Efference copy

Efference copy
Efference copies are created with our own movement but not those of other people. This is why other people can tickle us (no efference copies of the movements that touch us) but we cannot tickle ourselves (efference copies tell us that we are stimulating ourselves).

Efference copy is an internal copy created with a motor command of its predicted movement and its resulting sensations. One role of efference copies is to enable the brain to estimate the sensory feedback from movements in which case they are called corollary discharges.

Efference copies are important in enabling motor adaptation such as to enhance gaze stability. They have a role in the perception of self and nonself electric fields in electric fish. They also underlie the phenomena of tickling.


Motor control

Motor signals

The efference copy is used to generate the predicted sensory feedback (corollary discharge) which estimate the sensory consequences of a motor command (top row). The actual sensory consequences of the motor command (bottom row) are used to compare with the corollary discharge to inform the CNS about external actions.

A motor signal from the central nervous system (CNS) to the periphery is called an efference, and a copy of this signal is called an efference copy. Sensory information coming from sensory receptors in the peripheral nervous system to the central nervous system is called afference. On a similar basis, nerves into the nervous system are afferent nerves and ones out are termed efferent nerves.

When an efferent signal is produced and sent to the motor system, it has been suggested that a copy of the signal, known as an efference copy, is created so that exafference (sensory signals generated from external stimuli in the environment) can be distinguished from reafference (sensory signals resulting from an animal's own actions).[1]

This efference copy by providing the input to a forward internal model is then used to generate the predicted sensory feedback that estimates the sensory consequences of a motor command. The actual sensory consequences of the motor command are then deployed to compare with the corollary discharge to inform the CNS about how well the expected action matched its actual external action.[2]

Corollary discharge

Corollary discharge is characterized as an afference copy of an action command used to inhibit any response to the self generated sensory signal which would interfere with the execution of the motor task. The inhibitory commands originate at the same time as the motor command and target the sensory pathway that would report any reafference to higher levels of the CNS. This is unique from the efference copy, since the corollary discharge is actually fed into the sensory pathway to cancel out the reafferent signals generated by the movement.[1] Alternatively, corollary discharges briefly alters self-generated sensory responses to reduce self-induced desensitization or help distinguish between self-generated and externally generated sensory information.[3]


von Helmholtz

The first person to propose the existence of efferent copies was the German physician and physicist Hermann von Helmholtz in the middle of the 19th century. He argued that the brain needed to create an efference copy for the motor commands that controlled eye muscles so as to aid the brain's determining the location of an object relative to the head. His argument used the experiment in which one gently presses on ones own eye. If this is done, one notices that the visual world seems to have "moved" as a result of this passive movement of the eye ball. In contrast, if the eye ball is actively moved by the eye muscles the world is perceived as still. The reasoning made is that with a passive movement of the eye ball, no efferent copies are made as with active movements that allow sensory changes to be anticipated and controlled for with the result in their absence the world appears to move.


In 1900, Charles Sherrington, the founder of modern ideas about motor control, rejected von Helmholtz ideas and argued that efference copies were not needed as muscles had their own sense of the movements they made. "The view [of von Helmholtz and his followers] which dispenses with peripheral organs and afferent nerves for the muscular sense has had powerful adherents . . . It supposes that during ... a willed movement the outgoing current of impulses from brain to muscle is accompanied by a 'sensation for innervation'. ... it "remains unproven".[4] This resulted in the idea of efference copies being dropped for the next 75 years.[5]

Von Holst

In 1950, Erich von Holst and Mittelstaedt investigated how species are able to distinguish between exafference and reafference given a seemingly identical percept of the two.[6] To explore this question, they rotated the head of a fly 180 degrees, effectively reversing the right and left edges of the retina and reversing the subject's subsequent reafferent signals. In this state, self-initiated movements of the fly would result in a perception that the world was also moving, rather than standing still as they would in a normal fly. After rotation of the eyes, the animal showed a reinforcement of the optokinetic response in the same direction as the moving visual input. Von Holst and Mittelstaedt interpreted their findings as evidence that corollary discharge (i.e. neural inhibition with active movement) could not have accounted for this observed change as this would have been expected to inhibit the optokinetic reaction. They concluded that an "Efferenzkopie" of the motor command was responsible for this reaction due to the persistence of the reafferent signal and given the consequent discrepancy between expected and actual sensory signals which reinforced the response rather than preventing it.[1][7]


