| Preface |
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1 Cerebellar long-term depression as investigated in a cell culture preparation |
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1 | (8) |
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2 Cellular mechanisms of long-term depression in the cerebellum |
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9 | (7) |
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3 Long-lasting potentiation of GABAergic inhibitory synaptic transmission in cerebellar Purkinje cells: Its properties and possible mechanisms |
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16 | (8) |
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4 Nitric oxide and synaptic plasticity: NO news from the cerebellum |
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24 | (6) |
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5 Models of the cerebellum and motor learning |
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30 | (16) |
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6 On climbing fiber signals and their consequence(s) |
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46 | (15) |
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7 Does the cerebellum learn strategies for the optimal time-varying control of joint stiffness? |
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61 | (12) |
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8 On the specific role of the cerebellum in motor learning and cognition: Clues from PET activation and lesion studies in man |
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73 | (23) |
| Open Peer Commentary and Authors' Responses |
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96 | (71) |
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96 | (2) |
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98 | (48) |
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Spanning the levels in cerebellar function |
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98 | (1) |
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Similarities and contrasts between cerebellar LTD and hippocampal LTP |
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99 | (1) |
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What has to be learned in motor learning? |
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100 | (1) |
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How and where does nitric oxide affect cerebellar synaptic plasticity? New methods for investigating its action |
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101 | (1) |
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Perhaps it's time to completely rethink cerebellar function |
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102 | (1) |
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Long-term changes of synaptic transmission: A topic of long-term interest |
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103 | (1) |
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One cannot build theories of cerebellar function on shaky foundations: Induction properties of long-term depression have to be taken into account |
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104 | (1) |
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Saccades and the adjustable pattern generator |
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105 | (1) |
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How can the cerebellum match "error signal" and "error correction?" |
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106 | (1) |
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Grasping cerebellar function depends on our understanding the principles of sensorimotor integration: The frame of reference hypothesis |
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106 | (3) |
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Timing implications of metabotropic mechanisms for cerebellar learning |
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109 | (2) |
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The cerebellum as comparator: Increases in cerebellar activity during motor learning may reflect its role as part of an error detection correction mechanism |
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111 | (1) |
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Cerebellum does more than recalibration of movements after perturbations |
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112 | (1) |
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How and what does the cerebellum learn? |
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113 | (1) |
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Is stiffness a byproduct or a target? |
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114 | (1) |
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What can and what cannot be adjusted in the movement pattern of cerebellar patients? |
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115 | (2) |
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The role of the cerebellum in motor learning is limited |
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117 | (1) |
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Two separate pathways for cerebellar LTD: NO-dependent and NO-independent |
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117 | (2) |
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Programming the cerebellum |
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119 | (1) |
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Positive cerebellar feedback loops |
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119 | (1) |
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Molecules involved in cerebellar long-term depression (LTD) and mutant mice defective in it |
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120 | (1) |
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Cerebellar arm ataxia: Theories still have a lot to explain |
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121 | (1) |
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Computational significance of the cellular mechanisms for synaptic plasticity in Purkinje cells |
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121 | (4) |
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Constructing a theory of cerebellar function in limb movement control is premature |
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125 | (1) |
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New players for cerebellar long-term depression |
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126 | (1) |
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The common inverse-dynamics motor-command coordinates for complex and simple spikes |
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126 | (2) |
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Which cerebellar cells contribute to extracellular cGMP? |
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128 | (1) |
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The notions of joint stiffness and synaptic plasticity in motor memory |
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129 | (1) |
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Sensory prediction as a role for the cerebellum |
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130 | (1) |
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Further evidence for the involvement of nitric oxide in trans-ACPD-induced suppression of AMPA responses in cultured chick Purkinje neurons |
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131 | (1) |
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Nitric oxide is involved in cerebellar long-term depression |
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132 | (1) |
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The cerebellum and cerebral cortex: Contrasting and converging contributions to spatial navigation and memory |
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133 | (1) |
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Cerebellar theory out of control |
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134 | (1) |
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Cerebellar rhythms: Exploring another metaphor |
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135 | (1) |
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Dysmetria of thought: Correlations and conundrums in the relationship between the cerebellum, learning, and cognitive processing |
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136 | (2) |
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How to link the specificity of cerebellar anatomy to motor learning? |
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138 | (1) |
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We know a lot about the cerebellum, but do we know what motor learning is? |
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138 | (1) |
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Motor learning and synaptic plasticity in the cerebellum |
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139 | (2) |
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Limitations of PET and lesion studies in defining the role of the human cerebellum in motor learning |
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141 | (1) |
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Sensorimotor learning in structures "upstream" from the cerebellum |
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141 | (1) |
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What behavioral benefit does stiffness control have? An elaboration of Smith's proposal |
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142 | (1) |
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Eyeblink conditioning, motor control, and the analysis of limbic-cerebellar interactions |
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143 | (2) |
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Plasticity of cerebro-cerebellar interactions in patients with cerebellar dysfunction |
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145 | (1) |
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146 | (21) |
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A cerebellar long-term depression update |
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146 | (6) |
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Cellular mechanisms of long-term depression: From consensus to open questions |
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152 | (1) |
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A bridge between cerebellar long-term depression and discrete motor learning: Studies on gene knockout mice |
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152 | (2) |
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NO more news from the cerebellum |
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154 | (2) |
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More models of the cerebellum |
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156 | (4) |
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More on climbing fiber signals and their consequence(s) |
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160 | (3) |
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Resilient cerebellar theory complies with stiff opposition |
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163 | (2) |
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Q: Is the cerebellum an adaptive combiner of motor and mental motor activites? A: Yes, maybe, certainly not, who can say? |
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165 | (2) |
| References |
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167 | (26) |
| Index |
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193 | |