The GABA- and dopaminergic (DA) neurons of the tubero-hypothalamic area and their target cells, the pituitary intermediate lobe (IL) melanotropes, will be used as a model system for the ontogeny of the mechanisms for neuronal co-transmitter control of endocrine cells. The concept of co- localization of multiple neurotransmitters within one neuron has become established through recent research. Co-localization adds a level of increased complexity to synaptic communication which is important to study to better comprehend neuronal regulation. Ontogenic studies unfold the processes by which a developing system forms and can explain the basis of the complexity of the mature system. The overall objective of this project is to link pre- and postsynaptic events during the ontogeny of the tubero-hypophysial system.
The specific aims are: (1) to establish the chronology of the development of the co- localization of GABA and DA in neurons of the tubero-hypothalamic area; (2) to define the time-sequence and spatial pattern of the GABA and DAergic innervation of the IL; (3) to establish the ontogeny of dopamine (d 2) and GABA receptors; and, (4) to study the impact of the event of innervation on IL melanotrope mitotic rate, pro-opiomelanocortin (POMC) gene expression, and secretory vesicle population. The techniques to be used include immunohistochemistry, immunocytochemistry, electron microscopic morphometry, in situ hybridization histochemistry, [3H]thymidine incorporation, and receptor binding assays. The significance of these studies relates to how co-localized neurotransmitters regulate their target cells. Understanding these regulatory mechanisms, which are unlikely to be unique to GABA/DA regulation of melanotropes, will allow the elucidation of more complex cellular communication systems. Comprehension of the mechanisms for co- transmitter action is a necessary step toward the design of therapeutic interventions to treat neurological disorders without adverse drug effects.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15NS028522-01
Application #
3440965
Study Section
Biochemical Endocrinology Study Section (BCE)
Project Start
1990-07-01
Project End
1993-12-31
Budget Start
1990-07-01
Budget End
1993-12-31
Support Year
1
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of Missouri Kansas City
Department
Type
Schools of Medicine
DUNS #
800772162
City
Kansas City
State
MO
Country
United States
Zip Code
64110