The Nobel Prize winner, Roger Wolcott Sperry argued for the basis of corollary discharges following his research upon the optokinetic reflex.[8] He is also regarded as the originator of the term "corollary discharge".[9]

Motor adapation

The Coriolis effect

Efference copy relates to Coriolis effect in a manner that allows for learning and correction of errors experienced from unanticipated Coriolis forces. During self- generated rotational movements there is a learned CNS anticipation of Coriolis effects, mediated by generation of an appropriate efference copy that can be compared to re-afferent information.[10][11]

Gaze stability

It has been proposed that efference copy has an important role in maintaining gaze stability with active head movement by augmenting the vestibulo-ocular reflex (aVOR) during dynamic visual acuity testing.[12]

Grip Force

Efference copy within an internal model allows us to grip objects in parallel to a given load. In other words, the subject is able to properly grip any load that they are provided because the internal model provides such a good prediction of the object without any delay. Flanagan and Wing tested to see whether an internal model is used to predict movement-dependent loads by observing grip force changes with known loads during arm movements.[13] They found that even when giving subjects different known loads the grip force was able to predict the load force. Even when the load force was suddenly changed the grip force never lagged in the phase relationship with the load force, therefore affirming the fact that there was an internal model in the CNS that was allowing for the proper prediction to occur. It has been suggested by Kawato that for gripping, the CNS uses a combination of the inverse and forward model..[14] With the use of the efference copy the internal model can predict a future hand trajectory, thus allowing for the parallel grip to the particular load of the known object.


Experiments have been conducted wherein subjects' feet are tickled both by themselves and with a robotic arm controlled by their own arm movements. These experiments have shown that people find a self-produced tickling motion of the foot to be much less “tickly” than a tickling motion produced by an outside source. They have postulated that this is because when a person sends a motor command to produce the tickling motion, the efference copy anticipates and cancels out the sensory outcome. This idea is further supported by evidence that a delay between the self-produced tickling motor command and the actual execution of this movement (mediated by a robotic arm) causes an increase in the perceived tickliness of the sensation. This shows that when the efference copy is incompatible with the afference, the sensory information is perceived as if it were exafference. Therefore, it is theorized that it is not possible to tickle ourselves because when the predicted sensory feedback (efference copy) matches the actual sensory feedback, the actual feedback will be attenuated. If the predicted sensory feedback does not match the actual sensory feedback, whether caused by a delay (as in the mediation by the robotic arm) or by external influences from the environment, the brain cannot predict the tickling motion on the body and a more intense tickling sensation is perceived. This is the reason why one cannot tickle oneself.[15]

Mormyrid electric fish

In the mormyrid electric fish corollary discharges enables the knollenorgan sensor (KS) to detect the electric organ discharges of other fish without also detecting their own self generated electric organ discharges.

The mormyrid electric fish provides an example of corollary discharge in lower vertebrates.[3][16][17] Specifically, the knollenorgan sensor (KS) is involved with electro-communication, detecting the electric organ discharges (EOD) of other fish.[16][17] Unless the reafference was somehow modulated, the KS would also detect self generated EOD’s that would interfere with interpretation of external EOD’s needed for communication between fish. However, these fish display corollary discharges that inhibit the ascending sensory pathway at the first CNS relay point.[16][17] These corollary discharges are timed to arrive at the same time as the reafference from the KS to minimize the interference of self-produced EOD's with the perception of external EODs, and optimize the duration of inhibition.[17]


