TY - JOUR
T1 - Nothing can be coincidence
T2 - synaptic inhibition and plasticity in the cerebellar nuclei
AU - Pugh, Jason R.
AU - Raman, Indira M.
N1 - Funding Information:
Supported by the National Institutes of Health ( www.nih.gov ) NIH-NS39395 (I.M.R.). Studies of synaptic plasticity that form the focus of this review were also supported by F31-NS055542 (J.R.P.). We acknowledge members of the Raman laboratory who participated in the work from the laboratory cited in the review, Amy Gustafson, Dan Padgett, Petra Telgkamp, Tina Grieco, Zayd Khaliq and Teresa Aman, in addition to current laboratory members Nan Zheng, Abigail Person, Jason Bant and Mark Benton for discussions, and our collaborator and colleague Catherine Woolley.
PY - 2009/3
Y1 - 2009/3
N2 - Many cerebellar neurons fire spontaneously, generating 10-100 action potentials per second even without synaptic input. This high basal activity correlates with information-coding mechanisms that differ from those of cells that are quiescent until excited synaptically. For example, in the deep cerebellar nuclei, Hebbian patterns of coincident synaptic excitation and postsynaptic firing fail to induce long-term increases in the strength of excitatory inputs. Instead, excitatory synaptic currents are potentiated by combinations of inhibition and excitation that resemble the activity of Purkinje and mossy fiber afferents that is predicted to occur during cerebellar associative learning tasks. Such results indicate that circuits with intrinsically active neurons have rules for information transfer and storage that distinguish them from other brain regions.
AB - Many cerebellar neurons fire spontaneously, generating 10-100 action potentials per second even without synaptic input. This high basal activity correlates with information-coding mechanisms that differ from those of cells that are quiescent until excited synaptically. For example, in the deep cerebellar nuclei, Hebbian patterns of coincident synaptic excitation and postsynaptic firing fail to induce long-term increases in the strength of excitatory inputs. Instead, excitatory synaptic currents are potentiated by combinations of inhibition and excitation that resemble the activity of Purkinje and mossy fiber afferents that is predicted to occur during cerebellar associative learning tasks. Such results indicate that circuits with intrinsically active neurons have rules for information transfer and storage that distinguish them from other brain regions.
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U2 - 10.1016/j.tins.2008.12.001
DO - 10.1016/j.tins.2008.12.001
M3 - Review article
C2 - 19178955
AN - SCOPUS:61649106500
SN - 0166-2236
VL - 32
SP - 170
EP - 177
JO - Trends in Neurosciences
JF - Trends in Neurosciences
IS - 3
ER -