This request for an ADAMHA RSDA is intended to facilitate the career developmenbt of a scientist whose research is focusedin the are of brain mechanisms underlying learning and memory. Previous research has implicated opioid peptide and norepinephrine (NE) systems in learning and memory processes. More specifically, the results of many studies which have assessed the effects of post-conditioning manipulations of opiate and NE activity have indicated that opiate and NE systems appear to exert opposing effects on retention of conditioning. Through the use of intracranial pharmacological injecton techniques, we have observed that at least a component of the opiate sensitive and NE systems which affect mamory processes appear to be located within the amygdala complex. More recently, we have provided evidence that manipulations of opiate and NE activity within the central nucleus region of the amygdala complex produce effects on the acquisition of classically conditioned heart rate in rabbits which closely parallel the effects of these same manipulations on retention of conditioning in rats. Basedon other lines of research which have provided evidence that opiate sensitive mechanisms located in the soma/dendritic and terminal fields of NE neurons are capable of alteraing brain NE function, the proposed research is designed to test the hypothesis that opiate sensitive mechanisms may alter learning and memory by regulating NE systems. To this end we propose to examine the effects of opiate manipulations on learning and memory in animals with selective NE system lesions. In addition, the possible contribution of vasopressin activity within the amygdala to these behavioral functions will also be examined. The behavioral testing procedures which will be used are those which wer have previously found to be sensitive to independent manipulation of opiate and NE activity within the amygdala. These are passive avoidance conditioning in rats, and classical conditioning of heart rate responding in rabbits. In addition to the proposed experiments, the applicant has included plans for research and professional development which involve collaboration and training with colleagues in both the Psychology Department and the Neurobiology Program at UNC, Chapel Hill.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Scientist Development Award - Research (K02)
Project #
5K02MH000406-05
Application #
3069759
Study Section
Research Scientist Development Review Committee (MHK)
Project Start
1982-07-01
Project End
1987-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
5
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
Schools of Arts and Sciences
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Holland, P C; Gallagher, M (1993) Amygdala central nucleus lesions disrupt increments, but not decrements, in conditioned stimulus processing. Behav Neurosci 107:246-53
Holland, P C; Gallagher, M (1993) Effects of amygdala central nucleus lesions on blocking and unblocking. Behav Neurosci 107:235-45
Gallagher, M; Holland, P C (1992) Preserved configural learning and spatial learning impairment in rats with hippocampal damage. Hippocampus 2:81-8
Hatfield, T; Graham, P W; Gallagher, M (1992) Taste-potentiated odor aversion learning: role of the amygdaloid basolateral complex and central nucleus. Behav Neurosci 106:286-93
Willner, J; Gallagher, M; Graham, P W et al. (1992) N-methyl-D-aspartate antagonist D-APV selectively disrupts taste-potentiated odor aversion learning. Behav Neurosci 106:315-23
Gallagher, M; Graham, P W; Holland, P C (1990) The amygdala central nucleus and appetitive Pavlovian conditioning: lesions impair one class of conditioned behavior. J Neurosci 10:1906-11
Gallagher, M; Burwell, R D (1989) Relationship of age-related decline across several behavioral domains. Neurobiol Aging 10:691-708
Jiang, H K; Owyang, V V; Hong, J S et al. (1989) Elevated dynorphin in the hippocampal formation of aged rats: relation to cognitive impairment on a spatial learning task. Proc Natl Acad Sci U S A 86:2948-51
Gallagher, M; Pelleymounter, M A (1988) An age-related spatial learning deficit: choline uptake distinguishes ""impaired"" and ""unimpaired"" rats. Neurobiol Aging 9:363-9
Decker, M W; Pelleymounter, M A; Gallagher, M (1988) Effects of training on a spatial memory task on high affinity choline uptake in hippocampus and cortex in young adult and aged rats. J Neurosci 8:90-9

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