|
|
||||||||
The Journal of Neurophysiology Vol. 81 No. 3 March 1999, pp. 1242-1250
Copyright ©1999 by the American Physiological Society
Neuroscience Group, Division of Basic Biomedical Sciences, University of South Dakota School of Medicine, Vermillion, South Dakota 57069
Anderson, Curtis W. and
Joyce Keifer.
Properties of conditioned abducens nerve responses in a highly reduced
in vitro brain stem preparation from the turtle. Previous work
suggested that the cerebellum and red nucleus are not necessary for the
acquisition, extinction, and reacquistion of the in vitro classically
conditioned abducens nerve response in the turtle. These findings are
extended in the present study by obtaining conditioned responses (CRs)
in preparations that received a partial ablation of the brain stem
circuitry. In addition to removing all tissue rostral to and including
the midbrain and cerebellum, a transection was made just caudal to the
emergence of the IXth nerve. Such ablations result in a 4-mm-thick
section of brain stem tissue that functionally eliminates the sustained
component of the unconditioned response (UR) while leaving only a
phasic component. We refer to this region of brain stem tissue caudal to the IXth nerve as the "caudal premotor blink region." Neural discharge was recorded from the abducens nerve following a single shock
unconditioned stimulus (US) applied to the ipsilateral trigeminal nerve. When the US was paired with a conditioned stimulus (CS) applied
to the posterior eighth, or auditory, nerve using a delay conditioning
paradigm, a positive slope of CR acquisition was recorded in the
abducens nerve, and CR extinction was recorded when the stimuli were
alternated. Resumption of paired stimuli resulted in reacquisition.
Quantitative analysis of the CRs in preparations in which the caudal
premotor blink region had been removed and those with cerebellar/red
nucleus lesions showed that both types of preparations had abnormally
short latency CR onsets compared with preparations in which these
regions were intact. Preparations with brain stem transections had
significantly earlier CR offsets as more CRs terminated as short bursts
when compared with intact or cerebellar lesioned preparations. These
data suggest that a highly reduced in vitro brain stem preparation from
the turtle can be classically conditioned. Furthermore, the caudal brain stem is not a site of acquisition in this reduced preparation, but it contributes to the sustained activity of both the UR and CR.
Finally, the unusually short CR onset latencies following lesions to
the cerebellum are not further exacerbated by removal of the caudal
brain stem. These studies suggest that convergence of CS and US
synaptic inputs onto the abducens nerve reflex circuitry may underlie
acquisition in this reduced preparation, but that mechanisms that
control learned CR timing arise from the cerebellorubral system.
This article has been cited by other articles:
![]() |
Z. Zheng and J. Keifer PKA Has a Critical Role in Synaptic Delivery of GluR1- and GluR4-Containing AMPARs During Initial Stages of Acquisition of In Vitro Classical Conditioning J Neurophysiol, May 1, 2009; 101(5): 2539 - 2549. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Mokin, Z. Zheng, and J. Keifer Conversion of Silent Synapses Into the Active Pool by Selective GluR1-3 and GluR4 AMPAR Trafficking During In Vitro Classical Conditioning J Neurophysiol, September 1, 2007; 98(3): 1278 - 1286. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Keifer, Z.-Q. Zheng, and D. Zhu MAPK Signaling Pathways Mediate AMPA Receptor Trafficking in an In Vitro Model of Classical Conditioning J Neurophysiol, March 1, 2007; 97(3): 2067 - 2074. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Mokin, J. S. Lindahl, and J. Keifer Immediate-Early Gene-Encoded Protein Arc Is Associated With Synaptic Delivery of GluR4-containing AMPA Receptors During In Vitro Classical Conditioning J Neurophysiol, January 1, 2006; 95(1): 215 - 224. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Mokin and J. Keifer Expression of the immediate-early gene-encoded protein Egr-1 (zif268) during in vitro classical conditioning Learn. Mem., March 1, 2005; 12(2): 144 - 149. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Keifer In Vitro Eye-Blink Classical Conditioning Is NMDA Receptor Dependent and Involves Redistribution of AMPA Receptor Subunit GluR4 J. Neurosci., April 1, 2001; 21(7): 2434 - 2441. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |