• Aucun résultat trouvé

Oculomotor control in human and non-human primates

N/A
N/A
Protected

Academic year: 2022

Partager "Oculomotor control in human and non-human primates"

Copied!
30
0
0

Texte intégral

(1)

Oculomotor control in human and non-human primates

Tymothée Poitou, Matthew J. Nelson, Hadrien Caron, Pauline Espi, Nicolas Wattiez, Sophie Rivaud-Péchoux,

Bertrand Gaymard and Pierre Pouget

CR-ICM, Paris, France

GT8 Robotique/Neurosciences June 23th 2011

(2)
(3)

Eye movements are under voluntary control

Yarbus (1967)

(4)

Eye movements are under voluntary control

Yarbus (1967) “Remember the location of objects in the room”

Eye movements are under voluntary control

(5)

Eye movements are under voluntary control

“Remember the

ages of the people in the room”

Yarbus (1967) “Remember the location of objects in the room”

Eye movements are under voluntary control

(6)

How does the brain choose where to look?

How does the brain correct errors?

How does the brain control when to move?

(7)

Work on saccadic reaction times in humans seems to suggest that the brain runs a kind of race between signals representing different possible targets, with more probable targets starting nearer the

finishing post than less probable ones.

There is also a huge random element, rather like a gratuitous random handicap, so that reaction times are very variable even when the stimuli and conditions are absolutely constant.

This may well represent a deliberate mechanism for making sure our behaviour is not too predictable by our predators (and you may like to think of it as the neural mechanism behind our illusion of 'free will’.

Roger Carpenter: http://babylon.acad.cai.cam.ac.uk/people/rhsc/oculo.html

(8)

A race between signals representing different possible targets…

Théodore Géricault, 1791-1824

(9)

How to stop the race?

Théodore Géricault, 1791-1824

(10)

Stopping oculomotor plans in human

and non-human primates

(11)

Stopping oculomotor plan

(12)
(13)

Countermanding Task

(14)

Race model of behavior

(Logan and Cowan, 1984)

(15)

Visual Cortex

LGN

RF

Saccade Thalamus

Cerebellum

SCi SCs Frontal cortex

(DLPFC, ACC, SEF)

Parietal Cortex (LIP)

Retina

Temporal Cortex (TEO)

FEF

Basal Ganglia

Saccades are produced by a distributed network

(16)

Spatial selectivity of the motor signal

§  Movement activity is spatially tuned.

(e.g. Russo and Bruce, 1993)

(17)

§  How selective is the inhibitory signal?

Contralateral visual inhibition.

Inhibitory local connections.

Selectivity of the inhibitory signal

§  How flexible is the inhibitory signal?

(Pouget et al., 2005, 2009)

(18)

Spatial selectivity of inhibitory signal(s)

(19)

Inhibition function

§ How to calculate the inhibition function?

Cancelled (C)

P(Non-Cancelled/SSD)

(20)

Stop Signal Reaction Time

§  Estimate the Stop Signal Reaction Time (SSRT)

SSRT is the delay before, which saccades are cancelled and

after, which saccades are produced…

(21)

Spatial selectivity of the inhibitory signal

§  How flexible is the inhibitory signal?

(22)

20 40 50 60 80

−150

−100

−50 0 50 100 150

Percent of right stop

HUMAN Latencies (ms)

20 40 50 60 80 −150

−100

−50 0 50 100 150

MONKEY Latencies (ms)

20 40 50 60 80

−175

−125

−75

−25 0 25 75 125 175

Percent of right stop

HUMAN SSRT (ms)

20 40 50 60 80 −175

−125

−75

−25 0 25 75 125 175

MONKEY SSRT (ms)

Selectivity of the inhibitory signal

Variations of probability of stop trials are tracked by the inhibitory system.

RTs and SSRT can be spatially tuned.

Reaction times increase as function as the lateralized probability of stop

trials increases

SSRT decreases as function as the lateralized probability of stop

trials increases

Human (Right - Left) saccade latency (ms) Human (Right - Left) SSRT (ms)

% of stop trials Right/Target

Monkey (Right - Left) saccade latency (ms) Monkey (Right - Left) SSRT (ms)

% of stop trials Right/Target

(23)

Time course of spatial selectivity…

0 500 1000 1500

180 200 220 240 260 280 300 320

200 300 250

0 500 1000 1500 0 50 100 150 200 250 300

300 350 400 450 500 550

300 400 500

0 100 200 300

200 300 250

0 500 1000 1500 0 100 200 300

300 400 500

Monkey Human

N = 221

Latencies (ms)

Trials

Latencies (ms)

Trials

N = 56

Variations of probability of stop trials are tracked with sub-optimal adjustments of response times...

(24)

Selectivity of the inhibitory signal

(1)  The inhibitory signal is spatially tuned.

(2)  Modest variations of probability of stop trials are tracked by the

inhibitory system.

(25)

Spatial selectivity of the inhibitory signal

Spatial manipulations of probability of stop trials:

Opposite hemifield: 180° Opposite hemifield: 30° / 5° Same hemifield: 30° / 5°

Target 1.5° x 1.5° at 12° eccentricity

(26)

Probabilities of stop trials -associated with each target- are tracked unless targets are separated by less than 10° of visual angle.

Spatial selectivity of the inhibitory signal

(27)

What is controlling these inhibitory signals?

(Boucher et al., 2007)

(28)
(29)

Thank you

GT8 Robotique/Neurosciences June 23th 2011

(30)

Références

Documents relatifs

Abstract – Background: Several cases of infections due to Echinococcus multilocularis, Taenia martis and Taenia crassiceps were recently described in various species of

Gustatory perception is usually assessed by a measurement of taste thresholds (i.e. the minimum perceived concentration of a taste stimulus) and supra-threshold taste

Allometric relationship between the area of the absorptive mucosa of the digestive tract and functional body size in three distinct group of species, according to major

Such learning processes are preva- lent during the exploratory phase in development. 34 Young children, after watching a respected older child eat a particular dish ,

Un devis pré-expérimental incluant un pré-test et un post-test a été utilisé pour réaliser cette étude pilote visant à évaluer les effets du programme « Apprentissage à

These results provide new evidence on the dynamics of chunking processes in non-human primates and, more generally, on the mechanisms involved in implicit statistical learning, a

Conversely, the occurrence of alkaloids, tannins, and various other more or less toxic compounds in plants should have co-evolved with the ability of primates (and other

The substantial literature on OT effects in the nucleus accumbens and its interaction with dopamine and opioids makes it clear that OT is an important regulator of social