This research project seeks to extend our previous studies of hormonal control of neuronal development and function, which have been based on the Fundamental Hypothesis that gonadal steroids regulate the growth and development, and adult functional adaptability of peripheral sympathetic and parasympathetic neurons. Observations garnered steroids regulate neuropeptides in autonomic ganglia; gonadal steroids regulate neurotrophic factors in target organs of pelvic autonomic ganglia; and gonadal regulate the development of target organ innervation by autonomic neurons. The overall theme of these efforts is to establish a better understanding of the spectrum of hormonal influences on neuronal systems, and the mechanisms by which these steroid effects are mediated. The major questions to be asked include: 1) Does testosterone regulate the levels of mRNA for tyrosine hydroxylase (T-OH), T-OH enzyme protein, and T-OH activity in a specific manner? Will T-OH in situ hybridization permit identification of hormonal response patterns restricted to specific neurons in ganglia? Do hormones interact directly with the neuron? 2) Do hormones regulate neuropeptide Y (NPY) and vasoactive intestinal peptide (VIP) in pelvic ganglia? These two peptides are integrally involved in reproductive and excretory functions. 3) Are trophic molecules such as nerve growth factor (NGF) influenced by gonadal steroids, and do changes in the NGF receptor occur with hormonal pertubation? Do hormones exert their effects via target organs and the production of such trophic molecules? 4) Is the ability of the nerve to innervate target organs regulated by steroids? These studies will draw on multidisciplinary techniques including neurochemical, pharmacological, molecular biological, and tissue culture methods. Together these experiments should provide a detailed examination of the possible mechanisms by which steroids influence neuronal systems during development and adulthood. Thus, in a more general sense these studies should be relevant to issues of how the environmental milieu might influence the developing neuron and result in ontogenetic errors and defects. Since steroids may influence the aging process per se, our studies may have relevance from birth to senescence. Accordingly, the clinical relevance of these observation might include new understandings of birth defects, neurodegenerative disorders, neuroplasticity, and aging.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS022103-07
Application #
3404085
Study Section
Neurology C Study Section (NEUC)
Project Start
1986-12-01
Project End
1993-06-30
Budget Start
1992-12-01
Budget End
1993-06-30
Support Year
7
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Rochester
Department
Type
Schools of Dentistry
DUNS #
208469486
City
Rochester
State
NY
Country
United States
Zip Code
14627
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Romagnano, M A; Harshbarger, R J; Hamill, R W (1991) Brainstem enkephalinergic projections to spinal autonomic nuclei. J Neurosci 11:3539-55
Hamill, R W; Schroeder, B (1990) Hormonal regulation of adult sympathetic neurons: the effects of castration on neuropeptide Y, norepinephrine, and tyrosine hydroxylase activity. J Neurobiol 21:731-42
Melvin, J E; Hamill, R W (1989) Androgen-specific critical periods for the organization of the major pelvic ganglion. J Neurosci 9:736-42
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Dail, W G; Hamill, R W (1989) Parasympathetic nerves in penile erectile tissue of the rat contain choline acetyltransferase. Brain Res 487:165-70
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