TY - JOUR
T1 - GABA-A Inhibition Shapes the Spatial and Temporal Response Properties of Purkinje Cells in the Macaque Cerebellum
AU - Blazquez, Pablo M.
AU - Yakusheva, Tatyana A.
N1 - Funding Information:
We thank Drs. Stephen Highstein, Dora Angelaki, and Harold Barton for equipment and support; Dr. Yutaka Hirata and Shane Heiney for help editing the manuscript; Fanetta Hampton, Valentin Militchin, Krystal Henderson, and Darryl Craig for technical support and animal care; and Keith Graham and Buster Tipton of TORAY Carbon Fiber for supplying the carbon fibers. This work was funded by grants NINDS R01-NS065099 (to P.M.B.), the McDonnell Center for Higher Brain Function (to P.M.B.), NIDCD R03-DC011142 (to T.A.Y.), and NEI R01-EY012814 (to D.E.A.).
Publisher Copyright:
© 2015 The Authors.
PY - 2015/5/19
Y1 - 2015/5/19
N2 - Data from invitro and anesthetized preparations indicate that inhibition plays a major role in cerebellar cortex function. We investigated the role of GABA-A inhibition in the macaque cerebellar ventral-paraflocculus while animals performed oculomotor behaviors that are known to engage the circuit. We recorded Purkinje cell responses to these behaviors with and without application of gabazine, a GABA-A receptor antagonist, near the recorded neuron. Gabazine increased the neuronal responsiveness to saccades in all directions and the neuronal gain to VOR cancellation and pursuit, most significantly the eye and head velocity sensitivity. L-glutamate application indicated that these changes were not the consequence of increases in baseline firing rate. Importantly, gabazine did not affect behavior or efference copy, suggesting that only local computations were disrupted. Our data, collected while the cerebellum performs behaviorally relevant computations, indicate that inhibition is a potent regulatory mechanism for the control of input-output gain and spatial tuning in the cerebellar cortex.
AB - Data from invitro and anesthetized preparations indicate that inhibition plays a major role in cerebellar cortex function. We investigated the role of GABA-A inhibition in the macaque cerebellar ventral-paraflocculus while animals performed oculomotor behaviors that are known to engage the circuit. We recorded Purkinje cell responses to these behaviors with and without application of gabazine, a GABA-A receptor antagonist, near the recorded neuron. Gabazine increased the neuronal responsiveness to saccades in all directions and the neuronal gain to VOR cancellation and pursuit, most significantly the eye and head velocity sensitivity. L-glutamate application indicated that these changes were not the consequence of increases in baseline firing rate. Importantly, gabazine did not affect behavior or efference copy, suggesting that only local computations were disrupted. Our data, collected while the cerebellum performs behaviorally relevant computations, indicate that inhibition is a potent regulatory mechanism for the control of input-output gain and spatial tuning in the cerebellar cortex.
UR - http://www.scopus.com/inward/record.url?scp=84929705975&partnerID=8YFLogxK
U2 - 10.1016/j.celrep.2015.04.020
DO - 10.1016/j.celrep.2015.04.020
M3 - Article
C2 - 25959822
AN - SCOPUS:84929705975
SN - 2211-1247
VL - 11
SP - 1043
EP - 1053
JO - Cell Reports
JF - Cell Reports
IS - 7
ER -