The long-term goal of research proposed in the present application is to delineate neuronal systems and processes involved in simple forms of learning and memory. More specifically, this research seeks to advance our understanding of the involvement of the cerebellum in a simple motor learning task, classical eyelid conditioning in rabbits. Three experiments are proposed that use anesthetized classical conditioning preparations. These preparations involve the pairing of brain microstimulation in place of peripheral conditioning stimuli and recording unit activity from brain stem nuclei known to be involved in generating conditioning responses in place of monitoring overt behavioral responses. The proposed experiments include: (1) An analysis of extracellular single unit cerebellar activity during and after conditioning, (2) Manipulations of the """"""""behavioral"""""""" training regimen used during the anesthetized conditioning, and (3) Intracellular recordings coupled with HRP labeling after conditioning. These experiments have been designed to explore similarities and differences in conditioning between awake and anesthetized rabbits, to provide information about changes in the activity of cerebellar neurons induced by the anesthetized conditioning procedures, and to provide some insight into the connectivity between cerebellar and brain stem neurons involved in the conditioning. The further development of this anesthetized conditioning preparation should facilitate the definition and study of cerebellar and brain stem circuits activated during this form of learning. Intracellular analyses of neuronal activity should provide initial information about cellular processes and synaptic mechanisms associated with classical eyelid conditioning. We anticipate that these mechanisms may be generalizable to other motor learning and memory situations and therefore advance our understanding of basic cerebellar and brainstem neuronal function. Results from these experiments should also prove useful for understanding loss of normal function associated with cerebellar pathologies caused by injury or disease. Moreover, advancing our knowledge of cellular and synaptic processes involved in simple motor learning and memory should prove useful for understanding more complex learning and memory processes and the cellular bases of learning impairments and memory loss associated with disease and injury.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH051178-03
Application #
2034049
Study Section
Cognitive Functional Neuroscience Review Committee (CFN)
Project Start
1994-12-01
Project End
1998-11-30
Budget Start
1997-01-01
Budget End
1997-11-30
Support Year
3
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Indiana University Bloomington
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
006046700
City
Bloomington
State
IN
Country
United States
Zip Code
47401
Katz, Donald B; Rogers, Ronald F; Steinmetz, Joseph E (2002) Novel factors contributing to the expression of latent inhibition. Behav Neurosci 116:824-36
Katz, D B; Tracy, J A; Steinmetz, J E (2001) Rabbit classical eyeblink conditioning is altered by brief cerebellar cortical stimulation. Physiol Behav 72:499-510
Steinmetz, J E; Tracy, J A; Green, J T (2001) Classical eyeblink conditioning: clinical models and applications. Integr Physiol Behav Sci 36:220-38
Rogers, R F; Britton, G B; Steinmetz, J E (2001) Learning-related interpositus activity is conserved across species as studied during eyeblink conditioning in the rat. Brain Res 905:171-7
Churchill, J D; Green, J T; Voss, S E et al. (2001) Discrimination reversal conditioning of an eyeblink response is impaired by NMDA receptor blockade. Integr Physiol Behav Sci 36:62-74
Chen, G; Steinmetz, J E (2000) Microinfusion of protein kinase inhibitor H7 into the cerebellum impairs the acquisition but not the retention of classical eyeblink conditioning in rabbits. Brain Res 856:193-201
Chen, G; Steinmetz, J E (2000) Intra-cerebellar infusion of NMDA receptor antagonist AP5 disrupts classical eyeblink conditioning in rabbits. Brain Res 887:144-56
Banks, M K; Mohr, N L; Besheer, J et al. (1999) The effects of phenytoin on instrumental appetitive-to-aversive transfer in rats. Pharmacol Biochem Behav 63:465-72
Rogers, R F; Fender, A F; Steinmetz, J E (1999) The cerebellum is necessary for rabbit classical eyeblink conditioning with a non-somatosensory (photic) unconditioned stimulus. Behav Brain Res 104:105-12
Rogers, R F; Steinmetz, J E (1998) Contextually based conditional discrimination of the rabbit eyeblink response. Neurobiol Learn Mem 69:307-19

Showing the most recent 10 out of 12 publications