TY - JOUR
T1 - Using input minimization to train a cerebellar model to simulate regulation of smooth pursuit
AU - Rothganger, Fredrick H.
AU - Anastasio, Thomas J.
N1 - Funding Information:
Supported in part by the Laboratory Directed Research and Development program at Sandia National Laboratories. Sandia is a multiprogram laboratory operated by Sandia Corporation, a Lockheed Martin Company, for the United States Department of Energy’s National Nuclear Security Administration under Contract DE-AC04-94AL85000.
PY - 2009/12
Y1 - 2009/12
N2 - Cerebellar learning appears to be driven by motor error, but whether or not error signals are provided by climbing fibers (CFs) remains a matter of controversy. Here we show that a model of the cerebellum can be trained to simulate the regulation of smooth pursuit eye movements by minimizing its inputs from parallel fibers (PFs), which carry various signals including error and efference copy. The CF spikes act as "learn now" signals. The model can be trained to simulate the regulation of smooth pursuit of visual objects following circular or complex trajectories and provides insight into how Purkinje cells might encode pursuit parameters. In minimizing both error and efference copy, the model demonstrates how cerebellar learning through PF input minimization (InMin) can make movements more accurate and more efficient. An experimental test is derived that would distinguish InMin from other models of cerebellar learning which assume that CFs carry error signals.
AB - Cerebellar learning appears to be driven by motor error, but whether or not error signals are provided by climbing fibers (CFs) remains a matter of controversy. Here we show that a model of the cerebellum can be trained to simulate the regulation of smooth pursuit eye movements by minimizing its inputs from parallel fibers (PFs), which carry various signals including error and efference copy. The CF spikes act as "learn now" signals. The model can be trained to simulate the regulation of smooth pursuit of visual objects following circular or complex trajectories and provides insight into how Purkinje cells might encode pursuit parameters. In minimizing both error and efference copy, the model demonstrates how cerebellar learning through PF input minimization (InMin) can make movements more accurate and more efficient. An experimental test is derived that would distinguish InMin from other models of cerebellar learning which assume that CFs carry error signals.
KW - Cerebellum
KW - Computational model
KW - Learning
KW - Smooth pursuit
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U2 - 10.1007/s00422-009-0340-7
DO - 10.1007/s00422-009-0340-7
M3 - Article
C2 - 19937072
AN - SCOPUS:72149097859
SN - 0340-1200
VL - 101
SP - 339
EP - 359
JO - Biological Cybernetics
JF - Biological Cybernetics
IS - 5-6
ER -