The long-range goal of our research is to understand the mechanisms involved in the control of hormone secretion from the magnocellular neuroendocrine cells (MNCs) whose cell bodies reside predominantly in the supraoptic (SON) and paraventricular (PVN) nuclei of the hypothalamus. Since the patterns of electrical activity are dominant factors in the process of neurosecretion by these cells, our immediate goals for the research proposed here are to investigate some of the factors which may influence or determine their activity patterns. In particular we wish to focus on investigating membrane properties, synaptic inputs and non-synaptic interactions, all of which probably play roles in controlling or modulating the process of neurosecretion in this system. In order to accomplish these objectives, we will record intracellular from PVN and perifornical neurons and from both neurons and glial cells in the area of the SON in slices of rat hypothalamus. In some instances the electrodes will be filled with the fluorescent dye, Lucifer Yellow (LY), and in others with horseradish peroxidase (HRP) in order to identify the recorded cell and trace its processes. Cells marked with LY will undergo either subsequent immunocytochemical analysis of hormone content (oxytocin, vasopressin or enkephalin) or electron microscopic (EM) analysis to demonstrate gap junctions after rendering the LY electron dense. HRP-injected cells and their processes will be analyzed at both the light and EM levels in order to determine the collateral branching and axonal terminations of these neurons. Studies of putative transmitters will also be carried out. Thus, we will be able to determine the physiological, morphological and hormonal characteristics of cells in this brain area, as well as to learn more about the local circuitry in which these cell groups apparently participate.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS016942-11
Application #
3397247
Study Section
Neurology B Subcommittee 2 (NEUB)
Project Start
1981-01-01
Project End
1991-12-31
Budget Start
1991-01-01
Budget End
1991-12-31
Support Year
11
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Michigan State University
Department
Type
Schools of Arts and Sciences
DUNS #
193247145
City
East Lansing
State
MI
Country
United States
Zip Code
48824
Ponzio, Todd A; Hatton, Glenn I (2005) Adenosine postsynaptically modulates supraoptic neuronal excitability. J Neurophysiol 93:535-47
Hatton, Glenn I; Yang, Qin Zhao (2002) Synaptic potentials mediated by alpha 7 nicotinic acetylcholine receptors in supraoptic nucleus. J Neurosci 22:29-37
Hatton, Glenn I (2002) Glial-neuronal interactions in the mammalian brain. Adv Physiol Educ 26:225-37
Yang, Qin Zhao; Hatton, Glenn I (2002) Histamine H1-receptor modulation of inter-neuronal coupling among vasopressinergic neurons depends on nitric oxide synthase activation. Brain Res 955:115-22
Hatton, Glenn I; Zhao Yang, Qin (2002) Peripartum interneuronal coupling in the supraoptic nucleus. Brain Res 932:120-3
Hatton, G I; Yang, Q Z (2001) Ionotropic histamine receptors and H2 receptors modulate supraoptic oxytocin neuronal excitability and dye coupling. J Neurosci 21:2974-82
Li, Z; Hatton, G I (2000) Histamine suppresses non-NMDA excitatory synaptic currents in rat supraoptic nucleus neurons. J Neurophysiol 83:2616-25
Hatton, G I (1999) Astroglial modulation of neurotransmitter/peptide release from the neurohypophysis: present status. J Chem Neuroanat 16:203-21
Yang, Q Z; Hatton, G I (1999) Nitric oxide via cGMP-dependent mechanisms increases dye coupling and excitability of rat supraoptic nucleus neurons. J Neurosci 19:4270-9
Li, Z; Miyata, S; Hatton, G I (1999) Inositol 1,4,5-trisphosphate-sensitive Ca2+ stores in rat supraoptic neurons: involvement in histamine-induced enhancement of depolarizing afterpotentials. Neuroscience 93:667-74

Showing the most recent 10 out of 45 publications