Literature DB >> 12867530

Developmental changes in evoked Purkinje cell complex spike responses.

Daniel A Nicholson1, John H Freeman.   

Abstract

The development of synaptic interconnections between the cerebellum and inferior olive, the sole source of climbing fibers, could contribute to the ontogeny of certain forms of motor learning (e.g., eyeblink conditioning). Purkinje cell complex spikes are produced exclusively by climbing fibers and exhibit short- and long-latency activity in response to somatosensory stimulation. Previous studies have demonstrated that evoked short- and long-latency complex spikes generally occur on separate trials and that this response segregation is regulated by inhibitory feedback to the inferior olive. The present experiment tested the hypothesis that complex spikes evoked by periorbital stimulation are regulated by inhibitory feedback from the cerebellum and that this feedback develops between postnatal days (PND) 17 and 24. Recordings from individual Purkinje cell complex spikes in urethan-anesthetized rats indicated that the segregation of short- and long-latency evoked complex spike activity emerges between PND17 and PND24. In addition, infusion of picrotoxin, a GABAA-receptor antagonist, into the inferior olive abolished the response pattern segregation in PND24 rats, producing evoked complex spike response patterns similar to those characteristic of younger rats. These data support the view that cerebellar feedback to the inferior olive, which is exclusively inhibitory, undergoes substantial changes in the same developmental time window in which certain forms of motor learning emerge.

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Year:  2003        PMID: 12867530     DOI: 10.1152/jn.00481.2003

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  13 in total

1.  Developmental changes in the neural mechanisms of eyeblink conditioning.

Authors:  John H Freeman; Daniel A Nicholson
Journal:  Behav Cogn Neurosci Rev       Date:  2004-03

2.  Pontine stimulation overcomes developmental limitations in the neural mechanisms of eyeblink conditioning.

Authors:  John H Freeman; Christine A Rabinak; Matthew M Campolattaro
Journal:  Learn Mem       Date:  2005 May-Jun       Impact factor: 2.460

3.  Selective developmental increase in the climbing fiber input to the cerebellar interpositus nucleus in rats.

Authors:  Daniel A Nicholson; John H Freeman
Journal:  Behav Neurosci       Date:  2004-10       Impact factor: 1.912

4.  Inferior olive oscillation as the temporal basis for motricity and oscillatory reset as the basis for motor error correction.

Authors:  R R Llinás
Journal:  Neuroscience       Date:  2009-04-22       Impact factor: 3.590

Review 5.  Cerebellar motor learning versus cerebellar motor timing: the climbing fibre story.

Authors:  Rodolfo R Llinás
Journal:  J Physiol       Date:  2011-03-28       Impact factor: 5.182

6.  Associative plasticity in the medial auditory thalamus and cerebellar interpositus nucleus during eyeblink conditioning.

Authors:  Hunter E Halverson; Inah Lee; John H Freeman
Journal:  J Neurosci       Date:  2010-06-30       Impact factor: 6.167

7.  Cerebellar inhibitory output shapes the temporal dynamics of its somatosensory inferior olivary input.

Authors:  Roni Hogri; Eyal Segalis; Matti Mintz
Journal:  Cerebellum       Date:  2014-08       Impact factor: 3.847

8.  Eyeblink conditioning in rats using pontine stimulation as a conditioned stimulus.

Authors:  John H Freeman; Christine A Rabinak
Journal:  Integr Physiol Behav Sci       Date:  2004 Jul-Sep

Review 9.  Neural circuitry and plasticity mechanisms underlying delay eyeblink conditioning.

Authors:  John H Freeman; Adam B Steinmetz
Journal:  Learn Mem       Date:  2011-10-03       Impact factor: 2.460

10.  REM sleep twitches rouse nascent cerebellar circuits: Implications for sensorimotor development.

Authors:  Greta Sokoloff; Brandt D Uitermarkt; Mark S Blumberg
Journal:  Dev Neurobiol       Date:  2014-04-25       Impact factor: 3.964

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