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Christian
Hansel, Ph.D. |
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Cellular mechanisms of
plasticity in the cerebellum. In Marr-Albus-Ito
models of cerebellar function, coactivation
of the climbing fiber (CF) synapse, which provides massive, invariant
excitation of Purkinje neurons (coding the unconditioned stimulus), together
with a graded parallel fiber synaptic array (coding the conditioned stimulus)
leads to long-term depression (LTD) of parallel fiber (PF)-Purkinje cell (PC)
synapses, underlying production of a conditioned response. PF-LTD is
generally assumed to provide the cellular basis for several forms of cerebellar motor learning. In my lab, we examine cellular mechanisms underlying
long-term potentiation (LTP) and LTD at PF-PC
synapses as well as LTD at CF-PC synapses. We have recently shown that bidirectional plasticity
at PF synapses is governed by induction rules that operate inverse to their
counterparts at e.g. hippocampal synapses:
Another
unique feature of cerebellar plasticity is that LTP
and LTD at PF synapses are under control of the heterosynaptic
CF input. Moreover, previous CF-LTD induction reduces the probability of
subsequent PF-LTD induction. A new line of research focuses on
activity-dependent changes in the intrinsic excitability of Purkinje cells.
Moreover, we try to characterize how clinically relevant substances, which
negatively (alcohol) or positively (memory-enhancers, such as ampakines) interfere with AMPA receptor-mediated
transmission, affect cerebellar plasticity and
learning. Experimentally, we use whole-cell patch-clamp recordings from PCs
in rat or mouse cerebellar slices. In some
experiments, we combine the electrophysiological recordings with microfluorometric imaging techniques using a cooled CCD
camera.
Last updated 08/27/09 |
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