In the last decade, the physiology of cerebellar neurons and synapses has been extended to a considerable extent. We have found that the mossy fiber-granule cell relay can generate a complex form of long-term potentiation (mf-GrC LTP) following high-frequency mf discharge. Induction. Mf-GrC LTP depends on NMDA and mGlu receptor activation, intracellular Ca(2+) increase, PKC activation, and NO production. The preventative action of intracellular agents (BAPTA, PKC-inhibitors) and of membrane hyperpolarization, and the correlated increase in intracellular Ca(2+) observed using fluorescent dyes, indicate that induction occurs postsynaptically. Expression. Expression includes three components: (a) an increase of synaptic currents, (b) an increase of intrinsic excitability in GrC, and (c) an increase of intrinsic excitability in mf terminals. Based on quantal analysis, the EPSC increase is mostly explained by enhanced neurotransmitter release. NO is a candidate retrograde neurotransmitter which could determine both presynaptic current changes and LTP. NO cascade blockers inhibit both presynaptic current changes and LTP. The increase in intrinsic excitability involves a raise in apparent input resistance in the subthreshold region and a spike threshold reduction. Together with other forms of cerebellar plasticity, mf-GrC LTP opens new hypothesis on how the cerebellum processes incoming information

Long-term potentiation of synaptic transmission at the mossy fiber-granule cell relay of cerebellum

D'ANGELO, EGIDIO UGO;ROSSI, PAOLA;PRESTORI, FRANCESCA;
2005-01-01

Abstract

In the last decade, the physiology of cerebellar neurons and synapses has been extended to a considerable extent. We have found that the mossy fiber-granule cell relay can generate a complex form of long-term potentiation (mf-GrC LTP) following high-frequency mf discharge. Induction. Mf-GrC LTP depends on NMDA and mGlu receptor activation, intracellular Ca(2+) increase, PKC activation, and NO production. The preventative action of intracellular agents (BAPTA, PKC-inhibitors) and of membrane hyperpolarization, and the correlated increase in intracellular Ca(2+) observed using fluorescent dyes, indicate that induction occurs postsynaptically. Expression. Expression includes three components: (a) an increase of synaptic currents, (b) an increase of intrinsic excitability in GrC, and (c) an increase of intrinsic excitability in mf terminals. Based on quantal analysis, the EPSC increase is mostly explained by enhanced neurotransmitter release. NO is a candidate retrograde neurotransmitter which could determine both presynaptic current changes and LTP. NO cascade blockers inhibit both presynaptic current changes and LTP. The increase in intrinsic excitability involves a raise in apparent input resistance in the subthreshold region and a spike threshold reduction. Together with other forms of cerebellar plasticity, mf-GrC LTP opens new hypothesis on how the cerebellum processes incoming information
2005
CREATING COORDINATION IN THE CEREBELLUM
DeZeeuw, CI; Cicirata, F
Physiology considers resources that study the regulation of biological functions at the level of the whole organism. This includes research from biochemical, cell biological and whole system studies of human and animal physiology. Comparative physiology, biological rhythms, and physiological measurement are also included. Resources emphasizing cellular regulation, or the physiology of specific organs are excluded and are covered in the Cell & Developmental Biology and Medical Research: Organs & Systems categories.
Sì, ma tipo non specificato
Inglese
Internazionale
STAMPA
148
69
80
12
0-444-51754-5
Elsevier Science BV
Amsterdam
PAESI BASSI
reviews of reference for neuroscience - PMID 15661182
cerevelleto; strato granulare; plasticità sinaptica; LTP
http://www-1.unipv.it/dsffcm/pagine/labs/dangelo/publish.html
2 Contributo in Volume::2.1 Contributo in volume (Capitolo o Saggio)
7
268
none
D'Angelo, EGIDIO UGO; Rossi, Paola; Gall, D.; Prestori, Francesca; Nieus, T.; Maffei, A.; Sola, E.
info:eu-repo/semantics/bookPart
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/114284
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