0 0 1 0 0 1
1 1 1 1 1 1 1 1 1
1 1 1 1 1 1 1 1 1
1
2 1 1 2 2 1
Sum 2
1 0 0 1 1 0
Div by 2
47Example graceful degradation small lesions have
small effects
(1 0 0 1 1 0)
1 1 1 1 1 1 1 1 1
0 0 1 0 1 1
1 1 1 1 1
1 1 1 1 1 1 1 1
3 2 1 2 3 1
Sum 3
1 0 0 0 1 0
Div by 3
48Correspondence views on brain structures
49Computational views on cerebellum
50Summary
- Like vision, motor behavior has a lot of special
purpose circuitry - We can understand many aspects of this circuitry
in terms of why this representation makes sense - For example, coarse grained coding has the
advantage of precise control despite noisy
components
51Summary (continued)
- Motor behavior is not simply stringing together
some basic movements - Motor planning and execution are very much
cognitive functions