  1. ^ a b c Gallistel, CR (1980). The Organization of Action: A New Synthesis. Hillsdale: Lawrence Erlbaum Associates. pp. 166–209. ISBN 047026912X. 
  2. ^ Wolpert, DM; Miall RC (1996). "Forward Models for Physiological Motor Control". Neural Networks 9 (8): 1265–1279. doi:10.1016/S0893-6080(96)00035-4. PMID 12662535. 
  3. ^ a b Poulet, JFA; Hedwig B (2006). "New insights into corollary discharges mediated by identified neural pathways". TRENDS in Neuroscience 30 (1): 14–21. doi:10.1016/j.tins.2006.11.005. PMID 17137642. 
  4. ^ Sherrington CS. (1900). The muscular sense. In Textbook of Physiology, ed. E. A. Schafer, vol 2 pp. 1002-25. Edinburgh/London Pentland
  5. ^ Matthews PB. (1982). Where does Sherrington's "muscular sense" originate? Muscles, joints, corollary discharges? Annu Rev Neurosci.5:189-218.PubMed
  6. ^ von Holst E., Mittelstaedt H. (1950). The reafference principle. Interaction between the central nervous system and the periphery. In Selected Papers of Erich von Holst: The Behavioural Physiology of Animals and Man, London: Methuen. (From German) 1 : 1 39-73.
  7. ^ von Holst E. (1954). Relations between the central nervous system and the peripheral organs. Br. J. Animal Behav. 2:89-94
  8. ^ Sperry RW. (1950) Neural basis of the spontaneous optokinetic response produced by visual inversion. J Comp Physiol Psychol. Dec;43(6):482-9.PubMed
  9. ^ Jeannerod, Marc (2003): Action Monitoring and Forward Control of Movements. In: Michael Arbib (Ed.), The Handbook of Brain Theory and Neural Networks. Second Edition. Cambridge, Mass.: MIT Press, pp. 83–85, here: p. 83.
  10. ^ Cohn, JV; DiZio P, Lackner JR (1 June 2000). "Reaching during virtual rotation: context specific compensations for expected coriolis forces." (pdf). Journal of Neurophysiology 83 (6): 3230–3240. PMID 10848543. http://jn.physiology.org/cgi/reprint/83/6/3230. Retrieved 24 June 2008. 
  11. ^ Pigeon, P; Bortolami SB, DiZio P, Lackner JR (2003). "Coordinated turn and reach movements. II. Planning in an external frame of reference." (pdf). Journal of Neurophysiology 89 (1): 290–303. doi:10.1152/jn.00160.2001. PMID 12522180. http://jn.physiology.org/cgi/reprint/89/1/290. Retrieved 24 June 2008. 
  12. ^ Herdman, SJ; Schubert MC, Tusa RJ (2001). "Role of Central Preprogramming in Dynamic Visual Acuity With Vestibular Loss" (pdf). Arch Otolaryngol Head Neck Surg 127 (10): 1205–1210. PMID 11587600. http://archotol.ama-assn.org/cgi/reprint/127/10/1205. Retrieved 24 June 2008. 
  13. ^ Flanagan, R; Wing AM (15 February 1997). "The role of internal models in motion planning and control: evidence from grip force adjustments during movements of hand-held loads" (pdf). Journal of Neuroscience 17 (4): 1519–1528. PMID 9006993. http://www.jneurosci.org/cgi/reprint/17/4/1519. Retrieved 24 June 2008. 
  14. ^ Kawato, K (1999). "Internal models for motor control and trajectory planning". Current Opinion in Neurobiology 9 (6): 718–727. doi:10.1016/S0959-4388(99)00028-8. PMID 10607637. 
  15. ^ Blakemore, Sarah-Jayne; Wolpert, Daniel; Frith, Chris (August 2000). "Why can't you tickle yourself?" (pdf). NeoroReport 11 (11). http://learning.eng.cam.ac.uk/wolpert/publications/papers/BlaWolFri00.pdf. Retrieved 2008-02-20. 
  16. ^ a b c Bell, CC (1 September 1989). "Sensory coding and corollary discharge effects in mormyrid electric fish" (pdf). Journal of Experimental Biology 146 (1): 229–253. http://jeb.biologists.org/cgi/reprint/146/1/229. 
  17. ^ a b c d Bell, CC; Grant K (1 March 1989). "Corollary discharge inhibition and preservation of temporal information in a sensory nucleus of mormyrid electric fish" (pdf). The Journal of Neuroscience 9 (3): 1029–1044. PMID 2926477. http://www.jneurosci.org/cgi/reprint/9/3/1029. Retrieved 24 June 2008. 

Further reading

  • Arbib, Michael A. (1989): The Metaphorical Brain 2. Neural Networks and Beyond, New York: Wiley, pp. 23–26 [Section Corrolary Discharge], p. 33, pp. 297–299 [Section Control Systems for Saccade Generation].

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